I created two vcf files using gatk and samtools. Now I want to detect overlapped variation to remove false positives. How can I detect overlapped variation?
Good evening, everyone. I've been working on a pipeline to convert FASTQ files obtained from RNA-seq into VCF files, but I'm having trouble getting it …
I have a bam file called `contaminated_sample.bam`, that was created (for dilution experiment) by mixing proportional amount of reads from two original bam files (`Sample_A.bam` …