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gpart: human genome partitioning and visualization of high-density SNP data by identifying haplotype blocks.
Kim, Sun Ah; Brossard, Myriam; Roshandel, Delnaz; Paterson, Andrew D; Bull, Shelley B; Yoo, Yun Joo.
Afiliação
  • Kim SA; The Research Institute of Basic Sciences, Seoul National University, Seoul, South Korea.
  • Brossard M; Prosserman Centre for Health Research, The Lunenfeld-Tanenbaum Research Institute, Sinai Health System, Toronto, ON, Canada.
  • Roshandel D; Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada.
  • Paterson AD; Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada.
  • Bull SB; Division of Biostatistics, Dalla Lana School of Public Health, University of Toronto, Toronto, ON, Canada.
  • Yoo YJ; Prosserman Centre for Health Research, The Lunenfeld-Tanenbaum Research Institute, Sinai Health System, Toronto, ON, Canada.
Bioinformatics ; 35(21): 4419-4421, 2019 11 01.
Article em En | MEDLINE | ID: mdl-31070701
ABSTRACT

SUMMARY:

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. AVAILABILITY AND IMPLEMENTATION The R package is available at https//bioconductor.org/packages/gpart. SUPPLEMENTARY INFORMATION Supplementary data are available at Bioinformatics online.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Genoma Humano / Polimorfismo de Nucleotídeo Único Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Genoma Humano / Polimorfismo de Nucleotídeo Único Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article