Nebula Genomics customers get access to the Nebula Library, a weekly updated collection of personalized reports based on the latest genetic discoveries. It empowers our users to stay up to date with the latest research in human genetics and learn how it applies to them. Today, the Nebula Library includes over 200 genome-wide association studies (GWAS) and new reports are added every week. To access your personalized Nebula Library, you need to purchase our Whole Genome Sequencing (or upload existing DNA data to get partial access). However, we also made the content of the Nebula Library publicly available here to help you discover reports that interest you.
STUDY TITLE: Genome-wide association identifies seven loci for pelvic organ prolapse in Iceland and the UK Biobank SUMMARY: Identification of 8 genetic variants associated with pelvic organ prolapse. OVERVIEW: The muscles that support a woman’s pelvic organs can weaken, causing …
STUDY TITLE: The genetic architecture of the human cerebral cortex SUMMARY: Identification of over 250 genetic loci associated with cortical surface area. OVERVIEW: The cerebral cortex is the outer layer of the brain that is responsible for cognitive tasks such as perception, …
STUDY TITLE: Identification of novel breast cancer susceptibility loci in meta-analyses conducted among Asian and European descendants SUMMARY: Discovery of 28 novel genomic regions associated with breast cancer risk. OVERVIEW: Breast cancer is the second most commonly diagnosed cancer in …
STUDY TITLE: A meta-analysis of genome-wide association studies identifies multiple longevity genes SUMMARY: Identification of multiple genetic variants associated with human longevity. DESCRIPTION: The average human lifespan has increased significantly over the past two centuries. However, genetic factors that determine …
Nebula Genomics DNA Report for Thyroid Cancer Is thyroid cancer genetic? We created a DNA report based on a study that attempted to answer this question. Below you can see a SAMPLE DNA report. To get your personalized DNA report, …
STUDY TITLE: Significance of the Myxovirus Resistance A (MxA) Gene — 123C>A Single-Nucleotide Polymorphism in Suppressed Interferon β Induction of Severe Acute Respiratory Syndrome Coronavirus Infection SUMMARY: Identification of a genetic variant associated with a decreased risk of SARS coronavirus infection. OVERVIEW: …
STUDY TITLE: Polymorphisms of interferon-inducible genes OAS-1 and MxA associated with SARS in the Vietnamese population SUMMARY: Discovery of a genetic variant in the OAS-1 gene associated with increased risk of severe acute respiratory syndrome (SARS) coronavirus infection. OVERVIEW: In 2003, severe …
STUDY TITLE: Functional polymorphisms of the CCL2 and MBL genes cumulatively increase susceptibility to severe acute respiratory syndrome coronavirus infection SUMMARY: Identification of 2 genetic variants associated with an increased risk of severe acute respiratory syndrome (SARS) coronavirus infection. OVERVIEW: Severe acute respiratory syndrome (SARS) coronavirus emerged in …
STUDY TITLE: Common genetic variants influence human subcortical brain structures SUMMARY: This study identified novel genetic variants that may influence the subcortical brain structures which are involved in complex activities including movement, emotions, and learning. DESCRIPTION: The subcortical region consists …
STUDY TITLE: Discovery of common and rare genetic risk variants for colorectal cancer SUMMARY: Genetic variants in genes involved in transcription, cell signaling, and the immune system are associated with the risk of colorectal cancer. DESCRIPTION: Colorectal cancer occurs in …
