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#1 |
Junior Member
Location: Germany Join Date: Feb 2017
Posts: 3
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Hi All.
I have zero experience with sequencing or sequencing files, so please excuse if I ask something stupid ![]() I just learned that colleague of mine needs to regularly do one and the same task - open .ab1 file with Chromas, cut 50 base pairs from the left, save and close it again. I wonder if there is any way to automate it. Command line tool, Python/R/java/dotnet library, anything like this. Any hints? I tired to google, but found it problematic to use the results I found, so I hope for advise. Thank you anyway for reading. Have a good day ![]() |
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#3 |
Junior Member
Location: Germany Join Date: Feb 2017
Posts: 3
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Thanks for reply.
The most discussion in the internet I found talks about converting AB1 to FASTA, looks like it much more common task than editing and saving ab1 itself. This 4peaks software is it scriptable? |
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#4 |
Member
Location: Louisiana Join Date: Nov 2013
Posts: 38
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sangerseqR can parse AB1 files. It doesn't have built in functions to cut 50bp, but you could probably cobble something together with Bioconductor.
http://bioconductor.org/packages/rel...angerseqR.html |
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#5 |
Junior Member
Location: Germany Join Date: Feb 2017
Posts: 3
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Thanks!
Cutting is not big deal I guess, but unfortunately I do not see any ABIF writing functionality there. But adding abif instead of abi to my queries I found Bio-Trace-ABIF perl package that also might be usefull Last edited by TaKo; 02-15-2017 at 08:31 AM. |
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Tags |
ab1, api, command line, library |
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