Recents studies in mammalian genomes have uncovered the extent of copy number variation (CNV) that contributes to phenotypic diversity, including health and disease status. Here we report the first gl
Support file to run miXer tool for calling CNV from WES data. miXer tool is available at https://github.com/ctglab/miXer and at https://hub.docker.com/r/ctglabcnr/mixer
Recents studies in mammalian genomes have uncovered the extent of copy number variation (CNV) that contributes to phenotypic diversity, including health and disease status. Here we report the first gl
