My library is single-fragment size, 310bp. Does this situation be suitble to the methods you mentioned?
how to align sequences with extra bases in 5'
Hi, my sequecing data contains 30 extra base pairs in the 5' which also contain UMI information. First, I want to map these reads to a reference genome and then I want to stastics the UMI information. How should I set mapping defaults? Does 30 extra bps interfere the mapping process?
My UMI information is not in the start point of a reads. They are 30bp away from 5'.
Thanks for your answers.
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The simplest thing to do is use umi-tools to pull the umi off of the read, and put it in the read name. Then align as usual, and then run mi-tools to go through the bam and remove excess reads based on map position and umi sequence
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