{"id":9377,"date":"2021-01-05T22:43:35","date_gmt":"2021-01-06T03:43:35","guid":{"rendered":"https:\/\/nebula.org\/blog\/revue-genedx\/"},"modified":"2022-11-21T08:22:27","modified_gmt":"2022-11-21T13:22:27","slug":"revue-genedx","status":"publish","type":"post","link":"https:\/\/nebula.org\/blog\/fr\/revue-genedx\/","title":{"rendered":"Examen de GeneDx &#8211; Transformer les donn\u00e9es en diagnostic de maladies rares ?"},"content":{"rendered":"\n<div class=\"wp-block-uagb-review uagb-ratings__outer-wrap uagb-block-09105208\"><script type=\"application\/ld+json\">{\"@context\":\"https:\/\/schema.org\/\",\"@type\":\"Review\",\"reviewBody\":\"GeneDx is a clinical genomic testing company that offers FDA approved diagnostics. However, patients must go through physician and insurance payments that may get complicated. \",\"description\":\"GeneDx is a clinical genetic testing company that specializes is rare disease diagnostic. Learn more in our GeneDx review!\",\"itemReviewed\":{\"@type\":\"Product\",\"name\":\"&lt;strong>GeneDX Review Summary&lt;\/strong>\",\"description\":\"GeneDx is a clinical genetic testing company that specializes is rare disease diagnostic. Learn more in our GeneDx review!\",\"image\":\"https:\/\/nebula.org\/blog\/wp-content\/uploads\/2020\/10\/GeneDx-logo.png\",\"sku\":\"\",\"brand\":{\"@type\":\"Brand\",\"name\":\"GeneDx\"},\"offers\":{\"@type\":\"Offer\",\"price\":\"0\",\"url\":\"#\",\"priceValidUntil\":\"2024-12-19T00:00:00\",\"priceCurrency\":\"USD\",\"availability\":\"https:\/\/schema.org\/InStock\"},\"gtin\":\"\"},\"reviewRating\":{\"@type\":\"Rating\",\"ratingValue\":4.5,\"worstRating\":\"0\",\"bestRating\":5},\"author\":{\"@type\":\"Person\",\"name\":\"Nikki Teran\"},\"publisher\":\"Nebula Genomics\",\"datePublished\":\"2022-09-09T00:00:00\",\"url\":\"#\"}<\/script><div class=\"uagb_review_block\"><a href=\"#\" class=\"uagb-rating-link-wrapper\" target=\"\" rel=\"noopener noreferrer\"><h2 class=\"uagb-rating-title\"><strong>R\u00e9sum\u00e9 de l&rsquo;examen de GeneDX<\/strong><\/h2><\/a><p class=\"uagb-rating-desc\">GeneDx est une soci\u00e9t\u00e9 de tests g\u00e9n\u00e9tiques cliniques sp\u00e9cialis\u00e9e dans le diagnostic des maladies rares. Apprenez-en plus dans notre revue GeneDx!<\/p><p class=\"uagb-rating-author\">Nikki Teran<\/p><div class=\"uagb-rating__source-wrap\"><img decoding=\"async\" class=\"uagb-howto__source-image\" src=\"https:\/\/nebula.org\/blog\/wp-content\/uploads\/2020\/10\/GeneDx-logo-300x108.png\" title=\"Logo GeneDx\" alt=\"Logo GeneDx\"><\/div><div class=\"uagb_review_entry\"><div>R\u00e9sultats<\/div><div style=\"margin-left:auto;min-width:120px\"><div style=\"display:flex;flex-direction:flex-row\"><svg xmlns=\"https:\/\/www.w3.org\/2000\/svg\" height=\"20\" width=\"20\" viewbox=\"0 0 150 150\"><defs><mask id=\"uagb_review_star_filter-09105208-0-0\"><rect height=\"150\" width=\"150\" y=\"0\" x=\"0\" fill=\"#fff\"\/><\/mask><\/defs><path fill=\"#888888\" stroke-width=\"2.5\" d=\"m0.75,56.89914l56.02207,0l17.31126,-56.14914l17.31126,56.14914l56.02206,0l-45.32273,34.70168l17.31215,56.14914l-45.32274,-34.70262l-45.32274,34.70262l17.31215,-56.14914l-45.32274,-34.70168z\" stroke=\"#000000\"><\/path><path class=\"star\" id=\"star0\" mask=\"url(#uagb_review_star_filter-09105208-0-0)\" fill=\"#eeee00\" stroke-width=\"2.5\" d=\"m0.75,56.89914l56.02207,0l17.31126,-56.14914l17.31126,56.14914l56.02206,0l-45.32273,34.70168l17.31215,56.14914l-45.32274,-34.70262l-45.32274,34.70262l17.31215,-56.14914l-45.32274,-34.70168z\" stroke=\"#000000\"><\/path><\/path><\/path><\/svg><svg xmlns=\"https:\/\/www.w3.org\/2000\/svg\" height=\"20\" width=\"20\" viewbox=\"0 0 150 150\"><defs><mask id=\"uagb_review_star_filter-09105208-0-1\"><rect height=\"150\" width=\"150\" y=\"0\" x=\"0\" fill=\"#fff\"\/><\/mask><\/defs><path fill=\"#888888\" stroke-width=\"2.5\" d=\"m0.75,56.89914l56.02207,0l17.31126,-56.14914l17.31126,56.14914l56.02206,0l-45.32273,34.70168l17.31215,56.14914l-45.32274,-34.70262l-45.32274,34.70262l17.31215,-56.14914l-45.32274,-34.70168z\" stroke=\"#000000\"><\/path><path class=\"star\" id=\"star1\" mask=\"url(#uagb_review_star_filter-09105208-0-1)\" fill=\"#eeee00\" stroke-width=\"2.5\" d=\"m0.75,56.89914l56.02207,0l17.31126,-56.14914l17.31126,56.14914l56.02206,0l-45.32273,34.70168l17.31215,56.14914l-45.32274,-34.70262l-45.32274,34.70262l17.31215,-56.14914l-45.32274,-34.70168z\" stroke=\"#000000\"><\/path><\/path><\/path><\/svg><svg xmlns=\"https:\/\/www.w3.org\/2000\/svg\" height=\"20\" width=\"20\" viewbox=\"0 0 150 150\"><defs><mask id=\"uagb_review_star_filter-09105208-0-2\"><rect height=\"150\" width=\"150\" y=\"0\" x=\"0\" fill=\"#fff\"\/><\/mask><\/defs><path fill=\"#888888\" stroke-width=\"2.5\" d=\"m0.75,56.89914l56.02207,0l17.31126,-56.14914l17.31126,56.14914l56.02206,0l-45.32273,34.70168l17.31215,56.14914l-45.32274,-34.70262l-45.32274,34.70262l17.31215,-56.14914l-45.32274,-34.70168z\" stroke=\"#000000\"><\/path><path class=\"star\" id=\"star2\" mask=\"url(#uagb_review_star_filter-09105208-0-2)\" fill=\"#eeee00\" stroke-width=\"2.5\" d=\"m0.75,56.89914l56.02207,0l17.31126,-56.14914l17.31126,56.14914l56.02206,0l-45.32273,34.70168l17.31215,56.14914l-45.32274,-34.70262l-45.32274,34.70262l17.31215,-56.14914l-45.32274,-34.70168z\" stroke=\"#000000\"><\/path><\/path><\/path><\/svg><svg xmlns=\"https:\/\/www.w3.org\/2000\/svg\" height=\"20\" width=\"20\" viewbox=\"0 0 150 150\"><defs><mask id=\"uagb_review_star_filter-09105208-0-3\"><rect height=\"150\" width=\"150\" y=\"0\" x=\"0\" fill=\"#fff\"\/><\/mask><\/defs><path fill=\"#888888\" stroke-width=\"2.5\" d=\"m0.75,56.89914l56.02207,0l17.31126,-56.14914l17.31126,56.14914l56.02206,0l-45.32273,34.70168l17.31215,56.14914l-45.32274,-34.70262l-45.32274,34.70262l17.31215,-56.14914l-45.32274,-34.70168z\" stroke=\"#000000\"><\/path><path class=\"star\" id=\"star3\" mask=\"url(#uagb_review_star_filter-09105208-0-3)\" fill=\"#eeee00\" stroke-width=\"2.5\" d=\"m0.75,56.89914l56.02207,0l17.31126,-56.14914l17.31126,56.14914l56.02206,0l-45.32273,34.70168l17.31215,56.14914l-45.32274,-34.70262l-45.32274,34.70262l17.31215,-56.14914l-45.32274,-34.70168z\" stroke=\"#000000\"><\/path><\/path><\/path><\/svg><svg xmlns=\"https:\/\/www.w3.org\/2000\/svg\" height=\"20\" width=\"20\" viewbox=\"0 0 150 150\"><defs><mask id=\"uagb_review_star_filter-09105208-0-4\"><rect height=\"150\" width=\"150\" y=\"0\" x=\"0\" fill=\"#fff\"\/><\/mask><\/defs><path fill=\"#888888\" stroke-width=\"2.5\" d=\"m0.75,56.89914l56.02207,0l17.31126,-56.14914l17.31126,56.14914l56.02206,0l-45.32273,34.70168l17.31215,56.14914l-45.32274,-34.70262l-45.32274,34.70262l17.31215,-56.14914l-45.32274,-34.70168z\" stroke=\"#000000\"><\/path><path class=\"star\" id=\"star4\" mask=\"url(#uagb_review_star_filter-09105208-0-4)\" fill=\"#eeee00\" stroke-width=\"2.5\" d=\"m0.75,56.89914l56.02207,0l17.31126,-56.14914l17.31126,56.14914l56.02206,0l-45.32273,34.70168l17.31215,56.14914l-45.32274,-34.70262l-45.32274,34.70262l17.31215,-56.14914l-45.32274,-34.70168z\" stroke=\"#000000\"><\/path><\/path><\/path><\/svg><\/div><\/div><\/div><div class=\"uagb_review_entry\"><div>Prix<\/div><div style=\"margin-left:auto;min-width:120px\"><div style=\"display:flex;flex-direction:flex-row\"><svg xmlns=\"https:\/\/www.w3.org\/2000\/svg\" height=\"20\" width=\"20\" viewbox=\"0 0 150 150\"><defs><mask id=\"uagb_review_star_filter-09105208-1-0\"><rect height=\"150\" width=\"150\" y=\"0\" x=\"0\" fill=\"#fff\"\/><\/mask><\/defs><path fill=\"#888888\" stroke-width=\"2.5\" d=\"m0.75,56.89914l56.02207,0l17.31126,-56.14914l17.31126,56.14914l56.02206,0l-45.32273,34.70168l17.31215,56.14914l-45.32274,-34.70262l-45.32274,34.70262l17.31215,-56.14914l-45.32274,-34.70168z\" stroke=\"#000000\"><\/path><path class=\"star\" id=\"star0\" mask=\"url(#uagb_review_star_filter-09105208-1-0)\" fill=\"#eeee00\" stroke-width=\"2.5\" d=\"m0.75,56.89914l56.02207,0l17.31126,-56.14914l17.31126,56.14914l56.02206,0l-45.32273,34.70168l17.31215,56.14914l-45.32274,-34.70262l-45.32274,34.70262l17.31215,-56.14914l-45.32274,-34.70168z\" stroke=\"#000000\"><\/path><\/path><\/path><\/svg><svg xmlns=\"https:\/\/www.w3.org\/2000\/svg\" height=\"20\" width=\"20\" viewbox=\"0 0 150 150\"><defs><mask id=\"uagb_review_star_filter-09105208-1-1\"><rect height=\"150\" width=\"150\" y=\"0\" x=\"0\" fill=\"#fff\"\/><\/mask><\/defs><path fill=\"#888888\" stroke-width=\"2.5\" d=\"m0.75,56.89914l56.02207,0l17.31126,-56.14914l17.31126,56.14914l56.02206,0l-45.32273,34.70168l17.31215,56.14914l-45.32274,-34.70262l-45.32274,34.70262l17.31215,-56.14914l-45.32274,-34.70168z\" stroke=\"#000000\"><\/path><path