 | 1 | initial version |
I looked around but could not find the answer. I think this question would benefit others so I ask here. I import VCF files from whole exome and gene panel analysis. I want to "activate" variants that are within coordinates specified in a BED file and see some statistics for features in this BED file (i.e. number of variants per feature, coverage per gene). Currently the closest result I can get is the "Variant Classification Count by Gene" report. But it gives report for all genes in the gene track hence shadows the regions of my interest.
Is there a script or trick to get this done?
Thanks
| | 2 | No.2 Revision |
I looked around but could not find the answer. I think this question would benefit others so I ask here. I import VCF files from whole exome and gene panel analysis. I want to "activate" variants that are within coordinates specified in a BED file and see some statistics for features in this BED file (i.e. number of variants per feature, coverage per gene). Currently the closest result I can get is the "Variant Classification Count by Gene" report. But it gives report for all genes in the gene track hence shadows the regions of my interest.
Is there a script or trick to get this done?
Thanks
