How to analyze DNA data with UMI
Hi all!
I'm facing with analyze DNA exomes sequencing data with UMI. From the demultiplexing, I have three fastq files: one for reads R1, one for the UMI tags, and one for the R2. Now, I have to align data to the reference genome and call variants. Have you some suggestions for me?
Does anyone know some "best practices" for that?
Thanks
Denise
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Have you looked at documentation of standard software such as UMI-tools?
Also, see How to take in consideration UMI in WES pipeline?. By the way, Ian (the guy who answers this question) is the author of UMI-tools.