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4.6 years ago
netsam
▴
10
Hi, I tried to assemble a set of reads directly from a BAM file with Velvet in Galaxy Australia. The reads seems to cover the entire reference sequence of about 1.000 bp, but the assembling failed. I attach an IGB screenshot.
The BAM file was generated with BWA-MEM, inside Galaxy wrapper
Please post galaxy related questions to Galaxy help site for prompt help.
In this case you may want to reach out to Galaxy australia support.
Instead of the image hosting provider you are using please use these directions: How to add images to a Biostars post