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Changes to UMI processing #1937
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maxulysse
reviewed
Aug 14, 2025
Co-authored-by: Maxime U Garcia <max.u.garcia@gmail.com>
SPPearce
commented
Aug 15, 2025
nh13
reviewed
Aug 28, 2025
maxulysse
approved these changes
Sep 8, 2025
FriederikeHanssen
approved these changes
Sep 8, 2025
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Big set of changes to UMI processing.
Currently the only UMI processing is through generating consensus reads using fgbio, which is inefficient for whole genome sequencing.
Often the UMI might have already been extracted into the read header (such as through bclconvert) or maybe in the bam file already.
Introduces:
samtoolsrather thansamblasterto do the merge and sort, as is done in the fastquorum pipeline; this removes samblaster entirely (I couldn't get samblaster to merge the multiple files in one go).umi_tagparameter is set.Note that long-term I think we should we just be sending people to fastquorum if they want consensus reads rather than implementing in sarek.