class=\"star\" id=\"star1\" mask=\"url(#uagb_review_star_filter-09105208-1-1)\" fill=\"#eeee00\" stroke-width=\"2.5\" d=\"m0.75,56.89914l56.02207,0l17.31126,-56.14914l17.31126,56.14914l56.02206,0l-45.32273,34.70168l17.31215,56.14914l-45.32274,-34.70262l-45.32274,34.70262l17.31215,-56.14914l-45.32274,-34.70168z\" stroke=\"#000000\"><\/path><\/path><\/path><\/svg><svg xmlns=\"https:\/\/www.w3.org\/2000\/svg\" height=\"20\" width=\"20\" viewbox=\"0 0 150 150\"><defs><mask id=\"uagb_review_star_filter-09105208-1-2\"><rect height=\"150\" width=\"150\" y=\"0\" x=\"0\" fill=\"#fff\"\/><\/mask><\/defs><path fill=\"#888888\" stroke-width=\"2.5\" d=\"m0.75,56.89914l56.02207,0l17.31126,-56.14914l17.31126,56.14914l56.02206,0l-45.32273,34.70168l17.31215,56.14914l-45.32274,-34.70262l-45.32274,34.70262l17.31215,-56.14914l-45.32274,-34.70168z\" stroke=\"#000000\"><\/path><path class=\"star\" id=\"star2\" mask=\"url(#uagb_review_star_filter-09105208-1-2)\" fill=\"#eeee00\" stroke-width=\"2.5\" d=\"m0.75,56.89914l56.02207,0l17.31126,-56.14914l17.31126,56.14914l56.02206,0l-45.32273,34.70168l17.31215,56.14914l-45.32274,-34.70262l-45.32274,34.70262l17.31215,-56.14914l-45.32274,-34.70168z\" stroke=\"#000000\"><\/path><\/path><\/path><\/svg><svg xmlns=\"https:\/\/www.w3.org\/2000\/svg\" height=\"20\" width=\"20\" viewbox=\"0 0 150 150\"><defs><mask id=\"uagb_review_star_filter-09105208-1-3\"><rect height=\"150\" width=\"150\" y=\"0\" x=\"0\" fill=\"#fff\"\/><\/mask><\/defs><path fill=\"#888888\" stroke-width=\"2.5\" d=\"m0.75,56.89914l56.02207,0l17.31126,-56.14914l17.31126,56.14914l56.02206,0l-45.32273,34.70168l17.31215,56.14914l-45.32274,-34.70262l-45.32274,34.70262l17.31215,-56.14914l-45.32274,-34.70168z\" stroke=\"#000000\"><\/path><path class=\"star\" id=\"star3\" mask=\"url(#uagb_review_star_filter-09105208-1-3)\" fill=\"#eeee00\" stroke-width=\"2.5\" d=\"m0.75,56.89914l56.02207,0l17.31126,-56.14914l17.31126,56.14914l56.02206,0l-45.32273,34.70168l17.31215,56.14914l-45.32274,-34.70262l-45.32274,34.70262l17.31215,-56.14914l-45.32274,-34.70168z\" stroke=\"#000000\"><\/path><\/path><\/path><\/svg><svg xmlns=\"https:\/\/www.w3.org\/2000\/svg\" height=\"20\" width=\"20\" viewbox=\"0 0 150 150\"><defs><mask id=\"uagb_review_star_filter-09105208-1-4\"><rect height=\"150\" width=\"75\" y=\"0\" x=\"0\" fill=\"#fff\"\/><\/mask><\/defs><path fill=\"#888888\" stroke-width=\"2.5\" d=\"m0.75,56.89914l56.02207,0l17.31126,-56.14914l17.31126,56.14914l56.02206,0l-45.32273,34.70168l17.31215,56.14914l-45.32274,-34.70262l-45.32274,34.70262l17.31215,-56.14914l-45.32274,-34.70168z\" stroke=\"#000000\"><\/path><path class=\"star\" id=\"star4\" mask=\"url(#uagb_review_star_filter-09105208-1-4)\" fill=\"#eeee00\" stroke-width=\"2.5\" d=\"m0.75,56.89914l56.02207,0l17.31126,-56.14914l17.31126,56.14914l56.02206,0l-45.32273,34.70168l17.31215,56.14914l-45.32274,-34.70262l-45.32274,34.70262l17.31215,-56.14914l-45.32274,-34.70168z\" stroke=\"#000000\"><\/path><\/path><\/path><\/svg><\/div><\/div><\/div><div class=\"uagb_review_entry\"><div>Facilit\u00e9 d&rsquo;utilisation<\/div><div style=\"margin-left:auto;min-width:120px\"><div style=\"display:flex;flex-direction:flex-row\"><svg xmlns=\"https:\/\/www.w3.org\/2000\/svg\" height=\"20\" width=\"20\" viewbox=\"0 0 150 150\"><defs><mask id=\"uagb_review_star_filter-09105208-2-0\"><rect height=\"150\" width=\"150\" y=\"0\" x=\"0\" fill=\"#fff\"\/><\/mask><\/defs><path fill=\"#888888\" stroke-width=\"2.5\" d=\"m0.75,56.89914l56.02207,0l17.31126,-56.14914l17.31126,56.14914l56.02206,0l-45.32273,34.70168l17.31215,56.14914l-45.32274,-34.70262l-45.32274,34.70262l17.31215,-56.14914l-45.32274,-34.70168z\" stroke=\"#000000\"><\/path><path class=\"star\" id=\"star0\" mask=\"url(#uagb_review_star_filter-09105208-2-0)\" fill=\"#eeee00\" stroke-width=\"2.5\" d=\"m0.75,56.89914l56.02207,0l17.31126,-56.14914l17.31126,56.14914l56.02206,0l-45.32273,34.70168l17.31215,56.14914l-45.32274,-34.70262l-45.32274,34.70262l17.31215,-56.14914l-45.32274,-34.70168z\" stroke=\"#000000\"><\/path><\/path><\/path><\/svg><svg xmlns=\"https:\/\/www.w3.org\/2000\/svg\" height=\"20\" width=\"20\" viewbox=\"0 0 150 150\"><defs><mask id=\"uagb_review_star_filter-09105208-2-1\"><rect height=\"150\" width=\"150\" y=\"0\" x=\"0\" fill=\"#fff\"\/><\/mask><\/defs><path fill=\"#888888\" stroke-width=\"2.5\" d=\"m0.75,56.89914l56.02207,0l17.31126,-56.14914l17.31126,56.14914l56.02206,0l-45.32273,34.70168l17.31215,56.14914l-45.32274,-34.70262l-45.32274,34.70262l17.31215,-56.14914l-45.32274,-34.70168z\" stroke=\"#000000\"><\/path><path class=\"star\" id=\"star1\" mask=\"url(#uagb_review_star_filter-09105208-2-1)\" fill=\"#eeee00\" stroke-width=\"2.5\" d=\"m0.75,56.89914l56.02207,0l17.31126,-56.14914l17.31126,56.14914l56.02206,0l-45.32273,34.70168l17.31215,56.14914l-45.32274,-34.70262l-45.32274,34.70262l17.31215,-56.14914l-45.32274,-34.70168z\" stroke=\"#000000\"><\/path><\/path><\/path><\/svg><svg xmlns=\"https:\/\/www.w3.org\/2000\/svg\" height=\"20\" width=\"20\" viewbox=\"0 0 150 150\"><defs><mask id=\"uagb_review_star_filter-09105208-2-2\"><rect height=\"150\" width=\"150\" y=\"0\" x=\"0\" fill=\"#fff\"\/><\/mask><\/defs><path fill=\"#888888\" stroke-width=\"2.5\" d=\"m0.75,56.89914l56.02207,0l17.31126,-56.14914l17.31126,56.14914l56.02206,0l-45.32273,34.70168l17.31215,56.14914l-45.32274,-34.70262l-45.32274,34.70262l17.31215,-56.14914l-45.32274,-34.70168z\" stroke=\"#000000\"><\/path><path class=\"star\" id=\"star2\" mask=\"url(#uagb_review_star_filter-09105208-2-2)\" fill=\"#eeee00\" stroke-width=\"2.5\" d=\"m0.75,56.89914l56.02207,0l17.31126,-56.14914l17.31126,56.14914l56.02206,0l-45.32273,34.70168l17.31215,56.14914l-45.32274,-34.70262l-45.32274,34.70262l17.31215,-56.14914l-45.32274,-34.70168z\" stroke=\"#000000\"><\/path><\/path><\/path><\/svg><svg xmlns=\"https:\/\/www.w3.org\/2000\/svg\" height=\"20\" width=\"20\" viewbox=\"0 0 150 150\"><defs><mask id=\"uagb_review_star_filter-09105208-2-3\"><rect height=\"150\" width=\"150\" y=\"0\" x=\"0\" fill=\"#fff\"\/><\/mask><\/defs><path fill=\"#888888\" stroke-width=\"2.5\" d=\"m0.75,56.89914l56.02207,0l17.31126,-56.14914l17.31126,56.14914l56.02206,0l-45.32273,34.70168l17.31215,56.14914l-45.32274,-34.70262l-45.32274,34.70262l17.31215,-56.14914l-45.32274,-34.70168z\" stroke=\"#000000\"><\/path><path class=\"star\" id=\"star3\" mask=\"url(#uagb_review_star_filter-09105208-2-3)\" fill=\"#eeee00\" stroke-width=\"2.5\" d=\"m0.75,56.89914l56.02207,0l17.31126,-56.14914l17.31126,56.14914l56.02206,0l-45.32273,34.70168l17.31215,56.14914l-45.32274,-34.70262l-45.32274,34.70262l17.31215,-56.14914l-45.32274,-34.70168z\" stroke=\"#000000\"><\/path><\/path><\/path><\/svg><svg xmlns=\"https:\/\/www.w3.org\/2000\/svg\" height=\"20\" width=\"20\" viewbox=\"0 0 150 150\"><defs><mask id=\"uagb_review_star_filter-09105208-2-4\"><rect height=\"150\" width=\"0\" y=\"0\" x=\"0\" fill=\"#fff\"\/><\/mask><\/defs><path fill=\"#888888\" stroke-width=\"2.5\" d=\"m0.75,56.89914l56.02207,0l17.31126,-56.14914l17.31126,56.14914l56.02206,0l-45.32273,34.70168l17.31215,56.14914l-45.32274,-34.70262l-45.32274,34.70262l17.31215,-56.14914l-45.32274,-34.70168z\" stroke=\"#000000\"><\/path><path class=\"star\" id=\"star4\" mask=\"url(#uagb_review_star_filter-09105208-2-4)\" fill=\"#eeee00\" stroke-width=\"2.5\" d=\"m0.75,56.89914l56.02207,0l17.31126,-56.14914l17.31126,56.14914l56.02206,0l-45.32273,34.70168l17.31215,56.14914l-45.32274,-34.70262l-45.32274,34.70262l17.31215,-56.14914l-45.32274,-34.70168z\" stroke=\"#000000\"><\/path><\/path><\/path><\/svg><\/div><\/div><\/div><div class=\"uagb_review_summary\"><p class=\"uagb_review_summary_title\">Sommaire<\/p><div class=\"uagb_review_overall_value\"><p class=\"uagb_review_summary_desc\">GeneDx est une soci\u00e9t\u00e9 de tests g\u00e9nomiques cliniques qui propose des diagnostics approuv\u00e9s par la FDA. Cependant, les patients doivent passer par les paiements des m\u00e9decins et des assurances, ce qui peut s&rsquo;av\u00e9rer compliqu\u00e9.  <\/p><div class=\"uagb_review_average\"><span class=\"uagb_review_rating\">4.5<\/span><div class=\"uagb_review_average_stars\" style=\"display:flex;flex-direction:flex-row\"><svg xmlns=\"https:\/\/www.w3.org\/2000\/svg\" height=\"20\" width=\"20\" viewbox=\"0 0 150 150\"><defs><mask id=\"uagb_review_star_filter-09105208-average-0\"><rect height=\"150\" width=\"150\" y=\"0\" x=\"0\" fill=\"#fff\"\/><\/mask><\/defs><path fill=\"#888888\" stroke-width=\"2.5\" d=\"m0.75,56.89914l56.02207,0l17.31126,-56.14914l17.31126,56.14914l56.02206,0l-45.32273,34.70168l17.31215,56.14914l-45.32274,-34.70262l-45.32274,34.70262l17.31215,-56.14914l-45.32274,-34.70168z\" stroke=\"#000000\"><\/path><path class=\"star\" id=\"star0\" mask=\"url(#uagb_review_star_filter-09105208-average-0)\" fill=\"#eeee00\" stroke-width=\"2.5\" d=\"m0.75,56.89914l56.02207,0l17.31126,-56.14914l17.31126,56.14914l56.02206,0l-45.32273,34.70168l17.31215,56.14914l-45.32274,-34.70262l-45.32274,34.70262l17.31215,-56.14914l-45.32274,-34.70168z\" stroke=\"#000000\"><\/path><\/path><\/path><\/svg><svg xmlns=\"https:\/\/www.w3.org\/2000\/svg\" height=\"20\" width=\"20\" viewbox=\"0 0 150 150\"><defs><mask id=\"uagb_review_star_filter-09105208-average-1\"><rect height=\"150\" width=\"150\" y=\"0\" x=\"0\" fill=\"#fff\"\/><\/mask><\/defs><path fill=\"#888888\" stroke-width=\"2.5\" d=\"m0.75,56.89914l56.02207,0l17.31126,-56.14914l17.31126,56.14914l56.02206,0l-45.32273,34.70168l17.31215,56.14914l-45.32274,-34.70262l-45.32274,34.70262l17.31215,-56.14914l-45.32274,-34.70168z\" stroke=\"#000000\"><\/path><path class=\"star\" id=\"star1\" mask=\"url(#uagb_review_star_filter-09105208-average-1)\" fill=\"#eeee00\" stroke-width=\"2.5\" d=\"m0.75,56.89914l56.02207,0l17.31126,-56.14914l17.31126,56.14914l56.02206,0l-45.32273,34.70168l17.31215,56.14914l-45.32274,-34.70262l-45.32274,34.70262l17.31215,-56.14914l-45.32274,-34.70168z\" stroke=\"#000000\"><\/path><\/path><\/path><\/svg><svg xmlns=\"https:\/\/www.w3.org\/2000\/svg\" height=\"20\" width=\"20\" viewbox=\"0 0 150 150\"><defs><mask id=\"uagb_review_star_filter-09105208-average-2\"><rect height=\"150\" width=\"150\" y=\"0\" x=\"0\" fill=\"#fff\"\/><\/mask><\/defs><path fill=\"#888888\" stroke-width=\"2.5\" d=\"m0.75,56.89914l56.02207,0l17.31126,-56.14914l17.31126,56.14914l56.02206,0l-45.32273,34.70168l17.31215,56.14914l-45.32274,-34.70262l-45.32274,34.70262l17.31215,-56.14914l-45.32274,-34.70168z\" stroke=\"#000000\"><\/path><path class=\"star\" id=\"star2\" mask=\"url(#uagb_review_star_filter-09105208-average-2)\" fill=\"#eeee00\" stroke-width=\"2.5\" d=\"m0.75,56.89914l56.02207,0l17.31126,-56.14914l17.31126,56.14914l56.02206,0l-45.32273,34.70168l17.31215,56.14914l-45.32274,-34.70262l-45.32274,34.70262l17.31215,-56.14914l-45.32274,-34.70168z\" stroke=\"#000000\"><\/path><\/path><\/path><\/svg><svg xmlns=\"https:\/\/www.w3.org\/2000\/svg\" height=\"20\" width=\"20\" viewbox=\"0 0 150 150\"><defs><mask id=\"uagb_review_star_filter-09105208-average-3\"><rect height=\"150\" width=\"150\" y=\"0\" x=\"0\" fill=\"#fff\"\/><\/mask><\/defs><path fill=\"#888888\" stroke-width=\"2.5\" d=\"m0.75,56.89914l56.02207,0l17.31126,-56.14914l17.31126,56.14914l56.02206,0l-45.32273,34.70168l17.31215,56.14914l-45.32274,-34.70262l-45.32274,34.70262l17.31215,-56.14914l-45.32274,-34.70168z\" stroke=\"#000000\"><\/path><path class=\"star\" id=\"star3\" mask=\"url(#uagb_review_star_filter-09105208-average-3)\" fill=\"#eeee00\" stroke-width=\"2.5\" d=\"m0.75,56.89914l56.02207,0l17.31126,-56.14914l17.31126,56.14914l56.02206,0l-45.32273,34.70168l17.31215,56.14914l-45.32274,-34.70262l-45.32274,34.70262l17.31215,-56.14914l-45.32274,-34.70168z\" stroke=\"#000000\"><\/path><\/path><\/path><\/svg><svg xmlns=\"https:\/\/www.w3.org\/2000\/svg\" height=\"20\" width=\"20\" viewbox=\"0 0 150 150\"><defs><mask id=\"uagb_review_star_filter-09105208-average-4\"><rect height=\"150\" width=\"75\" y=\"0\" x=\"0\" fill=\"#fff\"\/><\/mask><\/defs><path fill=\"#888888\" stroke-width=\"2.5\" d=\"m0.75,56.89914l56.02207,0l17.31126,-56.14914l17.31126,56.14914l56.02206,0l-45.32273,34.70168l17.31215,56.14914l-45.32274,-34.70262l-45.32274,34.70262l17.31215,-56.14914l-45.32274,-34.70168z\" stroke=\"#000000\"><\/path><path class=\"star\" id=\"star4\" mask=\"url(#uagb_review_star_filter-09105208-average-4)\" fill=\"#eeee00\" stroke-width=\"2.5\" d=\"m0.75,56.89914l56.02207,0l17.31126,-56.14914l17.31126,56.14914l56.02206,0l-45.32273,34.70168l17.31215,56.14914l-45.32274,-34.70262l-45.32274,34.70262l17.31215,-56.14914l-45.32274,-34.70168z\" stroke=\"#000000\"><\/path><\/path><\/path><\/svg><\/div><\/div><\/div><\/div><\/div><\/div>\n\n<h2 class=\"wp-block-heading\" id=\"h-7-facts-from-our-genedx-review\"><strong>7 faits tir\u00e9s de notre examen de GeneDx<\/strong><\/h2>\n\n<ol class=\"wp-block-list\"><li><strong>Emplacement:<\/strong> Gaithersburg, Maryland<\/li><li><strong>Produits : <\/strong>Grande vari\u00e9t\u00e9 de tests g\u00e9nomiques cliniques, g\u00e9n\u00e9tique m\u00e9dicale sur les troubles g\u00e9n\u00e9tiques rares.<\/li><li><strong>Rapports :<\/strong> Rapports de sant\u00e9 d\u00e9taill\u00e9s pour des conditions g\u00e9n\u00e9tiques sp\u00e9cifiques<\/li><li><strong>Livraison du r\u00e9sultat : <\/strong>Jusqu&rsquo;\u00e0 16 semaines<\/li><li><strong>Confidentialit\u00e9 : <\/strong>Transmet des donn\u00e9es anonymes \u00e0 ClinVar<\/li><li><strong>Co\u00fbt : <\/strong>Tr\u00e8s variable, mais peut \u00eatre couvert par une assurance.<\/li><li><strong>Alternatives : <\/strong><a href=\"https:\/\/nebula.org\/whole-genome-sequencing\/\">Nebula Genomics (s\u00e9quen\u00e7age du g\u00e9nome entier avec rapports r\u00e9guli\u00e8rement mis \u00e0 jour)<\/a><\/li><\/ol>\n\n<p>Cette critique est \u00e9crite avec l&rsquo;intention d&rsquo;\u00eatre aussi impartiale que possible. Cependant, il repr\u00e9sente l&rsquo;opinion d&rsquo;un \u00e9valuateur individuel et est donc subjectif. De plus, chez Nebula Genomics, nous cherchons \u00e0 \u00e9duquer le public sur les avantages du s\u00e9quen\u00e7age du g\u00e9nome entier. Des informations sur notre test ADN de s\u00e9quen\u00e7age du g\u00e9nome entier sont donc int\u00e9gr\u00e9es \u00e0 l&rsquo;examen.<\/p>\n\n<p class=\"has-medium-font-size\">9 septembre 2022<\/p>\n\n<div class=\"wp-block-yoast-seo-table-of-contents yoast-table-of-contents\"><h2>Table des mati\u00e8res<\/h2><ul><li><a href=\"#h-7-facts-from-our-genedx-review\" data-level=\"2\">7 faits tir\u00e9s de notre examen de GeneDx<\/a><\/li><li><a href=\"#h-pros-and-cons\" data-level=\"2\">Avantages et inconv\u00e9nients<\/a><ul><li><a href=\"#h-pros\" data-level=\"3\">Avantages<\/a><\/li><li><a href=\"#h-cons\" data-level=\"3\">Les inconv\u00e9nients<\/a><\/li><\/ul><\/li><li><a href=\"#h-introduction\" data-level=\"2\">introduction<\/a><\/li><li><a href=\"#h-company-overview\" data-level=\"2\">Pr\u00e9sentation de l&rsquo;entreprise<\/a><\/li><li><a href=\"#h-review-of-how-genedx-works\" data-level=\"2\">Examen du fonctionnement de GeneDx<\/a><\/li><li><a href=\"#h-review-of-a-genedx-sample-report\" data-level=\"2\">Examen d&rsquo;un \u00e9chantillon de rapport GeneDx<\/a><\/li><li><a href=\"#h-review-of-genedx-clinician-oversight\" data-level=\"2\">Examen de la surveillance des cliniciens de GeneDx<\/a><\/li><li><a href=\"#h-review-of-genedx-costs\" data-level=\"2\">Examen des co\u00fbts de GeneDx<\/a><\/li><li><a href=\"#h-review-of-genedx-privacy\" data-level=\"2\">Examen de la confidentialit\u00e9 de GeneDx<\/a><\/li><li><a href=\"#h-genedx-in-the-news\" data-level=\"2\">GeneDx dans la presse<\/a><\/li><li><a href=\"#h-other-genedx-reviews\" data-level=\"2\">Autres avis sur GeneDx<\/a><\/li><li><a href=\"#h-nebula-genomics\" data-level=\"2\">G\u00e9nomique des n\u00e9buleuses<\/a><ul><li><a href=\"#h-30x-whole-genome-sequencing\" data-level=\"3\">S\u00e9quen\u00e7age du g\u00e9nome entier 30x<\/a><\/li><li><a href=\"#h-nebula-empowers-the-user-to-learn-about-their-own-dna\" data-level=\"3\">Nebula permet \u00e0 l&rsquo;utilisateur de d\u00e9couvrir son propre ADN<\/a><\/li><\/ul><\/li><\/ul><\/div>\n\n<h2 class=\"wp-block-heading\" id=\"h-pros-and-cons\"><strong>Avantages et inconv\u00e9nients<\/strong><\/h2>\n\n<h3 class=\"wp-block-heading\" id=\"h-pros\">Avantages<\/h3>\n\n<ul class=\"wp-block-list\"><li>Tests de diagnostic approuv\u00e9s par la FDA pour de nombreuses maladies rares<\/li><li>Sous contrat avec la plupart des principales assurances<\/li><\/ul>\n\n<h3 class=\"wp-block-heading\" id=\"h-cons\">Les inconv\u00e9nients<\/h3>\n\n<ul class=\"wp-block-list\"><li>Pas d&rsquo;\u00e9ducation directe des patients<\/li><li>Retour lent des r\u00e9sultats<\/li><li>Probl\u00e8mes d&rsquo;assurance et facturation inattendue<\/li><\/ul>\n\n<h2 class=\"wp-block-heading\" id=\"h-introduction\"><strong>introduction<\/strong><\/h2>\n\n<p>GeneDx est une entreprise de g\u00e9nomique clinique situ\u00e9e \u00e0 Gaithersburg, dans le Maryland, qui se concentre sur le diagnostic des maladies rares et ultra-rare. L&rsquo;entreprise fait partie de BioReference Laboratories, Inc, une soci\u00e9t\u00e9 d&rsquo;OPKO Health. Les tests d&rsquo;hybridation ou de s\u00e9quen\u00e7age de la prochaine g\u00e9n\u00e9ration doivent \u00eatre command\u00e9s par un m\u00e9decin, un DO ou, dans certains \u00c9tats, un <a href=\"https:\/\/nebula.org\/blog\/fr\/genetic-counseling-2\/\">conseiller en g\u00e9n\u00e9tique<\/a>. Ensuite, ces r\u00e9sultats sont renvoy\u00e9s directement au professionnel de la sant\u00e9.