snpEnrichR: analyzing co-localization of SNPs and their proxies in genomic regions

A1 Originalartikel i en vetenskaplig tidskrift (referentgranskad)


Interna författare/redaktörer


Publikationens författare: Nousiainen K, Kanduri K, Ricano-Ponce I, Wijmenga C, Lahesmaa R, Kumar V, Lahdesmaki H
Förläggare: OXFORD UNIV PRESS
Publiceringsår: 2018
Tidskrift: Bioinformatics
Tidskriftsakronym: BIOINFORMATICS
Volym: 34
Artikelns första sida, sidnummer: 4112
Artikelns sista sida, sidnummer: 4114
Antal sidor: 3
ISSN: 1367-4803


Abstrakt

Motivation: Co-localization of trait associated SNPs for specific transcription-factor binding sites or regulatory regions in the genome can yield profound insight into underlying causal mechanisms. Analysis is complicated because the truly causal SNPs are generally unknown and can be either SNPs reported in GWAS studies or other proxy SNPs in their linkage disequilibrium. Hence, a comprehensive pipeline for SNP co-localization analysis that utilizes all relevant information about both the genotyped SNPs and their proxies is needed.Results: We developed an R package snpEnrichR for SNP co-localization analysis. The software integrates different tools for random SNP generation and genome co-localization analysis to automatize and help users to create custom SNP co-localization analysis. We show via an example that including proxy SNPs in SNP co-localization analysis enhances the sensitivity of co-localization detection.

Senast uppdaterad 2019-17-11 vid 04:29