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Showing 1 to 3 of 3 items tagged as genotype and phenotype


dbGaP- Database of Genotypes and Phenotypes

database

Provider: National Center for Biotechnology Information
Contents:
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Descriptions: In dbGaP, NCBI archives and distributes the results of studies investigating the interaction of genotype and phenotype. Genome-wide association studies, medical sequencing, molecular diagnostic assays, and associations between genotype and non-clinical traits are covered. dbGaP contains both open- and controlled-access data. Non-sensitive data are released on a broad scale, but sensitive data sets involving personal health information are not publicly accessible. Search by study or disease, or use Advanced Search.
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ALFRED: The Allele Frequency Database

database

Provider: Kenneth K. Kidd, Yale University / US National Science Foundation
Contents: , ,
Access Level:
Descriptions: "ALFRED's focus is on allele frequencies in diverse anthropologically defined populations. It is not a compendium of human DNA polymorphisms but of frequencies of selected polymorphisms with an emphasis on those that have been studied in multiple populations. All of the data in ALFRED are considered to be in the public domain and available for use in research and teaching."
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1000 Genomes

database

Provider: 1000 Genomes
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Access Level:
Descriptions: 1000 Genomes: a deep catalog of human genetic variation "...is the first project to sequence the genomes of a large number of people, to provide a comprehensive resource on human genetic variation... The goal of the 1000 Genomes Project is to find most genetic variants that have frequencies of at least 1% in the populations studied." 1000 Genomes is an international endeavor, with participants from institutes, governments and universities world-wide. "DNA from the samples will be available for researchers to follow up with more detailed studies of variation in particular regions. The cell lines will allow researches to study cellular phenotypes such as gene expression, epigenetic patterns, and drug response. The extensive genotype data available on the samples, and the trio samples for some of the populations, will allow researchers to map regions of the genome computationally that affect the cellular phenotypes, and to study the heritability of these phenotypes."
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