Question: Bam Files
0
Edward Dudley • 10 wrote:
Hi -
I have a set of 454 reads that have been trimmed and converted to BAM
format using Galaxy, and I can visualize the alignment with E. coli
genomes using the UCSC browser. Problem is, I'd like to display the
alignment in Artemis, but Artemis doesn't seem to want to read the
.BAM file downloaded from Galaxy; I can import my genome sequence but
when trying to import the BAM a blank window with "message" in the
header keeps popping up. Anyone else tried to do this, and is there
something about the Galaxy BAM files that Artemis doesn't like?
Thanks.
Ed
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modified 7.6 years ago
by
Loraine, Ann • 150
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written
7.6 years ago by
Edward Dudley • 10