Closed vymao closed 4 years ago
Hi,
I am interested in running VarDict on WGS samples. I tried running it without a BED file for b37 but I get no variants called (I only see a VCF header). When I tried running VarDict on targeted panel sequencing with a BED file, it worked fine.
This was the command I used:
AF_THR="0.01" tumor_sample_name=$1 tumor_bam=$2 normal_sample_name=$3 normal_bam=$4 vardict -G /path/to/b37/human_g1k_v37_decoy.fasta -f $AF_THR -N ${tumor_sample_name}\ -b "${tumor_bam}|${normal_bam}" | testsomatic.R | var2vcf_paired.pl -N\ "${tumor_sample_name}|${normal_sample_name}" -f $AF_THR
Is a BED file necessary? If so, how can we get one for b37?
Hi Viktor, I answered to issue in VarDictJava repository, so I'll close this one!
Hi,
I am interested in running VarDict on WGS samples. I tried running it without a BED file for b37 but I get no variants called (I only see a VCF header). When I tried running VarDict on targeted panel sequencing with a BED file, it worked fine.
This was the command I used:
Is a BED file necessary? If so, how can we get one for b37?