I have WGS 10x coverage paired-end fastq files and I want to call CNVs on these files. I aligned the files using bwa, and called lumpy traditional on it, but somehow lumpy is not calling the required CNVs. We know the genes where the variants occur. Could you please help me with this.
Hi @ryanlayer,
I have WGS 10x coverage paired-end fastq files and I want to call CNVs on these files. I aligned the files using bwa, and called lumpy traditional on it, but somehow lumpy is not calling the required CNVs. We know the genes where the variants occur. Could you please help me with this.
Thank you