Seqanswers Leaderboard Ad

Collapse

Announcement

Collapse
No announcement yet.
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • Gonza
    replied
    glad it worked!

    Leave a comment:


  • leejimmy93
    replied
    It turned out my problem was caused by the reference gtf/gff file too. Thank you very much!

    Leave a comment:


  • Gonza
    replied
    Hi,

    This is what i was getting.



    [Fri Jan 6 12:35:41 2017] Beginning transcriptome assembly merge

    -------------------------------------------

    [Fri Jan 6 12:35:41 2017] Preparing output location ./merged_asm/

    [Fri Jan 6 12:36:23 2017] Converting GTF files to SAM

    [12:36:23] Loading reference annotation.

    GFF Error: duplicate/invalid 'transcript' feature ID=Peaxi162Scf00002g00014.1

    [FAILED]

    Error: could not execute gtf_to_sam




    Once i started to used an updated GTF/GFF file i had no problem. Not sure what species you're working with, but this problem will not occur if you are using one with well annotated features.

    Good luck

    Leave a comment:


  • leejimmy93
    replied
    Originally posted by Gonza View Post
    Hi all,

    I am not sure if this is a 'universal' answer, but the problem i was running into was in the gtf file. Cufflinks does not deal well with duplicated genes ID. In my particular case, i was using an old gtf file that must have had duplicates. Once i used the most updated one, i had no problem.

    G
    Hi, do you mean the duplicated gene ID in the reference gtf file or the gtf file generated by cufflinks? Also was your reference gtf file sorted? Can you please send me a screenshot of the gtf file that works and that doesn't work?

    Thank you very much!

    Leave a comment:


  • Gonza
    replied
    Cufflinks duplicated genes error

    Hi all,

    I am not sure if this is a 'universal' answer, but the problem i was running into was in the gtf file. Cufflinks does not deal well with duplicated genes ID. In my particular case, i was using an old gtf file that must have had duplicates. Once i used the most updated one, i had no problem.

    G

    Leave a comment:


  • leejimmy93
    replied
    Did anyone fixed the problem? same problem happened here.

    Leave a comment:


  • bbm
    replied
    Anybody knows how to fix this?
    I ran into the same problem. I'm using cufflinks 2.2.1

    Leave a comment:


  • Gonza
    replied
    Hello All,

    I am having the same problem. Thanks for the help



    [Fri Aug 21 18:11:42 2015] Beginning transcriptome assembly merge
    -------------------------------------------

    [Fri Aug 21 18:11:42 2015] Preparing output location /home3/gonzalo/Petunia/03_cuffmerge/
    [Fri Aug 21 18:12:44 2015] Converting GTF files to SAM
    [18:12:44] Loading reference annotation.
    GFF Error: duplicate/invalid 'transcript' feature ID=Peaxi162Scf00001g00028.1
    [FAILED]
    Error: could not execute gtf_to_sam

    Leave a comment:


  • thickrick99
    replied
    Sorry to bring back an old thread but has anyone found a solution for this yet?? I posted in the RNA-seq forum and still have no replies but I am facing the same issue and can't seem to find a solution on the internet. Any ideas??

    Leave a comment:


  • gokhulkrishnakilaru
    replied
    Originally posted by ef10k View Post
    Thanks for the reply, damiankao. However, the fix that you described didn't work for me (by editing the cuffmerge script from v1.0.2 - as far as I can tell, the header sorting issue that your fix addresses has been resolved in v1.1.0).

    Specifically, the output that I get is:

    [Thu Sep 29 14:14:05 2011] Beginning transcriptome assembly merge
    -------------------------------------------

    [Thu Sep 29 14:14:05 2011] Preparing output location transcripts_merge/
    [Thu Sep 29 14:14:19 2011] Converting GTF files to SAM
    [14:14:19] Loading reference annotation.
    [FAILED]
    Error: could not execute gtf_to_sam


    Poking around in the cuffmerge script, one can see that the error is generated by this function:

    Code:
    def gtf_to_sam(gtf_filename):
    
        sam_out = tmp_name("gtf2sam_")
    
        cmd = ["gtf_to_sam"]
        cmd.append("-F")
        cmd.append(gtf_filename)
        cmd.append(sam_out)
        try:
            print >> run_log, " ".join(cmd)
            ret = subprocess.call(cmd)
            if ret != 0:
                print >> sys.stderr, fail_str, "Error: could not execute gtf_to_sam"
                exit(1)
    However, I really don't know much about python and don't have a good idea of what this is doing. Does anyone have any ideas about what's going wrong here?
    Change your
    cmd = ["gtf_to_sam"]
    to
    cmd = ["/path_of the_program/gtf_to_sam"]

    Leave a comment:


  • gpertea
    replied
    It turns out there is a trivial fix for at least some of the crashes reported here (just increasing the cigar[] buffer size in gtf_to_sam.cpp and recompile). Until the next official Cufflinks package release, those affected by this problem can use these patched binaries to replace the gtf_to_sam program that came with the 1.1.0 distribution:

    For Mac OSX:
    ftp://ftp.cbcb.umd.edu/pub/software/..._to_sam.OSX.gz

    For Linux x86_64:
    ftp://ftp.cbcb.umd.edu/pub/software/...o_sam.Linux.gz

    (please remember to rename the file to gtf_to_sam after decompressing it)

    The patched source code is here:
    ftp://ftp.cbcb.umd.edu/pub/software/misc/gtf_to_sam.cpp

    Leave a comment:


  • dweebis
    replied
    Hi Guys -

    I'm having essentially the same problem. I'm trying to merger together just two transcript.gtf files usig the following command:

    >cuffmerge -s ~/Work/genomes/Homo_sapiens/UCSC/hg19/Sequence/WholeGenomeFasta/genome.fa assemblies.txt
    And I get the following output:
    [Mon Oct 24 15:18:45 2011] Beginning transcriptome assembly merge
    -------------------------------------------

    [Mon Oct 24 15:18:45 2011] Preparing output location ./merged_asm/
    Warning: no reference GTF provided!
    [Mon Oct 24 15:18:49 2011] Converting GTF files to SAM
    [15:18:49] Loading reference annotation.
    *** buffer overflow detected ***: gtf_to_sam terminated
    ======= Backtrace: =========
    /lib/libc.so.6(__fortify_fail+0x37)[0x7f52eb7e8217]
    /lib/libc.so.6(+0xfe0d0)[0x7f52eb7e70d0]
    /lib/libc.so.6(+0xfcf87)[0x7f52eb7e5f87]
    gtf_to_sam[0x406fb0]
    gtf_to_sam[0x408c84]
    gtf_to_sam[0x409226]
    /lib/libc.so.6(__libc_start_main+0xfd)[0x7f52eb707c4d]
    gtf_to_sam[0x406ab9]
    ======= Memory map: ========
    00400000-004f3000 r-xp 00000000 08:01 8260509 /usr/local/cufflinks-1.1.0/bin/gtf_to_sam
    006f2000-006f3000 r--p 000f2000 08:01 8260509 /usr/local/cufflinks-1.1.0/bin/gtf_to_sam
    006f3000-006f5000 rw-p 000f3000 08:01 8260509 /usr/local/cufflinks-1.1.0/bin/gtf_to_sam
    006f5000-00700000 rw-p 00000000 00:00 0
    00e06000-096ea000 rw-p 00000000 00:00 0 [heap]
    7f52eb4e1000-7f52eb4e8000 r-xp 00000000 08:01 9178866 /lib/librt-2.11.1.so
    7f52eb4e8000-7f52eb6e7000 ---p 00007000 08:01 9178866 /lib/librt-2.11.1.so
    7f52eb6e7000-7f52eb6e8000 r--p 00006000 08:01 9178866 /lib/librt-2.11.1.so
    7f52eb6e8000-7f52eb6e9000 rw-p 00007000 08:01 9178866 /lib/librt-2.11.1.so
    7f52eb6e9000-7f52eb863000 r-xp 00000000 08:01 9178850 /lib/libc-2.11.1.so
    7f52eb863000-7f52eba62000 ---p 0017a000 08:01 9178850 /lib/libc-2.11.1.so
    7f52eba62000-7f52eba66000 r--p 00179000 08:01 9178850 /lib/libc-2.11.1.so
    7f52eba66000-7f52eba67000 rw-p 0017d000 08:01 9178850 /lib/libc-2.11.1.so
    7f52eba67000-7f52eba6c000 rw-p 00000000 00:00 0
    7f52eba6c000-7f52eba84000 r-xp 00000000 08:01 9178864 /lib/libpthread-2.11.1.so
    7f52eba84000-7f52ebc83000 ---p 00018000 08:01 9178864 /lib/libpthread-2.11.1.so
    7f52ebc83000-7f52ebc84000 r--p 00017000 08:01 9178864 /lib/libpthread-2.11.1.so
    7f52ebc84000-7f52ebc85000 rw-p 00018000 08:01 9178864 /lib/libpthread-2.11.1.so
    7f52ebc85000-7f52ebc89000 rw-p 00000000 00:00 0
    7f52ebc89000-7f52ebc9f000 r-xp 00000000 08:01 9175119 /lib/libgcc_s.so.1
