Tuesday, April 20, 2010

OpenHelix: Search results for query '"copy number variation"'

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DGV: Database of Genomic Variants: http://projects.tcag.ca/variation/
The Database of Genomic Variants, DGV: curated data on structural variation in the human genome, focused on CNVs (Copy Number Variations), and a powerful genome browser

UCSC Genome Browser: http://genome.ucsc.edu/
UCSC Genome Browser, genome mapping, sequence, expression, comparative genomics, and analysis tools and portal to ENCODE project

GBrowse: http://gmod.org/wiki/Gbrowse
The Generic Genome Browser is a combination of flexible database and interactive Web page tools for visualizing, manipulating and displaying annotations on genomes

VISTA: http://genome.lbl.gov/vista/index.shtml
VISTA, comparative analysis tools for alignment and visualization of genomic sequences

HapMap: http://hapmap.org/
A multi-country consortium project to identify and catalog human genetic variation and catalog the SNPs

Genetics Home Reference: http://ghr.nlm.nih.gov/
Genetics Home Reference, or GHR: detailed information on genes, genetic variability, chromosomes, and their relationship to human diseases and conditions

GVS: http://gvs.gs.washington.edu/GVS/
GVS, Genome Variation Server: tool to access and analyze human genotype data from dbSNP and HapMap

FlyBase: http://flybase.org/
FlyBase, Drosophila genomic database and analysis tools

Atlas of Genetics and Cytogenetics in Oncology and Haematology: http://atlasgeneticsoncology.org/
Peer-reviewed genetic and cytogenetic-related oncology and haematology, information including genes, chromosomes, literature, links and educational sources - a comprehensive cancer research tool

dbERGE II: http://www.bx.psu.edu/
dbERGE II, gene expression database

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