Okay, here is my attempt at a qucik perlscript to do this (see attachment). Hope some perl expert can make it less clumsy!
Unconfigured Ad
Collapse
X
-
-
Hello,
I am working with RNASEq data and we are to use 2 sets of 3 bam files each, i.e. 2 different conditions and 3 replicates per condition (which were obtained using Tophat2) with Cufflinks, Cuffmerge and finally Cuffdiff.
Cuffmerge requires a txt file with the full paths to the (in this case 6) transcripts.gtf files which was obtained on running cufflinks on each of the bam files. It also requires a reference genome fasta file and a gtf annotation file.
I chose to use gencode's latest version 'gencode.v12.annotation.gtf' with cuffmerge. I however am getting the following error, and I don't have an answer for it.
[Wed Jul 4 00:53:50 2012] Preparing output location ./merged_asm/
[Wed Jul 4 00:55:46 2012] Converting GTF files to SAM
[00:57:34] Loading reference annotation.
Error: duplicate GFF ID 'ENST00000361547.2' encountered!
[FAILED]
Error: could not execute gtf_to_sam
Traceback (most recent call last):
File "/share/apps/assembly/bin/cuffmerge", line 576, in ?
sys.exit(main())
File "/share/apps/assembly/bin/cuffmerge", line 554, in main
sam_input_files = convert_gtf_to_sam(gtf_input_files)
File "/share/apps/assembly/bin/cuffmerge", line 287, in convert_gtf_to_sam
sam_out = gtf_to_sam(line)
File "/share/apps/assembly/bin/cuffmerge", line 247, in gtf_to_sam
exit(1)
TypeError: 'str' object is not callable
Does anyone know what this means, or why it is happening? Can it be fixed? Any help would be greatly appreciated. Thanks
- Vinay
Comment
Latest Articles
Collapse
-
by SEQadmin2
Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?
Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating...-
Channel: Articles
10-14-2026, 09:55 AM -
-
by SEQadmin2
Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.
We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing...-
Channel: Articles
-
ad_right_rmr
Collapse
News
Collapse
| Topics | Statistics | Last Post | ||
|---|---|---|---|---|
|
Started by SEQadmin2, Yesterday, 11:13 AM
|
0 responses
18 views
0 reactions
|
Last Post
by SEQadmin2
Yesterday, 11:13 AM
|
||
|
Started by SEQadmin2, Yesterday, 10:48 AM
|
0 responses
18 views
0 reactions
|
Last Post
by SEQadmin2
Yesterday, 10:48 AM
|
||
|
Started by SEQadmin2, 10-15-2026, 10:52 AM
|
0 responses
36 views
0 reactions
|
Last Post
by SEQadmin2
10-15-2026, 10:52 AM
|
||
|
Started by SEQadmin2, 10-14-2026, 05:39 AM
|
0 responses
42 views
0 reactions
|
Last Post
by SEQadmin2
10-14-2026, 05:39 AM
|
Comment