I was wondering if you had considered merging UMIs that might be erroneous copies, eg as outlined in this blog post.
The use of UMIs [...] would work perfectly if it were not for base-calling errors, which erroneously create sequencing reads with the same genomic coordinates and UMIs and that are identical for the base at which the error occurred.
If I understand the current code correctly, it considers two barcodes as separte UMIs if they differ even by one base. Would it be useful to merge reads into the same UMI if they are 'nearly' identical, e.g. based on Hamming distance?
I was wondering if you had considered merging UMIs that might be erroneous copies, eg as outlined in this blog post.
If I understand the current code correctly, it considers two barcodes as separte UMIs if they differ even by one base. Would it be useful to merge reads into the same UMI if they are 'nearly' identical, e.g. based on Hamming distance?