gpart: human genome partitioning and visualization of high-density SNP data by identifying haplotype blocks
Open Access
- 1 November 2019
- journal article
- research article
- Published by Oxford University Press (OUP) in Bioinformatics
- Vol. 35 (21) , 4419-4421
Abstract
For the analysis of high-throughput genomic data produced by next-generation sequencing (NGS) technologies, researchers need to identify linkage disequilibrium (LD) structure in the genome. In this work, we developed an R package gpart which provides clustering algorithms to define LD blocks or analysis units consisting of SNPs. The visualization tool in gpart can display the LD structure and gene positions for up to 20 000 SNPs in one image. The gpart functions facilitate construction of LD blocks and SNP partitions for vast amounts of genome sequencing data within reasonable time and memory limits in personal computing environments. The R package is available at https://bioconductor.org/packages/gpart. Supplementary data are available at Bioinformatics online.Keywords
Funding Information
- National Research Foundation of Korea
- NRF (NRF-2018R1A2B6008016)
- Canadian Institutes of Health Research
- CIHR (MOP-84287, PJT 159463)
- Canadian Statistical Sciences Institute
- Canadian Institutes of Health Research Strategic Training for Advanced Genetic Epidemiology (GET-101831)
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