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When we run epinano, we divide the total number of sequences in the reference into several groups and then we subset the initial bam file. I've encountered that when using a transcriptome reference, it is possible that no reads are mapped to the subset of references and thus, epinano fails as the input is empty. How can we avoid this?
Thanks a lot!
The text was updated successfully, but these errors were encountered:
When we run epinano, we divide the total number of sequences in the reference into several groups and then we subset the initial bam file. I've encountered that when using a transcriptome reference, it is possible that no reads are mapped to the subset of references and thus, epinano fails as the input is empty. How can we avoid this?
Thanks a lot!
The text was updated successfully, but these errors were encountered: