Detailed overview:
Title: HaploReg
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Creator: Harvard University <Cambridge, Mass.> / BROAD Institute; MIT = Massachusetts Institute of Technology <Cambridge, Mass.>
Abstract: HaploReg is a tool for exploring annotations of the noncoding genome at variants on haplotype blocks, such as candidate regulatory SNPs at disease-associated loci. Using LD information from the 1000 Genomes Project, linked SNPs and small indels can be visualized along with their predicted chromatin state in nine cell types, conservation across mammals, and their effect on regulatory motifs. HaploReg is designed for researchers developing mechanistic hypotheses of the impact of non-coding variants on clinical phenotypes and normal variation. [Information of the supplier]
Subject: Biochemical genetics (572.8)
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Audience: Intermediate; Experts
Language: English
Format: database
Resource type: Factual databases
Access: free
Metadata update date: 2012-08-30
Metadata provider: UBFfm
URL of this vifabio-resource:
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