Closed GrossTor closed 2 years ago
The Cross-species regulatory sequence activity prediction project uses bigwig tracks from the mouse cell atlas. Those were generated from ATACseq reads that were aligned to the mm9 genome assembly. However, basenji tries to predict those tracks from the sequence of the mm10 genome assembly (other mouse tracks e.g. from Fantom5 are aligned to mm10 as well).
Could you explain how this discrepancy was resolved? I see multiple solutions:
What would you recommend?
That's correct. Crossmap seems good. I converted to bedgraph, then used UCSC liftover.
Makes sense. Thank you!
The Cross-species regulatory sequence activity prediction project uses bigwig tracks from the mouse cell atlas. Those were generated from ATACseq reads that were aligned to the mm9 genome assembly. However, basenji tries to predict those tracks from the sequence of the mm10 genome assembly (other mouse tracks e.g. from Fantom5 are aligned to mm10 as well).
Could you explain how this discrepancy was resolved? I see multiple solutions:
What would you recommend?