Hi,
I have a question related to the steps following a liftOver.
Since there is no annotation available for rhesus macaque genome for the last assemblies, I did a lift over of rheMac2 (the old assembly) annotations to the recent rheMac8 assembly (using STAR). I obtained two output files, one with all the features that have been lifted over, with the new coordinates, and one with the "unmapped" features.
But I didn't find any clear explanation of what is the next step (maybe it's trivial...).
Can I directly use this output file as my annotation file to index my rheMac3 genome and do the alignment? (I'm using STAR for this)
Second question: is there a statistic I can look at to say how well my lift over worked? I looked at how many features ended up in the liftover file vs unmapped file, and 97% of the features present in the original annotation have been lifted over. Is that enough to say I can use this reliably?
I didn't find a source clearly explaining this, but if you know one, any link is welcome :)
Thank you,
Camille
genome
alignment
rna-seq