Open dollinad opened 4 years ago
Hi,
We have used Platypus to call somatic variants by using the following command on Linux - Centos7
python Platypus.py callVariants --genSNPs=1 --genIndels=0 -o path_to_output --refFile=hg38_no_alt.fa --bamFiles=tumor_bam,normal_bam --nCPU=5
The above command generates a vcf file with over 5 million variants which is much more than other tools we have tested using the same sample.
I was wondering if there is a way to only call somatic variants or flter the germline variants.
Thanks, Dollina
Hi,
We have used Platypus to call somatic variants by using the following command on Linux - Centos7
python Platypus.py callVariants --genSNPs=1 --genIndels=0 -o path_to_output --refFile=hg38_no_alt.fa --bamFiles=tumor_bam,normal_bam --nCPU=5
The above command generates a vcf file with over 5 million variants which is much more than other tools we have tested using the same sample.
I was wondering if there is a way to only call somatic variants or flter the germline variants.
Thanks, Dollina