A database providing rapid access to human genotype data and analysis tools.
Tutorial and training materials by OpenHelix
|Learn to use GVS (Genome Variation Server), a comprehensive database that provides quick access to all data found in both the dbSNP and HapMap databases and includes specialized data from other projects. The database includes a suite of analysis tools such as linkage disequilibrium plots, tag SNPs, merging populations, and more. In addition you can upload our own data and use the GVS analysis and visualization tools. If your research involves genetic variation and SNPs, learn how to use this valuable tool for your analysis needs.|
- to search for variation by keyword or by sequence
- to obtain haplotype, linkage disequilibrium and other types of variation data
- to download specific and targeted data
This tutorial is a part of the tutorial group UW SNP resources. You might find the other tutorials in the group interesting:
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Recent BioMed Central research articles citing this resource
Gottlieb Bruce et al., Changing genetic paradigms: creating next-generation genetic databases as tools to understand the emerging complexities of genotype/phenotype relationships. Human Genomics (2014) doi:10.1186/1479-7364-8-9
Jeannin Guido et al., Recurrent exercise-induced acute renal failure in a young Pakistani man with severe renal hypouricemia and SLC2A9 compound heterozygosity Clinical-Molecular Genetics and Cytogenetics. BMC Medical Genetics (2014) doi:10.1186/1471-2350-15-3
Vihinen Mauno et al., Variation ontology: annotator guide. Journal of Biomedical Semantics (2014) doi:10.1186/2041-1480-5-9
Klein Artjom et al., Benchmarking infrastructure for mutation text mining. Journal of Biomedical Semantics (2014) doi:10.1186/2041-1480-5-11
Fanis Pavlos et al., Genotyping of BCL11A and HBS1L-MYB SNPs associated with fetal haemoglobin levels: a SNaPshot minisequencing approach Human and rodent genomics. BMC Genomics (2014) doi:10.1186/1471-2164-15-108
More about the resource:
Genome Variation Server (GVS) is a database hosted by the SeattleSNPs Program for Genomic Applications (PGA), which works to identify, genotype and model the associations between SNPs in candidate genes. GVS is funded as part of the National Heart Lung and Blood Institute's (NHLBI) Programs for Genomic Applications (PGA).
The materials and slides offered can not be resold or used for profit purposes. Reproduction, distribution and/or use is strictly limited to instructional purposes only and can not be used for for monetary gain or wide distribution.
Copyright 2009, OpenHelix, LLC.