Thanks for writing this tool, this is a lifesaver. This is not a bug but a question.
I'm trying to use sam2tsv to output intersecting bases of all the reads for the given reference genome position in the --regions file. My command looks like this:
This is outputting all the bases of intersecting reads, I am wondering how to limit the output only to the intersecting positions. I could filter this by writing a Python script, since sam2tsv is generating enormous files and I have 100s of samples, I am wondering is there a way out?
Hello,
Thanks for writing this tool, this is a lifesaver. This is not a bug but a question.
I'm trying to use sam2tsv to output intersecting bases of all the reads for the given reference genome position in the --regions file. My command looks like this:
java -jar ~/jvarkit/dist/sam2tsv.jar -R sequence.fasta --regions snvs.vcf.gz aligned.bam
This is outputting all the bases of intersecting reads, I am wondering how to limit the output only to the intersecting positions. I could filter this by writing a Python script, since sam2tsv is generating enormous files and I have 100s of samples, I am wondering is there a way out?