Re: [galaxy-user] Running Cufflinks on Bacterial RNAseq data

2012-08-01 Thread Peter Cock
On Tue, Jul 31, 2012 at 7:35 PM, Jennifer Jackson j...@bx.psu.edu wrote: Hello Rachel, When datasets are in a grey waiting to run state this indicates that they are in the queue and in line to run. For the majority of cases, including yours, leaving the job alone and allowing it to run is the

Re: [galaxy-user] Running Cufflinks on Bacterial RNAseq data

2012-08-01 Thread Jennifer Jackson
Peter is correct (I oversimplified)! And Cufflinks does allow for an ID attribute to span lines as long as it represents the same feature. To be clear, this error was a true format issue. The best way to understand the finer points is to see the specification (also linked from wiki below):

Re: [galaxy-user] Running Cufflinks on Bacterial RNAseq data

2012-07-31 Thread Jennifer Jackson
Hello Rachel, When datasets are in a grey waiting to run state this indicates that they are in the queue and in line to run. For the majority of cases, including yours, leaving the job alone and allowing it to run is the correct option. The missing metadata only means that the result has not

[galaxy-user] Running Cufflinks on Bacterial RNAseq data

2012-07-27 Thread Rachel Krasich
I am attempting to run Cufflinks on Galaxy main to analyze my E. coli RNAseq data. I have mapped my reads using an outside program (Genious) and uploaded the resulting BAM file. I also have uploaded the E. coli annotations as a gtf file. However when I attempt to run Cufflinks using my

[galaxy-user] Running cufflinks on a genome without a bowtie index

2011-12-22 Thread Noa Sher
Hi I am trying to run Cufflinks on a genome without a bowtie index. How do I make my own index? I have a FASTA file of the genome, but if I run tophat using just that and then cufflinks using a gtf file of the transcriptome, I get zero in all FPKM values Thanks

Re: [galaxy-user] Running cufflinks on a genome without a bowtie index

2011-12-22 Thread Jeremy Goecks
Noa, Using your FASTA in Tophat and Cufflinks is the correct approach. You don't need to provide an annotation file in Cufflinks, and you can also avoid using your FASTA in Cufflinks by not using bias correction. If you're still having problems, the issue is likely your parameter choices in

Re: [galaxy-user] running cufflinks

2011-09-07 Thread Peter Cock
On Tue, Sep 6, 2011 at 9:29 PM, Peng, Tao tp...@fhcrc.org wrote: Hi I had 3 GTF files from ensemble, UCSC and NCBI for annotation; ONLY ensemble were recognized by GALAXY cufflinks as a GTF file although they all have .GTF. I am NOT sure why UCSC and NCBI GTF files were seen as GFF files?

Re: [galaxy-user] running cufflinks

2011-09-06 Thread Peng, Tao
Hi I had 3 GTF files from ensemble, UCSC and NCBI for annotation; ONLY ensemble were recognized by GALAXY cufflinks as a GTF file although they all have .GTF. I am NOT sure why UCSC and NCBI GTF files were seen as GFF files? Thx, tao -Original Message- From: Jennifer Jackson

[galaxy-user] running cufflinks

2011-09-06 Thread Jennifer Jackson
=== Please use Reply All when responding to this email=== Hello, File type can be set by using a dataset's pencil icon to reach the Edit Attributes form. GTF and GFF are both very similar. It is possible that the 9th field (group for GFF, attributes for GTF) was not detected automatically

[galaxy-user] running cufflinks

2011-09-01 Thread Jennifer Jackson
=== Please use Reply All when responding to this email === Hello, This is the same reply as for the bug report, but for others who may run into the same problem job that fails with this error: terminate called after throwing an instance of 'std::bad_alloc' what(): std::bad_alloc the

[galaxy-user] running cufflinks

2011-09-01 Thread Peng, Tao
Hi I am NOT sure why running cufflinks failed here. Thanks for your suggestion, tao --- Tool: Cufflinks Name: Cufflinks on data 6 and data 26: assembled transcripts Created:Sep 01, 2011 Filesize: 81.3 Mb Dbkey: hg19 Format: gtf Tool Version: Input