yes doing variant calling. But using samtools and bcftools, so it is different in this pipleine. I will run both pipelines. I wanna know what should be used in human?
Hi, I ran bcftools in the following way: bcftools mpileup -O b -o ${3}-${basename}.bcf -f $asm $bam bcftools call --ploidy 2 -m -o ${3}-${basename}.vcf ${3}-${basename}.bcf …
Hello, Sorry for this naive question, but I'm starting a RNAseq differential expression analysis, and it's my first time with human data. I'm wondering which …
Does that mean you are doing variant calling using GATK or similar? Ploidy = 2, or diploid, is the same.
yes doing variant calling. But using samtools and bcftools, so it is different in this pipleine. I will run both pipelines. I wanna know what should be used in human?