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3.5 years ago
deniselavezzari
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0
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
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.