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Thread | Thread Starter | Forum | Replies | Last Post |
Mixed read lengths in TopHat input file | shurjo | Bioinformatics | 13 | 11-01-2012 05:46 AM |
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Platform comparison of read lengths | ryantkoehler | General | 0 | 10-05-2009 09:37 AM |
How to visualise alignments with different read lengths? | lindseyjane | Bioinformatics | 5 | 09-17-2009 02:27 AM |
Pacific Bio releases some details on SMRT Sequencer read lengths, library prep | ECO | The Pipeline | 6 | 10-15-2008 01:54 PM |
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#1 |
Member
Location: Woods Hole, Massachusetts Join Date: Jul 2010
Posts: 16
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I am working with SOLiD data and have trimmed reads. I am trying to calculate the length of the reads and their number. I have seen several publications where they have shown these details.
My question is, do you calculate them using linux commands? or is there any other efficient way to do it. Any hints will be highly appreciated. Thank you |
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#2 |
Senior Member
Location: Germany Join Date: Oct 2008
Posts: 415
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If you have base space fasta files have a look at the tool Galaxy online. There are tonnes of other tools which should do this for you. R may also be useful for you.
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