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