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y own, but I
wondered if anyone's dealt with this before.
Thanks for any advice, leads, etc. ...
~Joe
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Joseph Fass
Bioinformatics Data Analyst
UC Davis Genome Center - Bioinformatics Core
http://bioinformatics.ucdavis.edu/
jnf...@ucdavis.edu
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Joseph Fass
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UC Davis Genome Center - Bioinformatics Core
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Is there any interest in adding read alignment browsing to mauve? I.e. load
BAM files for each reference, and view all the read alignments at the same
time, anchored and gapped according to the multiple alignment between
genomes?
If not, is anyone aware of a tool that does this?
-Joe
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thought of using the
positions in the SNPs file, but that excludes gaps between LCBs and other
more complicated differences, right?
Any help would be appreciated ...
~Joe
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Joseph Fass
Lead Data Analyst
UC Davis Bioinformatics Core
http://bioinformatics.ucdavis.edu/
joseph.fass -at-
ile of the
currently-viewable sequence, with genome names and ranges (or chromosome
names and ranges? or both?). I'd find this very useful for a current
project, but I'm wondering if others would find it useful enough to clamor
for an added feature!
Thanks,
~Joe
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Joseph Fass
Lead Da
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auve-users mailing list
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