Hi,

It says on https://cgwb.nci.nih.gov/goldenPath/help/hgTracksHelp.html,

"When the number of lines within a requested track location exceeds
250, the track automatically defaults to a more tightly-packed display
mode. In this situation, you can restore the track display to full
mode by narrowing the chromosomal range displayed or by using a track
filter to reduce the number of items displayed."

In bam flle where the sequencing depth is high, it is likely to have
more 250 reads in a locus. Therefore, no matter how narrow the chrom
range is selected, there will be more than 250 reads. Does anybody
know how to filter a bam track?

-- 
Regards,
Peng
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