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SNPLINK:纳入自动连锁不平衡消除的密集分布SNP数据的多点连锁分析。

SNPLINK: multipoint linkage analysis of densely distributed SNP data incorporating automated linkage disequilibrium removal.

作者信息

Webb Emily L, Sellick Gabrielle S, Houlston Richard S

机构信息

Section of Cancer Genetics, Institute of Cancer Research 15 Cotswold Road, Sutton, Surrey SM2 5NG, UK.

出版信息

Bioinformatics. 2005 Jul 1;21(13):3060-1. doi: 10.1093/bioinformatics/bti449. Epub 2005 Apr 19.

Abstract

SNPLINK is a Perl script that performs full genome linkage analysis of high-density single nucleotide polymorphism (SNP) marker sets. The presence of linkage disequilibrium (LD) between closely spaced SNP markers can falsely inflate linkage statistics. SNPLINK removes LD from the marker sets in an automated fashion before carrying out linkage analysis. SNPLINK can compute both parametric and non-parametric statistics, utilizing the freely available Allegro and Merlin software. Graphical outputs of whole genome multipoint linkage statistics are provided allowing comparison of results before and after the removal of LD.

摘要

SNPLINK是一个Perl脚本,用于对高密度单核苷酸多态性(SNP)标记集进行全基因组连锁分析。紧密间隔的SNP标记之间存在连锁不平衡(LD),可能会错误地夸大连锁统计量。在进行连锁分析之前,SNPLINK会以自动化方式从标记集中去除LD。SNPLINK可以利用免费的Allegro和Merlin软件计算参数统计量和非参数统计量。提供全基因组多点连锁统计的图形输出,以便比较去除LD前后的结果。

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