{"id":13551,"date":"2021-01-31T22:14:47","date_gmt":"2021-02-01T03:14:47","guid":{"rendered":"https:\/\/nebula.org\/blog\/tornando-a-ciencia-acessivel-a-todos\/"},"modified":"2021-02-20T20:43:23","modified_gmt":"2021-02-21T01:43:23","slug":"tornando-a-ciencia-acessivel-a-todos","status":"publish","type":"post","link":"https:\/\/nebula.org\/blog\/pt-br\/tornando-a-ciencia-acessivel-a-todos\/","title":{"rendered":"Tornando a ci\u00eancia acess\u00edvel a todos"},"content":{"rendered":"\n<h3 class=\"wp-block-heading\"><strong>N\u00f3s ouvimos voc\u00ea!<\/strong><\/h3>\n\n<p>Come\u00e7amos a Nebula Genomics para capacitar as pessoas a desbloquear seus genomas e aprender sobre si mesmas. Para conseguir isso, temos que explicar a ci\u00eancia de ponta da forma mais simples poss\u00edvel. Muitos de voc\u00eas nos escreveram com perguntas sobre seus resultados e nos forneceram coment\u00e1rios \u00fateis. Temos ouvido e levando isso a s\u00e9rio. Nesta postagem do blog, gostar\u00edamos de apresentar algumas mudan\u00e7as na Nebula Library que fizemos recentemente com base em seus coment\u00e1rios.<br\/><\/p>\n\n<h3 class=\"wp-block-heading\"><strong>Explica\u00e7\u00f5es mais simples<\/strong><\/h3>\n\n<p>Simplificamos e esclarecemos as descri\u00e7\u00f5es dos estudos e pontua\u00e7\u00f5es polig\u00eanicas. Primeiro, todas as entradas da biblioteca agora t\u00eam novos t\u00edtulos que descrevem a caracter\u00edstica que foi investigada no estudo de forma muito mais clara<strong> (Figura 1A)<\/strong> . Em segundo lugar, melhoramos as descri\u00e7\u00f5es das pontua\u00e7\u00f5es e percentis polig\u00eanicos. Agora deve ser mais f\u00e1cil entender o que significam percentis altos e baixos<strong> (B)<\/strong> e como eles se relacionam com pontua\u00e7\u00f5es polig\u00eanicas<strong> (C)<\/strong> . Terceiro, para facilitar a compreens\u00e3o de nossas descri\u00e7\u00f5es de estudo, criamos uma funcionalidade de dicion\u00e1rio. Ao passar o mouse sobre os termos sublinhados, voc\u00ea ver\u00e1 as explica\u00e7\u00f5es desses termos aparecerem<strong> (D)<\/strong> .<\/p>\n\n<figure class=\"wp-block-image\"><img decoding=\"async\" src=\"https:\/\/lh6.googleusercontent.com\/bQzrvCheJfI4DZ1ucoSByu-EzrWzNOZ2hOe9-C_O29VAMf4djLjtXFfsbDsa7If4biINUdgfhHBeLzzC4jsJnmU78JAXM1rLvSI6lv6spa2YdE-Ko1RfkWueZkXuF2wlj0DBIqUh\" alt=\"\"\/><figcaption>Figura 1. Altera\u00e7\u00f5es e novos recursos na Nebula Library.<\/figcaption><\/figure>\n\n<h3 class=\"wp-block-heading\"><strong>Descoberta Facilitada<\/strong><\/h3>\n\n<p>Al\u00e9m de explicar melhor as coisas, adicionamos dois novos recursos que o ajudar\u00e3o a explorar seus resultados. Em primeiro lugar, agora voc\u00ea pode adicionar estudos que considere particularmente interessantes para o seu \u201c<strong> Favoritos<\/strong> \u201dClicando na estrela ao lado do t\u00edtulo do estudo<strong> (E)<\/strong> . Em segundo lugar, para ajud\u00e1-lo a encontrar estudos rec\u00e9m-adicionados mais facilmente, agora os marcamos como \u201c<strong> Novo<\/strong> \u201d<strong> (F)<\/strong> .<\/p>\n\n<h3 class=\"wp-block-heading\"><strong>Novo relat\u00f3rio em breve<\/strong><\/h3>\n\n<p>Enquanto estamos melhorando nossos relat\u00f3rios atuais, tamb\u00e9m estamos nos preparando para lan\u00e7ar relat\u00f3rios novos e expandidos para usu\u00e1rios que adquiriram nosso sequenciamento do genoma completo 30x. Estamos particularmente entusiasmados com nossas novas ferramentas de explora\u00e7\u00e3o. Muitos de voc\u00eas nos fizeram perguntas sobre como testar genes diferentes, pesquisar variantes espec\u00edficas e ler seus arquivos de dados gen\u00f4micos. Percebemos que nossos usu\u00e1rios est\u00e3o interessados em coisas diferentes e n\u00e3o h\u00e1 um \u00fanico relat\u00f3rio que se adapte a todos. Nossas novas ferramentas de explora\u00e7\u00e3o de dados tornar\u00e3o nossos relat\u00f3rios muito mais din\u00e2micos e dar\u00e3o a voc\u00ea o poder de encontrar uma resposta para qualquer d\u00favida que possa ter sobre o seu DNA. Confira nossa p\u00e1gina de produto para saber mais sobre nosso novo<a href=\"https:\/\/nebula.org\/whole-genome-sequencing\/\"><strong> Servi\u00e7o de sequenciamento de genoma completo 30x<\/strong><\/a> !<\/p>\n","protected":false},"excerpt":{"rendered":"<p>N\u00f3s ouvimos voc\u00ea! Come\u00e7amos a Nebula Genomics para capacitar as pessoas a desbloquear seus genomas e aprender sobre si mesmas. Para conseguir isso, temos que explicar a ci\u00eancia de ponta da forma mais simples poss\u00edvel. Muitos de voc\u00eas nos escreveram &hellip;<\/p>\n<p class=\"read-more\"> <a class=\"ast-button\" href=\"https:\/\/nebula.org\/blog\/pt-br\/tornando-a-ciencia-acessivel-a-todos\/\"> <span class=\"screen-reader-text\">Tornando a ci\u00eancia acess\u00edvel a todos<\/span> Leia mais \u00bb<\/a><\/p>\n","protected":false},"author":11,"featured_media":13555,"comment_status":"closed","ping_status":"open","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":"","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":[5004],"tags":[],"class_list":["post-13551","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-news-pt-br"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v20.13 - 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