SNPsea: An algorithm to identify cell types, tissues and pathways affected by risk loci

Kamil Slowikowski, Xinli Hu, Soumya Raychaudhuri

    Research output: Contribution to journalArticlepeer-review

    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 languageEnglish
    Pages (from-to)2496-2497
    Number of pages1
    JournalBioinformatics
    Volume30
    Issue number17
    DOIs
    Publication statusPublished - 1 Sept 2014

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