FAIRsharing record for: HaploReg
收藏Mendeley Data2024-01-31 更新2024-06-30 收录
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https://fairsharing.org/FAIRsharing.x18jh7
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资源简介：
This FAIRsharing record describes: 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 chromatin state and protein binding annotation from the Roadmap Epigenomics and ENCODE projects, sequence conservation across mammals, the effect of SNPs on regulatory motifs, and the effect of SNPs on expression from eQTL studies. HaploReg is designed for researchers developing mechanistic hypotheses of the impact of non-coding variants on clinical phenotypes and normal variation.
创建时间：
2024-01-31
