I have constructed a bigBed file from a BED file containing 50bp next gen. sequencing reads. However, when I try to view the bigBed file on UCSC I only get a single black bar in the track, presumably covering areas containing the 50bp reads. I.e. I am not seeing the individual reads, regardless of whether the track is set to 'full', 'squish' etc.
Also, when i try to view a chromosome worth of data from the BED file the same thing happens unless i zoom right in. Any experience or solutions to this? Many thanks! Ian _______________________________________________ Genome maillist - [email protected] https://lists.soe.ucsc.edu/mailman/listinfo/genome
