Hi all,
I'm new to the field so please forgive my ignorance. I setup Tophat, Bowtie, and SamTools and attempted to run tophat on some samples. This is the message it produced:
[2012-11-28 19:56:55] Beginning TopHat run (v2.0.6)
-----------------------------------------------
[2012-11-28 19:56:55] Checking for Bowtie
Bowtie 2 not found, checking for older version..
Bowtie version: 0.12.8.0
[2012-11-28 19:56:55] Checking for Samtools
Samtools version: 0.1.18.0
[2012-11-28 19:56:55] Checking for Bowtie index files
[2012-11-28 19:56:55] Checking for reference FASTA file
[2012-11-28 19:56:55] Generating SAM header for /u/home/mcdb/x/bowtie-0.12.8/indexes/genome
format: fastq
quality scale: phred64 (reads generated with GA pipeline version >= 1.3)
[2012-11-28 19:58:09] Reading known junctions from GTF file
[2012-11-28 19:58:21] Preparing reads
left reads: min. length=50, max. length=50, 75848803 kept reads (6201 discarded)
[2012-11-28 20:17:00] Creating transcriptome data files..
[FAILED]
Error: gtf_to_fasta returned an error.
open: No such file or directory
[main_samview] fail to open "R1/accepted_hits.bam" for reading.
cp: cannot stat `R1/accepted_hits.bam': No such file or directory
This is a different error than I first posted, sorry. I can't figure out why I am getting the gtf_to_fasta error. I downloaded Ensembl's NCBIM37 for mouse here: http://cufflinks.cbcb.umd.edu/igenomes.html. Then I used the mus_musculus gtf included in it, as well as the genome.ebwt files included in the BowtieIndex folder of the unpacked file. I read in another post that this error could be from the fasta and gtf files having different names, so I renamed them both genome but got the same error.
Any help is appreciated. Thanks!
I'm new to the field so please forgive my ignorance. I setup Tophat, Bowtie, and SamTools and attempted to run tophat on some samples. This is the message it produced:
[2012-11-28 19:56:55] Beginning TopHat run (v2.0.6)
-----------------------------------------------
[2012-11-28 19:56:55] Checking for Bowtie
Bowtie 2 not found, checking for older version..
Bowtie version: 0.12.8.0
[2012-11-28 19:56:55] Checking for Samtools
Samtools version: 0.1.18.0
[2012-11-28 19:56:55] Checking for Bowtie index files
[2012-11-28 19:56:55] Checking for reference FASTA file
[2012-11-28 19:56:55] Generating SAM header for /u/home/mcdb/x/bowtie-0.12.8/indexes/genome
format: fastq
quality scale: phred64 (reads generated with GA pipeline version >= 1.3)
[2012-11-28 19:58:09] Reading known junctions from GTF file
[2012-11-28 19:58:21] Preparing reads
left reads: min. length=50, max. length=50, 75848803 kept reads (6201 discarded)
[2012-11-28 20:17:00] Creating transcriptome data files..
[FAILED]
Error: gtf_to_fasta returned an error.
open: No such file or directory
[main_samview] fail to open "R1/accepted_hits.bam" for reading.
cp: cannot stat `R1/accepted_hits.bam': No such file or directory
This is a different error than I first posted, sorry. I can't figure out why I am getting the gtf_to_fasta error. I downloaded Ensembl's NCBIM37 for mouse here: http://cufflinks.cbcb.umd.edu/igenomes.html. Then I used the mus_musculus gtf included in it, as well as the genome.ebwt files included in the BowtieIndex folder of the unpacked file. I read in another post that this error could be from the fasta and gtf files having different names, so I renamed them both genome but got the same error.
Any help is appreciated. Thanks!
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