I'm aware that you have to stick to the same reference genome during the whole analysis. I.e., if the analysis started with hg19, you have to stick to that to not introduce inconsistencies.
However, is it the same with releases for the same assembly?
If you have mapped the reads to e.g grch38.p13 release 32, and a new update is released e.g, grch38.p13 release 43, which is the newest. Can you change to that without having to remap the reads to get new bam files? What if you change from grch38.p12 to grch38.p13?
As far as I have understood, the gene coordinates are not changed in these releases. Can someone please clarify what is correct here, Im so confused π
Thanks in advance!
Patch releases do not change main chromosome coordinates. So you don't need to worry about that for normal analysis as in you will not need to remap the reads. If you were working with
alt
regions,haplotypes
then those would be added/amended in each patch.That said it is best to stay with a consistent reference (patch and all) for one set of analyses.
Great, thx for you straight forward answer!