loading
LiteratureBiomedical imagesGene informationOthers
Gerstein Lab Structural & Copy Number Variations logo

A portal collecting several downloadable tools for the study of genomic structural & copy number variations. Software tools can be used to construct a personal diploid genome sequence by including personal variants into reference genome (vcf2diploid), to discover and genotype CNVs from genome sequencing (CNVnator), etc. Registration not required.



Published on 2013-10-12 06:04:54 - Click here to edit or to add informations - Report as not working

<< PLINK - Whole genome association analysis toolset >> GSEA




We use cookies. By browsing our site you agree to our use of cookies. Accept cookies Find out more