<\/p>\n\n<p>GeneDx propose les r\u00e9sultats de ses tests en tant qu&rsquo;informations sur les actions \u00e0 mener par les patients. Selon le site, GeneDx est un leader mondial de la g\u00e9nomique, avec un syst\u00e8me complet de tests g\u00e9n\u00e9tiques GeneDx. Mais de nombreux avis d&rsquo;utilisateurs se plaignent des co\u00fbts \u00e9lev\u00e9s. <\/p>\n\n<p>De nombreuses compagnies d&rsquo;assurance nationales couvrent ses tests approuv\u00e9s par la FDA, mais les frais \u00e0 payer peuvent varier.  <\/p>\n\n<figure class=\"wp-block-table is-style-regular\"><table class=\"has-background\" style=\"background-color:#fcf0ef\"><tbody><tr><td><strong><a href=\"https:\/\/nebula.org\/whole-genome-sequencing\/\">\u00cates-vous int\u00e9ress\u00e9 par un test qui d\u00e9code 100% de votre ADN au lieu de quelques g\u00e8nes seulement ? <\/a><\/strong><br\/><br\/><strong><a href=\"https:\/\/nebula.org\/whole-genome-sequencing\/\">Nebula Genomics offre un s\u00e9quen\u00e7age du g\u00e9nome entier \u00e0 un prix abordable ! Ce test ADN complet traduit l&rsquo;ensemble des 20 000 g\u00e8nes et r\u00e9gions g\u00e9nomiques r\u00e9gulatrices.  <\/a><\/strong><br\/><br\/><strong><a href=\"https:\/\/nebula.org\/whole-genome-sequencing\/\">En comparaison, GeneDx ne s\u00e9quence que quelques g\u00e8nes \u00e0 un prix beaucoup plus \u00e9lev\u00e9. Cliquez ici pour en savoir plus!<\/a><\/strong><\/td><\/tr><\/tbody><\/table><\/figure>\n\n<h2 class=\"wp-block-heading\" id=\"h-company-overview\"><strong>Pr\u00e9sentation de l&rsquo;entreprise<\/strong><\/h2>\n\n<p>GeneDx est une soci\u00e9t\u00e9 de tests de diagnostic clinique sp\u00e9cialis\u00e9e dans le diagnostic des maladies rares. GeneDx a \u00e9t\u00e9 fond\u00e9e en 2000 dans le cadre de Bio reference Laboratories par deux scientifiques des National Institutes of Health (NIH), les Drs. Sherri Bale et John Compton. L&rsquo;entreprise appartient \u00e0 Okpo Health.<\/p>\n\n<p>GeneDx croit en des tests et des diagnostics responsables pour de meilleurs soins aux patients. L&rsquo;entreprise se concentre sur les tests permettant de diagnostiquer les troubles g\u00e9n\u00e9tiques rares et ultra-rare. La soci\u00e9t\u00e9 essaie de contrecarrer les conseils diagnostiques traditionnels de \u00abQuand vous entendez des battements de sabots, pensez aux chevaux, pas aux z\u00e8bres\u00bb en se concentrant uniquement sur les rares \u00abz\u00e8bres\u00bb.<\/p>\n\n<p>Le premier test de diagnostic de l&rsquo;entreprise en 2007 utilis\u00e9<a href=\"https:\/\/www.nature.com\/scitable\/topicpage\/microarray-based-comparative-genomic-hybridization-acgh-45432\/#\" target=\"_blank\" rel=\"noreferrer noopener\"> hybridation g\u00e9nomique comparative<\/a> pour rechercher des variations de taille allant des duplications ou d\u00e9l\u00e9tions d&rsquo;un seul g\u00e8ne \u00e0 des anomalies chromosomiques enti\u00e8res. <\/p>\n\n<p>En 2008, elle a \u00e9galement commenc\u00e9 \u00e0 utiliser le <a href=\"https:\/\/www.ebi.ac.uk\/training\/online\/course\/ebi-next-generation-sequencing-practical-course\/what-you-will-learn\/what-next-generation-dna-\" target=\"_blank\" rel=\"noreferrer noopener\">s\u00e9quen\u00e7age de nouvelle g\u00e9n\u00e9ration<\/a>, qui donne une bien meilleure r\u00e9solution. Cela permet de trouver des changements (variantes) dans l&rsquo;ADN qui n&rsquo;affectent qu&rsquo;une seule lettre de l&rsquo;alphabet de l&rsquo;ADN.  <\/p>\n\n<p>GeneDx a commenc\u00e9 son s\u00e9quen\u00e7age de nouvelle g\u00e9n\u00e9ration avec des panels de g\u00e8nes cibl\u00e9s pour des maladies rares sp\u00e9cifiques. Ainsi, les m\u00e9decins peuvent d\u00e9sormais v\u00e9rifier si un g\u00e8ne cass\u00e9 particulier est \u00e0 l&rsquo;origine d&rsquo;un trouble.  <\/p>\n\n<p>Plus d&rsquo;options de test sont devenues disponibles au d\u00e9but des ann\u00e9es 2010. En 2012, elle a commenc\u00e9 \u00e0 proposer le s\u00e9quen\u00e7age de l&rsquo;exome entier, qui examine les r\u00e9gions du g\u00e9nome codant pour les prot\u00e9ines. Depuis 2017, GeneDx propose \u00e9galement le s\u00e9quen\u00e7age du g\u00e9nome entier. Le s\u00e9quen\u00e7age de l&rsquo;exome entier et du g\u00e9nome permet au m\u00e9decin d&rsquo;explorer davantage d&rsquo;options en mati\u00e8re de diagnostic des maladies rares.<\/p>\n\n<h2 class=\"wp-block-heading\" id=\"h-review-of-how-genedx-works\"><strong>Examen du fonctionnement de GeneDx<\/strong><\/h2>\n\n<p>GeneDx travaille directement avec les professionnels de la sant\u00e9. Par cons\u00e9quent, un prestataire de soins de sant\u00e9 agr\u00e9\u00e9 doit commander le test ADN au moyen d&rsquo;un formulaire de demande de test, et les r\u00e9sultats lui sont renvoy\u00e9s.  <\/p>\n\n<p>Premi\u00e8rement, un patient devrait rencontrer son fournisseur de soins de sant\u00e9. Si le m\u00e9decin soup\u00e7onne qu&rsquo;un trouble g\u00e9n\u00e9tique sp\u00e9cifique peut \u00eatre \u00e0 l&rsquo;origine des sympt\u00f4mes, le m\u00e9decin ou le conseiller en g\u00e9n\u00e9tique peut demander le test d&rsquo;un g\u00e8ne particulier ou d&rsquo;un ensemble de g\u00e8nes \u00e0 partir du menu des tests GeneDx. Toutefois, si l&rsquo;affection sp\u00e9cifique est ind\u00e9termin\u00e9e, tous les g\u00e8nes peuvent \u00eatre s\u00e9quenc\u00e9s.  <\/p>\n\n<figure class=\"wp-block-image aligncenter is-resized\"><img decoding=\"async\" src=\"https:\/\/lh5.googleusercontent.com\/ZdAPuT8qImxmau8_HeQSsh4kFuJ8X5MrnylETJPi7wDOR8ynQa5uV_aMqteHA2sFYT2Dyqt281Xa9Shv_9Z9CVxdLTrwEg-XGapH30KK6tGaI39AsFGXxjpPeja0DF48LFHq01rc\" alt=\"Tableau contenant des listes avec les tests, leurs codes, leurs noms, le nombre de g&#xE8;nes o&#xF9; se trouve l'affection recherch&#xE9;e et la liste de ces g&#xE8;nes.\" width=\"1028\" height=\"1032\"\/><figcaption>Exemple de menu de test g\u00e9n\u00e9tique GeneDx (de la clinique Mayo)<\/figcaption><\/figure>\n\n<p>Ensuite, le patient doit soumettre un \u00e9chantillon. Des tests diff\u00e9rents ont des exigences diff\u00e9rentes. Mais GeneDx fonctionne avec tout ce dont il peut extraire suffisamment d&rsquo;ADN, y compris le<a href=\"https:\/\/www.genedx.com\/specimen-requirements\/\" target=\"_blank\" rel=\"noreferrer noopener\"> sang, les pr\u00e9l\u00e8vements de joue, les biopsies cutan\u00e9es et m\u00eame l&rsquo;amniocent\u00e8se pour le d\u00e9pistage pr\u00e9natal<\/a>.<\/p>\n\n<p>Enfin, le m\u00e9decin recevra un rapport. Cela peut prendre jusqu&rsquo;\u00e0 16 semaines pour le s\u00e9quen\u00e7age complet du g\u00e9nome. <\/p>\n\n<p>La soci\u00e9t\u00e9 propose \u00e9galement le s\u00e9quen\u00e7age rapide de l&rsquo;exome gr\u00e2ce \u00e0 son produit <em>Xpress<\/em>. Ce test est destin\u00e9 aux patients gravement malades qui pr\u00e9sentent de nombreux sympt\u00f4mes. Les r\u00e9sultats sont disponibles d\u00e8s 7 jours. Il offre notamment un rendement diagnostique allant jusqu&rsquo;\u00e0 58 % pour les nouveau-n\u00e9s et comprend des diagnostics pour les troubles du d\u00e9veloppement neurologique.  <\/p>\n\n<h2 class=\"wp-block-heading\" id=\"h-review-of-a-genedx-sample-report\"><strong>Examen d&rsquo;un \u00e9chantillon de rapport GeneDx<\/strong><\/h2>\n\n<p>Voici un exemple de r\u00e9sultat positif. Au total, le rapport comprend les panels demand\u00e9s, les g\u00e8nes test\u00e9s et les mutations connues responsables de maladies trouv\u00e9es.<\/p>\n\n<figure class=\"wp-block-image aligncenter is-resized\"><img decoding=\"async\" src=\"https:\/\/lh5.googleusercontent.com\/e1lP0REddC_vd-U3RSKHwHdSYbQ56L3s3AH7DOHklNIVQeO9XobLEY7xMybwU_O9BMQ7fAKFGj6ymwrP9EhWwo_Xld7Gg2fuEoI6A3Dp0yFvb8iEQb7NCIhOSm8fbdmr8pRTypz1\" alt=\"Capture d'&#xE9;cran d'un rapport de test GeneDx, avec des annotations en carr&#xE9;s rouges expliquant chaque section du rapport.\" width=\"1139\" height=\"1070\"\/><figcaption>Rapport de test annot\u00e9 de Northwell Health<\/figcaption><\/figure>\n\n<p>Comme vous pouvez le constater, le document contient beaucoup d&rsquo;informations. Il donne un aper\u00e7u des g\u00e8nes \u00e9valu\u00e9s et de leur r\u00e9sultat (positif ou n\u00e9gatif). Les patients obtiennent \u00e9galement des d\u00e9tails int\u00e9ressants, notamment le diagnostic, la signification clinique des mutations trouv\u00e9es et des recommandations.