Entering edit mode
4.8 years ago
Susmita Mandal
▴
110
Hi,
I trimmed my paired end fastq data using Trimmomatic using TruSeq-PE adapters, but actually they contain Nextera transposase adapter sequences. I have already aligned and did variant calling using GATK "HaplotypeCaller". Would the adapter contamination will affect the variant calling?
Please help me out.
Thanks,
Susmita
How many reads are affected? Run
fastqc
on the bam files to find out.