Abstract
Summary: We created a fast, robust and general C++ implementation of a single-nucleotide polymorphism (SNP) set enrichment algorithm to identify cell types, tissues and pathways affected by risk loci. It tests trait-Associated genomic loci for enrichment of specificity to conditions (cell types, tissues and pathways). We use a non-parametric statistical approach to compute empirical P-values by comparison with null SNP sets. As a proof of concept, we present novel applications of our method to four sets of genome-wide significant SNPs associated with red blood cell count, multiple sclerosis, celiac disease and HDL cholesterol. © The Author 2014. Published by Oxford University Press. All rights reserved.
Cite
CITATION STYLE
Slowikowski, K., Hu, X., & Raychaudhuri, S. (2014). SNPsea: An algorithm to identify cell types, tissues and pathways affected by risk loci. Bioinformatics, 30(17), 2496–2497. https://doi.org/10.1093/bioinformatics/btu326
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