<\/p>\n\n<p>Apr\u00e8s le bloc d&rsquo;informations sur le patient, on trouve la liste des panels command\u00e9s et des g\u00e8nes test\u00e9s. Ici, comme le m\u00e9decin n&rsquo;\u00e9tait pas certain du syndrome correspondant aux sympt\u00f4mes du patient, plusieurs panels ont \u00e9t\u00e9 demand\u00e9s. Cela a conduit au s\u00e9quen\u00e7age de 11 des quelque 20 000 g\u00e8nes diff\u00e9rents. <\/p>\n\n<p>L&rsquo;\u00e9l\u00e9ment le plus important est que cette mutation est \u00ab\u00a0pathog\u00e8ne\u00a0\u00bb &#8211; sur la base des patients que GeneDx a d\u00e9j\u00e0 test\u00e9s, on sait que cette mutation est \u00e0 l&rsquo;origine des sympt\u00f4mes du patient.<\/p>\n\n<p>Le rapport comprend \u00e9galement des recommandations m\u00e9dicales pour le patient et les membres de sa famille. Dans cet exemple, le g\u00e8ne cass\u00e9 identifi\u00e9 est associ\u00e9 \u00e0 des <a href=\"https:\/\/nebula.org\/blog\/fr\/est-insuffisance-cardiaque-congestive-genetique\/\">probl\u00e8mes cardiaques<\/a>, ce qui sugg\u00e8re que le patient devrait faire l&rsquo;objet d&rsquo;un suivi cardiaque. Les m\u00e9decins tiendront \u00e9galement compte du dossier m\u00e9dical du patient lorsqu&rsquo;ils analyseront le rapport.  <\/p>\n\n<p>Enfin, le rapport indique exactement comment le test a \u00e9t\u00e9 effectu\u00e9. <\/p>\n\n<p>Le rapport peut \u00e9galement revenir n\u00e9gatif, ce qui ne signifie pas qu&rsquo;il n&rsquo;y a pas de cause g\u00e9n\u00e9tique \u00e0 ce trouble. <a href=\"https:\/\/www.genedx.com\/test-catalog\/medical-specialty\/xomedx\/\" target=\"_blank\" rel=\"noreferrer noopener\">GeneDX clarifie \u00e9galement ce r\u00e9sultat<\/a> sur son site web.<\/p>\n\n<p>Les r\u00e9sultats peuvent \u00e9galement r\u00e9v\u00e9ler des \u00ab\u00a0variantes de signification incertaine\u00a0\u00bb (VUS), qui sont des variantes test\u00e9es mais qui ne sont pas consid\u00e9r\u00e9es comme un r\u00e9sultat positif &#8211; il n&rsquo;y a pas assez d&rsquo;informations pour affirmer que cette mutation est \u00e0 l&rsquo;origine de la maladie du patient.  <\/p>\n\n<p>N&rsquo;oubliez pas que ce test a des limites. Par exemple, le patient de l&rsquo;exemple ci-dessus peut avoir des mutations non d\u00e9tect\u00e9es ailleurs. Les scientifiques n&rsquo;ont pas r\u00e9pertori\u00e9 toutes les variantes g\u00e9n\u00e9tiques responsables des mutations.<\/p>\n\n<h2 class=\"wp-block-heading\" id=\"h-review-of-genedx-clinician-oversight\"><strong>Examen de la surveillance des cliniciens de GeneDx<\/strong><\/h2>\n\n<p>Dans le cas d&rsquo;un test ADN direct, le consommateur demande le test, soumet son \u00e9chantillon d&rsquo;ADN, paie l&rsquo;analyse et re\u00e7oit les r\u00e9sultats.  <\/p>\n\n<p>Pour GeneDx, le m\u00e9decin soumet la commande et le patient soumet l&rsquo;\u00e9chantillon. Ensuite, le m\u00e9decin recevra les r\u00e9sultats.  <\/p>\n\n<p>Seul un m\u00e9decin peut prescrire un test GeneDx &#8211; soit un m\u00e9decin, soit un DO, soit, dans certains \u00c9tats, un conseiller en g\u00e9n\u00e9tique. Les tests ne peuvent \u00eatre demand\u00e9s que dans le cadre de directives m\u00e9dicales \u00e9tablies, en tant qu&rsquo;outil de diagnostic.<\/p>\n\n<p>Les r\u00e9sultats sont uniquement renvoy\u00e9s au m\u00e9decin. GeneDx emploie des conseillers en g\u00e9n\u00e9tique, mais ce sont des conseillers en g\u00e9n\u00e9tique de laboratoire GeneDx qui ne travaillent pas directement avec le patient. Leur r\u00f4le consiste plut\u00f4t \u00e0 travailler sur les cas et \u00e9ventuellement \u00e0 former un clinicien ordonnateur.  <\/p>\n\n<p>Les services de conseil g\u00e9n\u00e9tique sont recommand\u00e9s mais non fournis par GeneDx. Vous pouvez acc\u00e9der \u00e0 des conseillers en g\u00e9n\u00e9tique par le biais d&rsquo;entreprises telles que <a href=\"https:\/\/nebula.org\/blog\/genome-medical-review\/\">Genome Medical<\/a>.  <\/p>\n\n<h2 class=\"wp-block-heading\" id=\"h-review-of-genedx-costs\"><strong>Examen des co\u00fbts de GeneDx<\/strong><\/h2>\n\n<p>Le test \u00e9tant une proc\u00e9dure de diagnostic m\u00e9dical, le prix varie en fonction des sp\u00e9cificit\u00e9s du test et de l&rsquo;assureur.<\/p>\n\n<p>L&rsquo;entreprise offre une aide financi\u00e8re en fonction du revenu et de la taille du m\u00e9nage, y compris un prix de compassion et des plans de paiement. Les d\u00e9tails sur les prix ne sont pas disponibles publiquement.<\/p>\n\n<h2 class=\"wp-block-heading\" id=\"h-review-of-genedx-privacy\"><strong>Examen de la confidentialit\u00e9 de GeneDx<\/strong><\/h2>\n\n<p>En tant que soci\u00e9t\u00e9 de diagnostic m\u00e9dical, GeneDx doit se conformer au R\u00e8glement g\u00e9n\u00e9ral sur la protection des donn\u00e9es (RGPD) de l&rsquo;Union europ\u00e9enne, \u00e0 la loi am\u00e9ricaine sur la portabilit\u00e9 et la responsabilit\u00e9 en mati\u00e8re d&rsquo;assurance maladie (HIPAA) et \u00e0 la loi sur les technologies de l&rsquo;information en mati\u00e8re de sant\u00e9 (HITECH).<\/p>\n\n<p>GeneDx rapporte les variantes qu&rsquo;il trouve \u00e0 <a href=\"https:\/\/www.ncbi.nlm.nih.gov\/clinvar\/intro\/\" target=\"_blank\" rel=\"noreferrer noopener\">ClinVar<\/a>, une base de donn\u00e9es accessible au public. Les <a href=\"https:\/\/www.ncbi.nlm.nih.gov\/clinvar\/RCV000239819\/\" target=\"_blank\" rel=\"noreferrer noopener\">donn\u00e9es<\/a> ne peuvent \u00eatre associ\u00e9es \u00e0 un individu, mais elles aident d&rsquo;autres g\u00e9n\u00e9ticiens \u00e0 \u00e9tablir un lien entre les modifications de l&rsquo;ADN et leurs cons\u00e9quences m\u00e9dicales chez l&rsquo;homme.  <\/p>\n\n<p>Dans son avis sur les pratiques en mati\u00e8re de confidentialit\u00e9 (NOPP), la soci\u00e9t\u00e9 affirme qu&rsquo;elle ne r\u00e9v\u00e9lera pas vos informations de sant\u00e9 prot\u00e9g\u00e9es (PHI). Toutefois, elle informera certaines personnes dans le cas de traitements, de prestations, de services, d&rsquo;infirmi\u00e8res, de m\u00e9decins et de prestataires de soins de sant\u00e9 impliqu\u00e9s dans vos soins. Dans d&rsquo;autres cas, il s&rsquo;agit de la facturation et de la collecte des paiements de soins de sant\u00e9 et d&rsquo;autres cas applicables lorsque la loi l&rsquo;exige.<\/p>\n\n<h2 class=\"wp-block-heading\" id=\"h-genedx-in-the-news\"><strong>GeneDx dans la presse<\/strong><\/h2>\n\n<p>Depuis sa cr\u00e9ation en 2000, GeneDx s&rsquo;est efforc\u00e9 de rester au courant des progr\u00e8s de la g\u00e9n\u00e9tique m\u00e9dicale et des <a href=\"https:\/\/www.prnewswire.com\/news-releases\/debbies-dream-foundation-curing-stomach-cancer-hosts-virtual-stomach-cancer-educational-symposium-301472372.html\" target=\"_blank\" rel=\"noreferrer noopener\">expositions connexes<\/a>. Cela en a fait un acteur important sur le <a href=\"https:\/\/www.digitaljournal.com\/pr\/global-rare-disease-genetic-testing-market-projected-to-gain-significant-value-by-2030\" target=\"_blank\" rel=\"noreferrer noopener\">march\u00e9 mondial des tests g\u00e9n\u00e9tiques pour les maladies rares<\/a>.  <\/p>\n\n<p>En septembre 2021, la soci\u00e9t\u00e9 a annonc\u00e9 le <a href=\"https:\/\/www.prnewswire.com\/news-releases\/genedx-announces-the-sequencing-of-more-than-300-000-clinical-patient-exomes-301381900.html\" target=\"_blank\" rel=\"noreferrer noopener\">s\u00e9quen\u00e7age de plus de 300 000 exomes de patients cliniques<\/a>. Il s&rsquo;agit du plus grand ensemble de donn\u00e9es cliniques de ce type au monde.  <\/p>\n\n<p>La m\u00eame ann\u00e9e, en octobre, GeneDx <a href=\"https:\/\/www.globenewswire.com\/news-release\/2021\/10\/12\/2312509\/0\/en\/Krystal-Biotech-and-GeneDx-Announce-Collaboration-to-Provide-No-charge-Genetic-Testing-for-Patients-with-Suspected-Dystrophic-Epidermolysis-Bullosa-DEB.html\" target=\"_blank\" rel=\"noreferrer noopener\">s&rsquo;est associ\u00e9 \u00e0 Krystal Biotech<\/a> pour proposer un produit appel\u00e9 Krystal Decode DEB. Ce programme a pour objectif d&rsquo;aider les patients suspect\u00e9s d&rsquo;\u00e9pidermolyse bulleuse dystrophique (une maladie g\u00e9n\u00e9tique rare de la peau) \u00e0 b\u00e9n\u00e9ficier d&rsquo;un diagnostic pr\u00e9coce et de soins optimaux.  <\/p>\n\n<p>En outre, la soci\u00e9t\u00e9 de veille sanitaire Sema4 <a href=\"https:\/\/www.opko.com\/news-media\/press-releases\/detail\/465\/sema4-announces-the-completion-of-the-genedx-acquisition\" target=\"_blank\" rel=\"noreferrer noopener\">a acquis GeneDx pour environ 623 millions de dollars<\/a> en mai 2022. Cet accord renforcera l&rsquo;application de l&rsquo;intelligence artificielle de Sema4 aux soins de sant\u00e9.