The variant call format and VCFtools
The variant call format (VCF) is a generic format for storing DNA polymorphism data such as
SNPs, insertions, deletions and structural variants, together with rich annotations. VCF is …
SNPs, insertions, deletions and structural variants, together with rich annotations. VCF is …
The international HapMap project
…, JTF Wong, RL Nussbaum, SF Schaffner, ST Sherry… - 2003 - deepblue.lib.umich.edu
The goal of the International HapMap Project is to determine the common patterns of DNA
sequence variation in the human genome and to make this information freely available in the …
sequence variation in the human genome and to make this information freely available in the …
dbSNP: the NCBI database of genetic variation
ST Sherry, MH Ward, M Kholodov, J Baker… - Nucleic acids …, 2001 - academic.oup.com
In response to a need for a general catalog of genome variation to address the large-scale
sampling designs required by association studies, gene mapping and evolutionary biology, …
sampling designs required by association studies, gene mapping and evolutionary biology, …
Database resources of the national center for biotechnology information
…, GD Schuler, E Sequeira, ST Sherry… - Nucleic acids …, 2010 - academic.oup.com
In addition to maintaining the GenBank® nucleic acid sequence database, the National
Center for Biotechnology Information (NCBI) provides analysis and retrieval resources for the …
Center for Biotechnology Information (NCBI) provides analysis and retrieval resources for the …
[HTML][HTML] Database resources of the national center for biotechnology information
The National Center for Biotechnology Information (NCBI) produces a variety of online
information resources for biology, including the GenBank® nucleic acid sequence database and …
information resources for biology, including the GenBank® nucleic acid sequence database and …
The NCBI dbGaP database of genotypes and phenotypes
…, D Preuss, E Yaschenko, A Graeff, J Ostell, ST Sherry - Nature …, 2007 - nature.com
The National Center for Biotechnology Information has created the dbGaP public repository
for individual-level phenotype, exposure, genotype and sequence data and the associations …
for individual-level phenotype, exposure, genotype and sequence data and the associations …
[HTML][HTML] Database resources of the national center for biotechnology information
The National Center for Biotechnology Information (NCBI) provides a large suite of online
resources for biological information and data, including the GenBank® nucleic acid sequence …
resources for biological information and data, including the GenBank® nucleic acid sequence …
[HTML][HTML] ClinGen—the clinical genome resource
…, SE Plon, EM Ramos, ST Sherry… - … England Journal of …, 2015 - Mass Medical Soc
ClinGen — The Clinical Genome Resource | NEJM Skip to main content NEJM Group Follow Us
Facebook Twitter Instagram YouTube LinkedIn Prepare to become a physician, build your …
Facebook Twitter Instagram YouTube LinkedIn Prepare to become a physician, build your …
The genetic structure of ancient human populations
1. I990. A century of change in the Javanese rural economy: Contrasting developments in
upland and lowland Klaten. Internationales Asienforum 21: 259-77. 9. I93a. Actor and event …
upland and lowland Klaten. Internationales Asienforum 21: 259-77. 9. I93a. Actor and event …
dbSNP—database for single nucleotide polymorphisms and other classes of minor genetic variation
ST Sherry, M Ward, K Sirotkin - Genome research, 1999 - genome.cshlp.org
Akey aspect of research in genetics is associating sequence variations with heritable
phenotypes. The most common variations are single nucleotide polymorphisms (SNPs), which …
phenotypes. The most common variations are single nucleotide polymorphisms (SNPs), which …