Tried opening it in libre office calc but the program just freezes
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I'm actually trying to write in python. How do I notate a certain variable in a sam file (I'm very new to python bioinformatics).Originally posted by dpryan View PostYou really don't want to write macros to deal with data of this size. Try python/perl/C/whatever. You can use R, if you prefer, but I think it usually reads everything into memory too.
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Generally something like the following will work:
So, just use the column number. You can also use pysam, which makes some things much easier. If you're comfortable with C, I can also recommend the samtools C API. If you need higher performance, you'll find it quite useful.Code:import csv sam = csv.reader(open("foo.sam","r"), dialect="excel-tab") for line in sam : print("QNAME: %s" % (line[0])) print("Sequence: %s" % (line[9]))
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So that's basically exactly what I was looking for. Thanks!Originally posted by dpryan View PostGenerally something like the following will work:
So, just use the column number. You can also use pysam, which makes some things much easier. If you're comfortable with C, I can also recommend the samtools C API. If you need higher performance, you'll find it quite useful.Code:import csv sam = csv.reader(open("foo.sam","r"), dialect="excel-tab") for line in sam : print("QNAME: %s" % (line[0])) print("Sequence: %s" % (line[9]))
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Right, I'll have to figure out some of the details. Right now, I just have an idea what I want to perform, but no real idea how to execute. But I did just read through a tutorial that kind of went over the sort of info you presented, I was just unaware that you could do this directly to a sam file.Originally posted by dpryan View PostGlad I could help. BTW, I didn't deal with the header in my example. You might check "if(len(line) > 5): stuff" or check for a @ as the first character to get past the header (unless you want to parse it).
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You might want to consider the pysam module: http://wwwfgu.anat.ox.ac.uk/~andreas...tools/api.html and https://code.google.com/p/pysam/
(EDIT: I see Devon already suggested this - apologies for the duplication0
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Visualize Bam
FYI: I wrote a simple java-based GUI to visualize some BAMS: https://github.com/lindenb/jvarkit/wiki/BamViewGui
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I’m not a sequencing expert. I’m a purification scientist who uses NGS to evaluate workflows my group develops. With this perspective, we think about the sample first and the NGS workflow second. The sequencer is an exceptionally honest reporter, but it can only report on what you give it, so whether you get clean, interpretable data from an NGS workflow is largely determined before you begin.
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Data variability is still an issue in sequencing technologies despite the advances in reproducibility and accuracy of these platforms. But the problem does not originate in the sequencing itself, but in the previous steps, before the sample reaches the sequencer.
The first step is collection, followed by preservation and sample preparation for analysis. Most scientists overlook those steps, but not being careful might just be skewing the experiment’s results.
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