<\/p>\n\n<h2 class=\"wp-block-heading\" id=\"h-other-genedx-reviews\"><strong>Autres avis sur GeneDx<\/strong><\/h2>\n\n<p>Les avis sur GeneDx sur <a href=\"https:\/\/www.yelp.com\/biz\/genedx-gaithersburg\" target=\"_blank\" rel=\"noreferrer noopener\">Yelp<\/a> ont une note moyenne de 1,5 \u00e9toile. Les avis se plaignent de co\u00fbts impr\u00e9vus , retards dans les tests , tactiques de vente \u00e0 haute pression , et changements de r\u00e9sultats . <\/p>\n\n<p>Les <a href=\"https:\/\/www.google.com\/maps\/place\/GeneDx\/@39.1428258,-77.2100258,17z\/data=!4m7!3m6!1s0x89b62d3b2c20f3c5:0xb36881b8507f8fb5!8m2!3d39.1428258!4d-77.2078371!9m1!1b1\" target=\"_blank\" rel=\"noreferrer noopener\">avis Google sur<\/a> GeneDx sont en moyenne de 1,9\/5, avec des plaintes similaires concernant des probl\u00e8mes d&rsquo;assurance et des plaintes d&rsquo;anciens employ\u00e9s.<\/p>\n\n<p>Le <a href=\"https:\/\/www.bbb.org\/us\/md\/gaithersburg\/profile\/diagnostic-testing\/genedx-inc-0241-235999900\/complaints\" target=\"_blank\" rel=\"noreferrer noopener\">Better Business Bureau<\/a> attribue \u00e0 GeneDx la note A+, mais notez que cette note ne tient pas compte des avis des clients.  <\/p>\n\n<p>Certains<a href=\"https:\/\/www.glassdoor.com\/Reviews\/GeneDx-Reviews-E382258.htm\" target=\"_blank\" rel=\"noreferrer noopener\"> Commentaires<\/a> concernant les carri\u00e8res de GeneDx sugg\u00e8rent qu&rsquo;il y avait auparavant un environnement de travail toxique dans l&rsquo;entreprise. C&rsquo;est peut-\u00eatre un bon endroit pour travailler fra\u00eechement sorti de l&rsquo;universit\u00e9, mais moins appropri\u00e9 pour une carri\u00e8re \u00e0 long terme.<\/p>\n\n<h2 class=\"wp-block-heading\" id=\"h-nebula-genomics\"><strong>G\u00e9nomique des n\u00e9buleuses<\/strong><\/h2>\n\n<p>Nebula Genomics offre un s\u00e9quen\u00e7age de l&rsquo;ADN \u00e0 plus haut niveau de couverture, s&rsquo;efforce d&rsquo;\u00e9duquer et de responsabiliser l&rsquo;utilisateur, et co\u00fbte moins cher que les tests ADN diagnostiques.<\/p>\n\n<h3 class=\"wp-block-heading\" id=\"h-30x-whole-genome-sequencing\">S\u00e9quen\u00e7age du g\u00e9nome entier 30x<\/h3>\n\n<p>Le s\u00e9quen\u00e7age de l&rsquo;exome entier couvre environ 2% du g\u00e9nome. GeneDx effectue les tests de mani\u00e8re \u00e0 ce qu&rsquo;au moins 95 % de l&rsquo;ADN soit s\u00e9quenc\u00e9 au moins dix fois (ce que l&rsquo;on appelle la couverture 10x). Au moins 98% est s\u00e9quenc\u00e9 au moins une fois.  <\/p>\n\n<p>Nebula Genomics va plus loin : non seulement l&rsquo;ensemble du g\u00e9nome est s\u00e9quenc\u00e9, mais chaque morceau est \u00e9galement s\u00e9quenc\u00e9 30 fois en moyenne. Une couverture de s\u00e9quen\u00e7age plus \u00e9lev\u00e9e offre une meilleure pr\u00e9cision pour trouver des variantes d&rsquo;ADN.<\/p>\n\n<h3 class=\"wp-block-heading\" id=\"h-nebula-empowers-the-user-to-learn-about-their-own-dna\">Nebula permet \u00e0 l&rsquo;utilisateur de d\u00e9couvrir son propre ADN<\/h3>\n\n<p>Nous voulons que les gens apprennent \u00e0 conna\u00eetre leur sant\u00e9, leur personnalit\u00e9 et leur ascendance. <a href=\"https:\/\/nebula.org\/blog\/fr\/rendre-la-science-accessible-a-tous\/\">Nebula s&rsquo;engage \u00e0 expliquer la science de pointe de mani\u00e8re simple et pr\u00e9cise<\/a>. Nebula estime que les individus devraient avoir la libert\u00e9 de prendre en charge leurs informations g\u00e9nomiques. Cela inclut l&rsquo;utilisation de la <a href=\"https:\/\/nebula.org\/blog\/fr\/recherche-genetique-deblocage-bibliotheque-nebuleuse\/\">biblioth\u00e8que de recherche Nebula<\/a> pour parcourir les \u00e9tudes de recherche conserv\u00e9es.<\/p>\n\n<p>Nebula permet \u00e9galement aux utilisateurs d&rsquo;acc\u00e9der \u00e0 toutes leurs donn\u00e9es. Les utilisateurs peuvent t\u00e9l\u00e9charger leurs donn\u00e9es g\u00e9nomiques brutes et les consulter eux-m\u00eames. Nebula fournit m\u00eame i des informations sur la fa\u00e7on de commencer et des explications sur ce que tout cela signifie .<\/p>\n\n<figure class=\"wp-block-table is-style-regular\"><table><tbody><tr><td><br\/><\/td><td>GeneDx<\/td><td><br\/>23andMe<\/td><td>AncestryDNA<\/td><td>G\u00e9nomique des n\u00e9buleuses<\/td><\/tr><tr><td>M\u00e9thode de test ADN<\/td><td>Prochaine g\u00e9n\u00e9ration (g\u00e8ne unique, g\u00e8nes multiples, tous les g\u00e8nes ou g\u00e9nome entier) ou hybridation <\/td><td>G\u00e9notypage bas\u00e9 sur des puces \u00e0 ADN<\/td><td>G\u00e9notypage bas\u00e9 sur des puces \u00e0 ADN<\/td><td>La prochaine g\u00e9n\u00e9ration<a href=\"https:\/\/nebula.org\/blog\/fr\/30x-wgs\/\"> (S\u00e9quen\u00e7age du g\u00e9nome entier avec une couverture 30x)<\/a><\/td><\/tr><tr><td>Capable de t\u00e9l\u00e9charger des donn\u00e9es ADN brutes<\/td><td>Non<\/td><td>Non<\/td><td>Non<\/td><td>Oui (23andMe et Ancestry)<\/td><\/tr><tr><td>Acc\u00e8s aux donn\u00e9es t\u00e9l\u00e9chargeables<\/td><td>Non<\/td><td>Oui (fichier au format 23andMe)<\/td><td>Oui (fichier au format Ancestry)<\/td><td>Oui (fichiers FASTQ, BAM et VCF)<\/td><\/tr><tr><td>Ordres des m\u00e9decins n\u00e9cessaires  <\/td><td>Oui<\/td><td>Non<\/td><td>Non<\/td><td>Non<\/td><\/tr><tr><td>Explications informatives et p\u00e9dagogiques<\/td><td>Non<\/td><td>Oui <\/td><td>Oui<\/td><td>Oui<\/td><\/tr><tr><td>Outils de recherche de rapports simplifi\u00e9s<\/td><td>Non<\/td><td>Oui<\/td><td>Oui<\/td><td>Oui (<a href=\"https:\/\/nebula.org\/blog\/fr\/category\/rapports\/\"> apprendre encore plus<\/a> )<\/td><\/tr><tr><td>Co\u00fbt<\/td><td>Variable et souvent impr\u00e9visible<\/td><td>99 $ ou 199 $.<\/td><td>99 $ ou 119 $<\/td><td><a href=\"https:\/\/nebula.org\/whole-genome-sequencing\/\">0 $, 99 $, 299 $<\/a><\/td><\/tr><\/tbody><\/table><\/figure>\n\n<p>D&rsquo;autres soci\u00e9t\u00e9s sp\u00e9cialis\u00e9es dans le diagnostic des maladies rares sont <a href=\"https:\/\/nebula.org\/blog\/centogene-review\/\">CENTOGENE<\/a> et <a href=\"https:\/\/nebula.org\/blog\/stripe2be-review\/\" target=\"_blank\" rel=\"noreferrer noopener\">Stripe2be<\/a>.  <\/p>\n\n<p>Les entreprises qui utilisent la g\u00e9nomique pour d\u00e9velopper de nouvelles th\u00e9rapies peuvent \u00e9galement vous int\u00e9resser : <a href=\"https:\/\/nebula.org\/blog\/deep-genomics-review\/\" target=\"_blank\" rel=\"noreferrer noopener\">Deep Genomics<\/a> (troubles du SNC et du m\u00e9tabolisme) et <a href=\"https:\/\/nebula.org\/blog\/verge-genomics-review\/\" target=\"_blank\" rel=\"noreferrer noopener\">Verge Genomics<\/a> (troubles neurog\u00e9n\u00e9ratifs).<\/p>\n\n<p>Si vous \u00eates int\u00e9ress\u00e9 par les tests de diagnostic, vous aimerez peut-\u00eatre ces autres articles.<\/p>\n\n<p>Diagnostics et risques de maladies\u00a0:<\/p>\n\n<ul class=\"wp-block-list\"><li><a href=\"https:\/\/nebula.org\/blog\/fr\/revue-ambry-genetics\/\">G\u00e9n\u00e9tique Ambry<\/a> (risques de divers types de maladies)<\/li><li><a href=\"https:\/\/nebula.org\/blog\/fr\/examen-de-la-genomique-des-couleurs\/\">Couleur<\/a> (risques de cancer, formes g\u00e9n\u00e9tiques de maladies cardiaques et r\u00e9ponses aux m\u00e9dicaments)<\/li><li><a href=\"https:\/\/nebula.org\/blog\/fulgent-genetics-review\/\">Fulgent Genetics<\/a> (soci\u00e9t\u00e9 de diagnostic complet)<\/li><li><a href=\"https:\/\/nebula.org\/blog\/fr\/oral-dna-labs-examen\/\">Oral DNA Labs<\/a> (outil pour la sant\u00e9 bucco-dentaire)<\/li><li><a href=\"https:\/\/nebula.org\/blog\/map-my-gene-review\/\">Map My Gene<\/a> (talents inn\u00e9s pour les enfants et les risques de maladie)<\/li><li><a href=\"https:\/\/nebula.org\/blog\/parsley-health\/\">Sant\u00e9 du persil<\/a> (m\u00e9decine holistique et plans de sant\u00e9)<\/li><li><a href=\"https:\/\/nebula.org\/blog\/fr\/examen-des-voies-genomiques\/\">G\u00e9nomique des voies<\/a> (Des tests ADN pour divers aspects de la sant\u00e9 peuvent \u00eatre utilis\u00e9s en consultation avec des prestataires m\u00e9dicaux)<\/li><\/ul>\n\n<p>Inclut le statut de transporteur\u00a0:<\/p>\n\n<ul class=\"wp-block-list\"><li><a href=\"https:\/\/nebula.org\/blog\/fr\/examen-genetique-integre\/\">G\u00e9n\u00e9tique int\u00e9gr\u00e9e<\/a> (tests pr\u00e9 et post grossesse)<\/li><li><a href=\"https:\/\/nebula.org\/blog\/fr\/invitae-examen\/\">Invitae<\/a> (diagnostic, sant\u00e9 proactive et sant\u00e9 reproductive)<\/li><li><a href=\"https:\/\/nebula.org\/blog\/fr\/myriade-revue-genetique\/\">Myriad Genetics<\/a> (diagnostics, tests de reproduction et tests de m\u00e9decine de