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Is it possible to get BAM/SAM output from the tool instead of FASTQ? I guess my purposes are kind of weird but I just wanted to get the read pair info without re-alignment
The text was updated successfully, but these errors were encountered:
Hi, I agree that it would be useful to get BAM/SAM output from the tool. For reads that map to a certain region I would like to know where the other read is mapped.
Is it possible to get BAM/SAM output from the tool instead of FASTQ? I guess my purposes are kind of weird but I just wanted to get the read pair info without re-alignment
The text was updated successfully, but these errors were encountered: