Closed lpryszcz closed 8 years ago
If you use the "SNPCoverage" track type instead of "FeatureCoverage", then it is easier to see the spliced alignments. Not totally what you want though.
Alternatively, you can generate bigwig files to indicate coverage. Using a pipeline of BAM->BedGraph->BigWig is pretty good with the combination of "bedtools genomecov" with the BAM file as input (make sure to use the -split option), and "bedGraphToBigWig" to make the conversion to bigwig http://bedtools.readthedocs.org/en/latest/content/tools/genomecov.html
http://gmod.827538.n3.nabble.com/Gmod-ajax-Question-on-Read-and-coverage-Display-td4051758.html
Thanks Colin! Actually, I do have bigwig track with correct coverage. Just wanted to report there is an issue with that, but I see you are already aware of it.
I've noticed coverage is wrongly displayed from BAM files for spliced alignments. You expect no or lower coverage for introns than for exons.
http://zdglab.iimcb.gov.pl/jbrowse/?data=data%2FGRCz10&tracks=DNA%2Cgene%2CmRNA%2CRZE024_bam_cov%2CRZE024_bam&loc=5%3A23582706..23585281&highlight=