Hi everyone,
I'm new in bioinformatics field. I'd like to know how to and which are the best tools for local realignment around indels. I have fastq files coming from MiSeq (Illumina) as pipeline input and I'm performing the bioinformatic pipeline using python (and running tools from comand line). I should perform local realignment only after PCR duplicates removal? And which tool should I use to first identify indels around which local realignment will be done?
Thanks in advance, Elisa
I was calling the variants with bcftools. Do you suggest me to use GATK4 instead? (I have a targeted sequencing problem with tumor samples)
when publishing it's (sadly?) better to say you used the "GATK best practices" to call your variants...