Hi,
I would like to know if there is any functions in Bioconductor (or other) that
could help me calculate the alignable portion of a genome (not human), given a
reference sequence.
When I say alignable portion I mean that I want to know all the positions of
the genome that can be covered uniquely by reads of 36 bp and up to 2
mismatches.
Best regards,
João
[[alternative HTML version deleted]]
_______________________________________________
Bioc-sig-sequencing mailing list
[email protected]
https://stat.ethz.ch/mailman/listinfo/bioc-sig-sequencing
