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.
Original language | English |
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Pages (from-to) | 2496-2497 |
Number of pages | 1 |
Journal | Bioinformatics |
Volume | 30 |
Issue number | 17 |
DOIs | |
Publication status | Published - 1 Sept 2014 |