pr\u00e9cision)<\/li><li><a href=\"https:\/\/nebula.org\/blog\/picture-genetics-review\/\">Picture Genetics<\/a> (test \u00e0 domicile effectu\u00e9 dans un laboratoire de diagnostic)<\/li><li><a href=\"https:\/\/nebula.org\/blog\/sema4-review\/\">Sema4<\/a> (oncologie, sant\u00e9 des femmes, d\u00e9pistage des porteurs et cancer h\u00e9r\u00e9ditaire)<\/li><li><a href=\"https:\/\/nebula.org\/blog\/fr\/revue-de-genetique-veritas\/\">Veritas Genetics<\/a> (risques de maladie et d\u00e9pistage des porteurs)<\/li><\/ul>\n\n<p>Sant\u00e9 mentale:<\/p>\n\n<ul class=\"wp-block-list\" id=\"block-77fa48a3-93c6-4e4a-b5f3-7a09486fc076\"><li><a href=\"https:\/\/nebula.org\/blog\/fr\/revue-genesight\/\">GeneSight<\/a> (test g\u00e9nomique pour les psychotropes)<\/li><li><a href=\"https:\/\/nebula.org\/blog\/fr\/examen-genomique\/\">Genomind<\/a> (tests pharmacog\u00e9nomiques pour le traitement de la sant\u00e9 mentale)<\/li><\/ul>\n\n<p>La g\u00e9n\u00e9tique des tumeurs :<\/p>\n\n<ul class=\"wp-block-list\"><li><a href=\"https:\/\/nebula.org\/blog\/decipher-biosciences-review\/\">Decipher Biosciences<\/a> (g\u00e9n\u00e9tique tumorale pour les cancers urologiques)<\/li><li><a href=\"https:\/\/nebula.org\/blog\/foundation-medicine-review\/\">Foundation Medicine<\/a> (analyse g\u00e9n\u00e9tique sur les tumeurs solides)<\/li><li><a href=\"https:\/\/nebula.org\/blog\/natera-review\/\">Natera<\/a> (ADN circulant pour le cancer h\u00e9r\u00e9ditaire et d&rsquo;autres diagnostics)<\/li><li><a href=\"https:\/\/nebula.org\/blog\/tempus-labs-review\/\">Tempus<\/a> (oncologie, sant\u00e9 mentale et traitement des maladies infectieuses)<\/li><\/ul>\n\n<p>De plus, il existe d&rsquo;autres tests ADN qui permettent le s\u00e9quen\u00e7age de l&rsquo;exome entier :<\/p>\n\n<ul class=\"wp-block-list\"><li><a href=\"https:\/\/nebula.org\/blog\/24genetics-review\/\">24G\u00e9n\u00e9tique<\/a><\/li><li><a href=\"https:\/\/nebula.org\/blog\/fr\/revue-circledna\/\">CircleDNA<\/a><\/li><li><a href=\"https:\/\/nebula.org\/blog\/fr\/examen-dante-labs\/\">Laboratoires Dante<\/a><\/li><li><a href=\"https:\/\/nebula.org\/blog\/fr\/examen-dnafit\/\">DNAFit<\/a> (avec CircleDNA)<\/li><li><a href=\"https:\/\/nebula.org\/blog\/fr\/helix-dna-revue\/\">Helix DNA <\/a>(test ADN et un co\u00fbt suppl\u00e9mentaire pour les applications)<\/li><li><a href=\"https:\/\/nebula.org\/blog\/fr\/tellmegen-examen\/\">tellmeGen<\/a><\/li><\/ul>\n\n<p>En savoir plus sur<a href=\"https:\/\/nebula.org\/blog\/fr\/sequencage-complet-de-lexome\/\"> s\u00e9quen\u00e7age complet de l&rsquo;exome<\/a> !<\/p>\n\n<p>Avez-vous aim\u00e9 l&rsquo;examen de GeneDx? Tu peux trouver<a href=\"https:\/\/nebula.org\/blog\/fr\/category\/reviews-fr\/\"> plus d&rsquo;avis<\/a> sur notre blog et consultez notre<a href=\"https:\/\/nebula.org\/blog\/fr\/meilleurs-kits-de-test-adn\/\"> guide complet du meilleur kit de test ADN et autres tests \u00e0 domicile<\/a> .<\/p>\n","protected":false},"excerpt":{"rendered":"<p>7 faits tir\u00e9s de notre examen de GeneDx Emplacement: Gaithersburg, Maryland Produits : Grande vari\u00e9t\u00e9 de tests g\u00e9nomiques cliniques, g\u00e9n\u00e9tique m\u00e9dicale sur les troubles g\u00e9n\u00e9tiques rares. Rapports : Rapports de sant\u00e9 d\u00e9taill\u00e9s pour des conditions g\u00e9n\u00e9tiques sp\u00e9cifiques Livraison du r\u00e9sultat &hellip;<\/p>\n<p class=\"read-more\"> <a class=\"ast-button\" href=\"https:\/\/nebula.org\/blog\/fr\/revue-genedx\/\"> <span class=\"screen-reader-text\">Examen de GeneDx &#8211; Transformer les donn\u00e9es en diagnostic de maladies rares ?<\/span> Lire la suite \u00bb<\/a><\/p>\n","protected":false},"author":16,"featured_media":35975,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"om_disable_all_campaigns":false,"site-sidebar-layout":"default","site-content-layout":"default","ast-global-header-display":"","ast-banner-title-visibility":"","ast-main-header-display":"","ast-hfb-above-header-display":"","ast-hfb-below-header-display":"","ast-hfb-mobile-header-display":"","site-post-title":"","ast-breadcrumbs-content":"","ast-featured-img":"","footer-sml-layout":"","theme-transparent-header-meta":"default","adv-header-id-meta":"","stick-header-meta":"default","header-above-stick-meta":"","header-main-stick-meta":"","header-below-stick-meta":"","_FSMCFIC_featured_image_caption":"","_FSMCFIC_featured_image_nocaption":"","_FSMCFIC_featured_image_hide":"","footnotes":""},"categories":[4973],"tags":[],"class_list":["post-9377","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-reviews-fr"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v20.13 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Examen de GeneDx - 7 faits \u00e0 savoir [SEPTEMBER 2022]<\/title>\n<meta name=\"description\" content=\"GeneDx est une soci\u00e9t\u00e9 de tests g\u00e9n\u00e9tiques cliniques sp\u00e9cialis\u00e9e dans le diagnostic des maladies rares. Apprenez-en plus dans notre revue GeneDx!\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/nebula.org\/blog\/fr\/revue-genedx\/\" \/>\n<meta property=\"og:locale\" content=\"fr_FR\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Examen de GeneDx - 7 faits \u00e0 savoir [SEPTEMBER 2022]\" \/>\n<meta property=\"og:description\" content=\"GeneDx est une soci\u00e9t\u00e9 de tests g\u00e9n\u00e9tiques cliniques sp\u00e9cialis\u00e9e dans le diagnostic des maladies rares. Apprenez-en plus dans notre revue GeneDx!\" \/>\n<meta property=\"og:url\" content=\"https:\/\/nebula.org\/blog\/fr\/revue-genedx\/\" \/>\n<meta property=\"og:site_name\" content=\"Nebula Genomics Blog\" \/>\n<meta property=\"article:publisher\" content=\"https:\/\/facebook.com\/nebulagenomics\" \/>\n<meta property=\"article:published_time\" content=\"2021-01-06T03:43:35+00:00\" \/>\n<meta property=\"article:modified_time\" content=\"2022-11-21T13:22:27+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/nebula.org\/blog\/wp-content\/uploads\/2022\/09\/blood-test.jpg\" \/>\n\t<meta property=\"og:image:width\" content=\"1600\" \/>\n\t<meta property=\"og:image:height\" content=\"1200\" \/>\n\t<meta property=\"og:image:type\" content=\"image\/jpeg\" \/>\n<meta name=\"author\" content=\"Nikki Teran, B.S.\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:creator\" content=\"@nebulagenomics\" \/>\n<meta name=\"twitter:site\" content=\"@nebulagenomics\" \/>\n<meta name=\"twitter:label1\" content=\"\u00c9crit par\" \/>\n\t<meta name=\"twitter:data1\" content=\"Nikki Teran, B.S.\" \/>\n\t<meta name=\"twitter:label2\" content=\"Dur\u00e9e de lecture estim\u00e9e\" \/>\n\t<meta name=\"twitter:data2\" content=\"15 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\/\/nebula.org\/blog\/fr\/revue-genedx\/#article\",\"isPartOf\":{\"@id\":\"https:\/\/nebula.org\/blog\/fr\/revue-genedx\/\"},\"author\":{\"name\":\"Nikki Teran, B.S.\",\"@id\":\"https:\/\/nebula.org\/blog\/fr\/#\/schema\/person\/3b2737c7f39b77815cfdbc95d95bc0c8\"},\"headline\":\"Examen de GeneDx &#8211; Transformer les donn\u00e9es en diagnostic de maladies rares ?\",\"datePublished\":\"2021-01-06T03:43:35+00:00\",\"dateModified\":\"2022-11-21T13:22:27+00:00\",\"mainEntityOfPage\":{\"@id\":\"https:\/\/nebula.org\/blog\/fr\/revue-genedx\/\"},\"wordCount\":3236,\"publisher\":{\"@id\":\"https:\/\/nebula.org\/blog\/fr\/#organization\"},\"articleSection\":[\"Reviews\"],\"inLanguage\":\"fr-FR\",\"accessibilityFeature\":[\"tableOfContents\"]},{\"@type\":\"WebPage\",\"@id\":\"https:\/\/nebula.org\/blog\/fr\/revue-genedx\/\",\"url\":\"https:\/\/nebula.org\/blog\/fr\/revue-genedx\/\",\"name\":\"Examen de GeneDx - 7 faits \u00e0 savoir [SEPTEMBER 2022]\",\"isPartOf\":{\"@id\":\"https:\/\/nebula.org\/blog\/fr\/#website\"},\"datePublished\":\"2021-01-06T03:43:35+00:00\",\"dateModified\":\"2022-11-21T13:22:27+00:00\",\"description\":\"GeneDx est une soci\u00e9t\u00e9 de tests g\u00e9n\u00e9tiques cliniques sp\u00e9cialis\u00e9e dans le diagnostic des maladies rares. Apprenez-en plus dans notre revue GeneDx!\",\"breadcrumb\":{\"@id\":\"https:\/\/nebula.org\/blog\/fr\/revue-genedx\/#breadcrumb\"},\"inLanguage\":\"fr-FR\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\/\/nebula.org\/blog\/fr\/revue-genedx\/\"]}]},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\/\/nebula.org\/blog\/fr\/revue-genedx\/#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"Home\",\"item\":\"https:\/\/nebula.org\/blog\/fr\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"Examen de GeneDx &#8211; Transformer les donn\u00e9es en diagnostic de maladies rares ?\"}]},{\"@type\":\"WebSite\",\"@id\":\"https:\/\/nebula.org\/blog\/fr\/#website\",\"url\":\"https:\/\/nebula.org\/blog\/fr\/\",\"name\":\"Nebula Genomics Blog\",\"description\":\"\",\"publisher\":{\"@id\":\"https:\/\/nebula.org\/blog\/fr\/#organization\"},\"potentialAction\":[{\"@type\":\"SearchAction\",\"target\":{\"@type\":\"EntryPoint\",\"urlTemplate\":\"https:\/\/nebula.org\/blog\/fr\/?s={search_term_string}\"},\"query-input\":\"required name=search_term_string\"}],\"inLanguage\":\"fr-FR\"},{\"@type\":\"Organization\",\"@id\":\"https:\/\/nebula.org\/blog\/fr\/#organization\",\"name\":\"Nebula Genomics\",\"url\":\"https:\/\/nebula.org\/blog\/fr\/\",\"logo\":{\"@type\":\"ImageObject\",\"inLanguage\":\"fr-FR\",\"@id\":\"https:\/\/nebula.org\/blog\/fr\/#\/schema\/logo\/image\/\",\"url\":\"\",\"contentUrl\":\"\",\"caption\":\"Nebula Genomics\"},\"image\":{\"@id\":\"https:\/\/nebula.org\/blog\/fr\/#\/schema\/logo\/image\/\"},\"sameAs\":[\"https:\/\/facebook.com\/nebulagenomics\",\"https:\/\/twitter.com\/nebulagenomics\",\"https:\/\/www.instagram.com\/nebulagenomics\/\",\"https:\/\/www.linkedin.com\/company\/nebula-genomics\/\",\"https:\/\/en.wikipedia.org\/wiki\/Nebula_Genomics\"]},{\"@type\":\"Person\",\"@id\":\"https:\/\/nebula.org\/blog\/fr\/#\/schema\/person\/3b2737c7f39b77815cfdbc95d95bc0c8\",\"name\":\"Nikki Teran, B.S.\",\"image\":{\"@type\":\"ImageObject\",\"inLanguage\":\"fr-FR\",\"@id\":\"https:\/\/nebula.org\/blog\/fr\/#\/schema\/person\/image\/\",\"url\":\"https:\/\/nebula.org\/blog\/wp-content\/uploads\/2021\/01\/1535048906589-150x150.jpeg\",\"contentUrl\":\"https:\/\/nebula.org\/blog\/wp-content\/uploads\/2021\/01\/1535048906589-150x150.jpeg\",\"caption\":\"Nikki Teran, B.S.\"},\"description\":\"Nikki Teran earned a B.S. in Molecular Biophysics and Biochemistry from Yale University. She is currently a Ph.D. Candidate in Genetics at Stanford University.\u00a0She has experience in technical writing at both Nebula Genomics and Ancestry DNA and scientific research experience as a Computation Biology intern at twoXar Pharmaceuticals.\u00a0Nikki is a member of the Montgomery lab at Stanford University. You can read more about Nikki's experience on LinkedIn and ORCID.\",\"url\":\"https:\/\/nebula.org\/blog\/fr\/author\/nikki-teran\/\"}]}<\/script>\n<!-- \/ Yoast SEO plugin. -->","yoast_head_json":{"title":"Examen de GeneDx - 7 faits \u00e0 savoir [SEPTEMBER 2022]","description":"GeneDx est une soci\u00e9t\u00e9 de tests g\u00e9n\u00e9tiques cliniques sp\u00e9cialis\u00e9e dans le diagnostic des maladies rares. Apprenez-en plus dans notre revue GeneDx!","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/nebula.org\/blog\/fr\/revue-genedx\/","og_locale":"fr_FR","og_type":"article","og_title":"Examen de GeneDx - 7 faits \u00e0 savoir [SEPTEMBER 2022]","og_description":"GeneDx est une soci\u00e9t\u00e9 de tests g\u00e9n\u00e9tiques cliniques sp\u00e9cialis\u00e9e dans le diagnostic des maladies rares. Apprenez-en plus dans notre revue GeneDx!","og_url":"https:\/\/nebula.org\/blog\/fr\/revue-genedx\/","og_site_name":"Nebula Genomics Blog","article_publisher":"https:\/\/facebook.com\/nebulagenomics","article_published_time":"2021-01-06T03:43:35+00:00","article_modified_time":"2022-11-21T13:22:27+00:00","og_image":[{"width":1600,"height":1200,"url":"https:\/\/nebula.org\/blog\/wp-content\/uploads\/2022\/09\/blood-test.jpg","type":"image\/jpeg"}],"author":"Nikki Teran, B.S.","twitter_card":"summary_large_image","twitter_creator":"@nebulagenomics","twitter_site":"@nebulagenomics","twitter_misc":{"\u00c9crit par":"Nikki Teran, B.S.","Dur\u00e9e de lecture estim\u00e9e":"15 minutes"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"Article","@id":"https:\/\/nebula.org\/blog\/fr\/revue-genedx\/#article","isPartOf":{"@id":"https:\/\/nebula.org\/blog\/fr\/revue-genedx\/"},"author":{"name":"Nikki Teran, B.S.","@id":"https:\/\/nebula.org\/blog\/fr\/#\/schema\/person\/3b2737c7f39b77815cfdbc95d95bc0c8"},"headline":"Examen de GeneDx &#8211; Transformer les donn\u00e9es en diagnostic de maladies rares ?","datePublished":"2021-01-06T03:43:35+00:00","dateModified":"2022-11-21T13:22:27+00:00","mainEntityOfPage":{"@id":"https:\/\/nebula.org\/blog\/fr\/revue-genedx\/"},"wordCount":3236,"publisher":{"@id":"https:\/\/nebula.org\/blog\/fr\/#organization"},"articleSection":["Reviews"],"inLanguage":"fr-FR","accessibilityFeature":["tableOfContents"]},{"@type":"WebPage","@id":"https:\/\/nebula.org\/blog\/fr\/revue-genedx\/","url":"https:\/\/nebula.org\/blog\/fr\/revue-genedx\/","name":"Examen de GeneDx - 7 faits \u00e0 savoir [SEPTEMBER 2022]","isPartOf":{"@id":"https:\/\/nebula.org\/blog\/fr\/#website"},"datePublished":"2021-01-06T03:43:35+00:00","dateModified":"2022-11-21T13:22:27+00:00","description":"GeneDx est une soci\u00e9t\u00e9 de tests g\u00e9n\u00e9tiques cliniques sp\u00e9cialis\u00e9e dans le diagnostic des maladies rares. Apprenez-en plus dans notre revue GeneDx!","breadcrumb":{"@id":"https:\/\/nebula.org\/blog\/fr\/revue-genedx\/#breadcrumb"},"inLanguage":"fr-FR","potentialAction":[{"@type":"ReadAction","target":["https:\/\/nebula.org\/blog\/fr\/revue-genedx\/"]}]},{"@type":"BreadcrumbList","@id":"https:\/\/nebula.org\/blog\/fr\/revue-genedx\/#breadcrumb","itemListElement":[{"@type":"ListItem","position":1,"name":"Home","item":"https:\/\/nebula.org\/blog\/fr\/"},{"@type":"ListItem","position":2,"name":"Examen de GeneDx &#8211; Transformer les donn\u00e9es en diagnostic de maladies rares ?"}]},{"@type":"WebSite","@id":"https:\/\/nebula.org\/blog\/fr\/#website","url":"https:\/\/nebula.org\/blog\/fr\/","name":"Nebula Genomics Blog","description":"","publisher":{"@id":"https:\/\/nebula.org\/blog\/fr\/#organization"},"potentialAction":[{"@type":"SearchAction","target":{"@type":"EntryPoint","urlTemplate":"https:\/\/nebula.org\/blog\/fr\/?s={search_term_string}"},"query-input":"required name=search_term_string"}],"inLanguage":"fr-FR"},{"@type":"Organization","@id":"https:\/\/nebula.org\/blog\/fr\/#organization","name":"Nebula Genomics","url":"https:\/\/nebula.org\/blog\/fr\/","logo":{"@type":"ImageObject","inLanguage":"fr-FR","@id":"https:\/\/nebula.org\/blog\/fr\/#\/schema\/logo\/image\/","url":"","contentUrl":"","caption":"Nebula Genomics"},"image":{"@id":"https:\/\/nebula.org\/blog\/fr\/#\/schema\/logo\/image\/"},"sameAs":["https:\/\/facebook.com\/nebulagenomics","https:\/\/twitter.com\/nebulagenomics","https:\/\/www.instagram.com\/nebulagenomics\/","https:\/\/www.linkedin.com\/company\/nebula-genomics\/","https:\/\/en.wikipedia.org\/wiki\/Nebula_Genomics"]},{"@type":"Person","@id":"https:\/\/nebula.org\/blog\/fr\/#\/schema\/person\/3b2737c7f39b77815cfdbc95d95bc0c8","name":"Nikki Teran, B.S.","image":{"@type":"ImageObject","inLanguage":"fr-FR","@id":"https:\/\/nebula.org\/blog\/fr\/#\/schema\/person\/image\/","url":"https:\/\/nebula.org\/blog\/wp-content\/uploads\/2021\/01\/1535048906589-150x150.jpeg","contentUrl":"https:\/\/nebula.org\/blog\/wp-content\/uploads\/2021\/01\/1535048906589-150x150.jpeg","caption":"Nikki Teran, B.S."},"description":"Nikki Teran earned a B.S. in Molecular Biophysics and Biochemistry from Yale University. She is currently a Ph.D. Candidate in Genetics at Stanford University.\u00a0She has experience in technical writing at both Nebula Genomics and Ancestry DNA and scientific research experience as a Computation Biology intern at twoXar Pharmaceuticals.\u00a0Nikki is a member of the Montgomery lab at Stanford University. You can read more about Nikki's experience on LinkedIn and ORCID.","url":"https:\/\/nebula.org\/blog\/fr\/author\/nikki-teran\/"}]}},"_links":{"self":[{"href":"https:\/\/nebula.org\/blog\/fr\/wp-json\/wp\/v2\/posts\/9377","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/nebula.org\/blog\/fr\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/nebula.org\/blog\/fr\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/nebula.org\/blog\/fr\/wp-json\/wp\/v2\/users\/16"}],"replies":[{"embeddable":true,"href":"https:\/\/nebula.org\/blog\/fr\/wp-json\/wp\/v2\/comments?post=9377"}],"version-history":[{"count":0,"href":"https:\/\/nebula.org\/blog\/fr\/wp-json\/wp\/v2\/posts\/9377\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/nebula.org\/blog\/fr\/wp-json\/wp\/v2\/media\/35975"}],"wp:attachment":[{"href":"https:\/\/nebula.org\/blog\/fr\/wp-json\/wp\/v2\/media?parent=9377"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/nebula.org\/blog\/fr\/wp-json\/wp\/v2\/categories?post=9377"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/nebula.org\/blog\/fr\/wp-json\/wp\/v2\/tags?post=9377"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}