easyLINKAGE-Plus - automated linkage analyses using large-scale SNP data

被引:137
作者
Hoffmann, K
Lindner, TH
机构
[1] Humboldt Univ, Inst Med Genet, D-13353 Berlin, Germany
[2] Univ Wurzburg, Dept Med, D-97080 Wurzburg, Germany
[3] Univ Wurzburg, Med Clin, Dept Clin Biochem & Pathobiochem, D-97078 Wurzburg, Germany
关键词
D O I
10.1093/bioinformatics/bti571
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We extended the original easyLINKAGE program by enabling linkage analyses for large-scale SNP data in addition to those of microsatellites. We implemented new modules for Allegro, Merlin, SimWalk, GeneHunter Imprinting, GeneHunter TwoLocus, SuperLink and extended FastSLink by automatic loop breaking and new outputs. We added conditional linkage analyses as well as multipoint simulation studies, and extended error test routines by checking for Mendelian/non-Mendelian genotyping errors and for deviations from Hardy-Weinberg equilibrium. Data can be analyzed in sets of markers, in defined centimorgan intervals and by using different allele frequency algorithms. The outputs consist of genome-wide as well as chromosomal postscript plots of LOD scores, NPL scores, P-values and other parameters.
引用
收藏
页码:3565 / 3567
页数:3
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