Article

Color Data v2: a user-friendly, open-access database with hereditary cancer and hereditary cardiovascular conditions datasets

2020-01-15

Abstract excerpt

<h4>ABSTRACT</h4> Publicly-available genetic databases promote data sharing and fuel scientific discoveries for the prevention, treatment, and management of disease. In 2018, we built Color Data, a user-friendly, open access database containing genotypic and self-reported phenotypic information from 50,000 individuals who were sequenced for 30 genes associated with hereditary cancer. In a continued effort to prom...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: ac103aa9-9aad-5e68-b7e0-3c3bce4161af
DOI: 10.1101/2020.01.15.907212

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

Color Data v2: a user-friendly, open-access database with hereditary cancer and hereditary cardiovascular conditions datasetsDOI 10.1101/2020.01.15.907212Read

Color Data v2: a user-friendly, open-access database with hereditary cancer and hereditary cardiovascular conditions datasets.Semantic proximity Read

Development of an Open Database of Genes Included in Hereditary Cancer Genetic Testing Panels Available From Major Sources in the US.Semantic proximity Read

BRCAIndica: a Resource for ACMG/AMP classified BRCA1 and BRCA2 VariantsSemantic proximity Read

Gene2Phenotype: A Database of Structured Human Monogenic Diseases and Pathomechanisms.Semantic proximity Read

Understanding the genetic epidemiology of hereditary breast cancer in India using whole genome data from 1029 healthy individualsSemantic proximity Read

Systematic common and rare variant association testing in 392,030 whole genomes in <i>All of Us</i>Semantic proximity Read

ACMG Secondary Findings in the Brazilian Rare Genomes Project: Insights from 5,402 genome sequencingSemantic proximity Read

BRCAIndica: a resource for ACMG/AMP classified BRCA1 and BRCA2 variants.Semantic proximity Read

SpadaHC: a database to improve the classification of variants in hereditary cancer genes in the Spanish population.Semantic proximity Read

HeartBioPortal2.0: new developments and updates for genetic ancestry and cardiometabolic quantitative traits in diverse human populationsSemantic proximity Read

DIVAS: a centralized genetic variant repository representing 150,000 individuals from multiple disease cohorts.Semantic proximity Read

HeartBioPortal2.0: new developments and updates for genetic ancestry and cardiometabolic quantitative traits in diverse human populations.Semantic proximity Read