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Thread | Thread Starter | Forum | Replies | Last Post |
Wrong exon number information from tophat-fusion | angerusso | RNA Sequencing | 0 | 02-07-2014 10:46 AM |
Does tophat use the library-type information for mapping, or just for the XS flag? | carmeyeii | Bioinformatics | 1 | 05-16-2013 11:18 AM |
How to add in the right read group information when running Tophat? | Clare S | RNA Sequencing | 0 | 04-17-2013 09:13 PM |
tophat + cufflinks: strand information | Zimbobo | Bioinformatics | 29 | 04-20-2012 12:35 AM |
tophat islands information | syslm01 | Bioinformatics | 0 | 08-11-2010 03:48 AM |
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#1 |
Member
Location: us Join Date: Apr 2016
Posts: 14
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Hi all!
I used tophat2 with the option -G in order to give the gtf file but the output reported the chromosome coordinate. Why? What did I get wrong? How can I obtain the gene information? Thank you in advance |
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#2 |
Devon Ryan
Location: Freiburg, Germany Join Date: Jul 2011
Posts: 3,480
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tophat2 will always produce alignments in genomic coordinates. If you want alignments in transcriptome coordinates, then use bowtie2 or something similar to align against the transcriptome.
You might also use salmon, sailfish, or Kallisto, which will produce expression metrics directly (I assume that's what you need) and be vastly faster. |
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#3 | |
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Location: us Join Date: Apr 2016
Posts: 14
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#4 |
Devon Ryan
Location: Freiburg, Germany Join Date: Jul 2011
Posts: 3,480
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You could do that, for example with featureCounts or htseq-count (or bedtools intersect or ...). The question is only what you want to do with the results.
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#5 |
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Location: us Join Date: Apr 2016
Posts: 14
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Thank you (again) for your answer. I am using Ribosome profiling data and I need to have the SAM file with the name gene, position on the gene and the sequence.
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#6 |
Devon Ryan
Location: Freiburg, Germany Join Date: Jul 2011
Posts: 3,480
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There are already tools for Ribosomal profiling, just use them. Have a look at ribogalaxy (http://ribogalaxy.ucc.ie/) for an example of tools.
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Tags |
gene annotation, gtf file, tophat 2 |
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