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Thread | Thread Starter | Forum | Replies | Last Post |
SOLiD QV plot | av_d | SOLiD | 5 | 07-19-2012 11:22 PM |
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coverage plot | golharam | Bioinformatics | 23 | 10-07-2010 01:43 PM |
Plot graph | gopu_36 | Bioinformatics | 1 | 11-15-2009 11:37 PM |
Anyone seen an intensity plot like this? | sequencer_lee | Illumina/Solexa | 7 | 07-11-2008 11:57 AM |
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#1 |
Junior Member
Location: Spain Join Date: Mar 2012
Posts: 1
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Hi everybody,
I'm using VarScan2's Somatic Mutation Calling function and the output are two files with a large number of columns. I wanna represent graphically two columns (normal_var_freq(column 7) and tumor_var_freq(column 11)) form one of both with R and it was impossible for me. It is driving me mad! If someone could help me, or tell me something about this, I'd be very gratefull! Thanks in advance. |
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#2 |
Senior Member
Location: Paris Join Date: Aug 2011
Posts: 239
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One idea is to keep only the mutations in which you are interested by using a bash script, for example somatic or LOH.
But if you are interested in germline mutations, you won't maybe be able to read everything in R because that are the more frequent mutations... |
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