MyPrompt$ /home/wdlin/Tools/bedtools2/bin/bedtools coverage -d -s -split -abam sample.bam -b Ppatens_152_chromosome.gff3 | ./coverage.pl new
MyPrompt$ /home/wdlin/Tools/bedtools2/bin/bedtools genomecov -ibam sample.bam -d -split -strand + | perl -ne 'chomp; @token=split; print "$token[-1]\n"' > old.scaffold_1.coverage.txt
MyPrompt$ diff new.scaffold_1.coverage.txt old.scaffold_1.coverage.txt
1028201c1028201
< 6
---
> 5 -split Treat "split" BAM or BED12 entries as distinct BED intervals.
when computing coverage.
For BAM files, this uses the CIGAR "N" and "D" operations
to infer the blocks for computing coverage.
For BED12 files, this uses the BlockCount, BlockStarts, and BlockEnds
fields (i.e., columns 10,11,12).
Thank you in advanced.
Wendar
--
You received this message because you are subscribed to the Google Groups "bedtools-discuss" group.
To unsubscribe from this group and stop receiving emails from it, send an email to bedtools-discu...@googlegroups.com.
For more options, visit https://groups.google.com/d/optout.
<sample.bam><coverage.pl><Ppatens_152_chromosome.gff3>