One of the concerns I am trying to resolve is that I have a bam file which I am trying to visualise on galaxy.
But it doesn't seem to render.
I have used "Reference genome build (dbkey): Human Feb. 2009 (GRCh37/hg19) (hg19)"
But get "no data for this chrom/contig." as a display message.
Ultimately we would like to be able to get a VCF file or even better still an essential changes file where known SNPs have been filtered out and any polymorphism have been checked for possible changes to amino acid sequence.
I am new to Galaxy and still exploring what it can do so correct me if it can't perform what I would like it to do.
Thank you for any help you can provide.
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Sen Res Tech to Professor Bhattacharya
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Office: +44 (0) 207 608 6951
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