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Thread | Thread Starter | Forum | Replies | Last Post |
tophat problem: no accepted_hits.bam generated | RNAer | Bioinformatics | 9 | 08-30-2013 10:41 AM |
Tophat - accepted_hits.sam file is empty? | madsen | Bioinformatics | 42 | 08-01-2013 08:26 AM |
tophat problem: no accepted_hits.bam generated | RNAer | Bioinformatics | 0 | 07-19-2011 01:18 PM |
Split accepted_hits.bam file after Tophat run? | hong_sunwoo | Bioinformatics | 6 | 10-18-2010 01:06 AM |
tophat accepted_hits.sam file | Mark | Bioinformatics | 1 | 09-23-2009 04:33 PM |
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#1 |
Member
Location: India Join Date: Oct 2010
Posts: 14
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Folks..!
I've been running tophat since a couple of weeks and I've seen no success so far ![]() I have colorspace transcriptome data having 97 million reads. I've built Bowtie colorspace index as well. When I run tophat everything works fine, no error displays. The run completed perfectly all right; however, the output accepted_hits.bam file is COMPLETELY empty. The junctions.bed file is fine and is of 1.7 MB. ![]() On the other hand if I take 500,000 reads dataset from this same data, there is no error at all and it gives bam file that too not empty..!! ![]() Here is the command prompt and output display that tophat shows: $ tophat -G refgene_main.gtf --color --quals /color_index/oceano_c Solid97M_F3.csfasta Solid97M_F3_QV.qual [Mon Nov 15 18:14:47 2010] Beginning TopHat run (v1.1.2) ----------------------------------------------- [Mon Nov 15 18:14:47 2010] Preparing output location ./tophat_out/ [Mon Nov 15 18:14:47 2010] Checking for Bowtie index files [Mon Nov 15 18:14:47 2010] Checking for reference FASTA file [Mon Nov 15 18:14:47 2010] Checking for Bowtie Bowtie version: 0.12.7.0 [Mon Nov 15 18:14:47 2010] Checking for Samtools Samtools version: 0.1.9.0 [Mon Nov 15 18:14:47 2010] Checking reads min read length: 50bp, max read length: 50bp format: fasta [Mon Nov 15 18:22:18 2010] Reading known junctions from GFF file Warning: TopHat did not find any junctions in GFF file [Mon Nov 15 18:46:59 2010] Mapping reads against oceano_c with Bowtie [Mon Nov 15 20:47:35 2010] Joining segment hits [Mon Nov 15 21:32:26 2010] Mapping reads against oceano_c with Bowtie(1/2) [Mon Nov 15 22:10:52 2010] Mapping reads against oceano_c with Bowtie(2/2) [Mon Nov 15 22:45:59 2010] Searching for junctions via segment mapping [Mon Nov 15 23:10:36 2010] Retrieving sequences for splices [Mon Nov 15 23:10:51 2010] Indexing splices [Mon Nov 15 23:30:30 2010] Mapping reads against segment_juncs with Bowtie [Tue Nov 16 02:11:44 2010] Mapping reads against segment_juncs with Bowtie [Tue Nov 16 03:58:20 2010] Joining segment hits [Tue Nov 16 04:34:25 2010] Reporting output tracks ----------------------------------------------- Run complete [11:07:08 elapsed] Looks so good, isn't it? ![]() the logs folder is fine except one file "accepted_hits_sam_to_bam.log" where it shows "fail to open "./tophat_out/tmp/accepted_hits.sam" for reading" even though the folder has chmod 777 permissions ??????? ![]() Any help please? Any help is much appreciated ![]() |
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#2 |
Member
Location: College Park Join Date: Oct 2010
Posts: 27
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I just sent you an email. One thing you can try is to use "--keep-tmp" option not to delete the temporary files including tmp/accepted_hit.sam, and taking a look at them will probably give you some hints about what's going on there.
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Tags |
solid, tophat, tophat bowtie, transcriptome analysis |
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