    7f52ebc9f000-7f52ebe9e000 ---p 00016000 08:01 9175119 /lib/libgcc_s.so.1
    7f52ebe9e000-7f52ebe9f000 r--p 00015000 08:01 9175119 /lib/libgcc_s.so.1
    7f52ebe9f000-7f52ebea0000 rw-p 00016000 08:01 9175119 /lib/libgcc_s.so.1
    7f52ebea0000-7f52ebf22000 r-xp 00000000 08:01 9178854 /lib/libm-2.11.1.so
    7f52ebf22000-7f52ec121000 ---p 00082000 08:01 9178854 /lib/libm-2.11.1.so
    7f52ec121000-7f52ec122000 r--p 00081000 08:01 9178854 /lib/libm-2.11.1.so
    7f52ec122000-7f52ec123000 rw-p 00082000 08:01 9178854 /lib/libm-2.11.1.so
    7f52ec123000-7f52ec219000 r-xp 00000000 08:01 5901999 /usr/lib/libstdc++.so.6.0.13
    7f52ec219000-7f52ec419000 ---p 000f6000 08:01 5901999 /usr/lib/libstdc++.so.6.0.13
    7f52ec419000-7f52ec420000 r--p 000f6000 08:01 5901999 /usr/lib/libstdc++.so.6.0.13
    7f52ec420000-7f52ec422000 rw-p 000fd000 08:01 5901999 /usr/lib/libstdc++.so.6.0.13
    7f52ec422000-7f52ec437000 rw-p 00000000 00:00 0
    7f52ec437000-7f52ec44d000 r-xp 00000000 08:01 9175234 /lib/libz.so.1.2.3.3
    7f52ec44d000-7f52ec64c000 ---p 00016000 08:01 9175234 /lib/libz.so.1.2.3.3
    7f52ec64c000-7f52ec64d000 r--p 00015000 08:01 9175234 /lib/libz.so.1.2.3.3
    7f52ec64d000-7f52ec64e000 rw-p 00016000 08:01 9175234 /lib/libz.so.1.2.3.3
    7f52ec64e000-7f52ec662000 r-xp 00000000 08:01 5937267 /usr/lib/libboost_thread.so.1.40.0
    7f52ec662000-7f52ec861000 ---p 00014000 08:01 5937267 /usr/lib/libboost_thread.so.1.40.0
    7f52ec861000-7f52ec863000 r--p 00013000 08:01 5937267 /usr/lib/libboost_thread.so.1.40.0
    7f52ec863000-7f52ec864000 rw-p 00015000 08:01 5937267 /usr/lib/libboost_thread.so.1.40.0
    7f52ec864000-7f52ec884000 r-xp 00000000 08:01 9178847 /lib/ld-2.11.1.so
    7f52eca5d000-7f52eca63000 rw-p 00000000 00:00 0
    7f52eca7f000-7f52eca83000 rw-p 00000000 00:00 0
    7f52eca83000-7f52eca84000 r--p 0001f000 08:01 9178847 /lib/ld-2.11.1.so
    7f52eca84000-7f52eca85000 rw-p 00020000 08:01 9178847 /lib/ld-2.11.1.so
    7f52eca85000-7f52eca86000 rw-p 00000000 00:00 0
    7fff7d7fe000-7fff7d81f000 rw-p 00000000 00:00 0 [stack]
    7fff7d9ff000-7fff7da00000 r-xp 00000000 00:00 0 [vdso]
    ffffffffff600000-ffffffffff601000 r-xp 00000000 00:00 0 [vsyscall]
    [FAILED]
    Error: could not execute gtf_to_sam
    I get essentially the same error running gtf_to_sam directly. System call failures are out of my depth, has there been any more progress on this problem?

    Leave a comment:


  • SEQond
    replied
    did the Cufflinks website GTF solve the problem?

    Leave a comment:


  • ZhengXia
    replied
    As damiankao said, maybe you can try the gtf provided in the Cufflinks website.
    Originally posted by damiankao View Post
    It looks like the gtf_to_sam script is not working. Do you have it in your path? Have you tried merging only the cufflinks gtf outputs together? Maybe the USCS gtf is not formatted in a way that cuffmerge can read? You can try running gtf_to_sam on a gtf file without cuffmerge and see if that works.

    Leave a comment:


  • damiankao
    replied
    It looks like the gtf_to_sam script is not working. Do you have it in your path? Have you tried merging only the cufflinks gtf outputs together? Maybe the USCS gtf is not formatted in a way that cuffmerge can read? You can try running gtf_to_sam on a gtf file without cuffmerge and see if that works.

    Leave a comment:

Latest Articles

Collapse

  • seqadmin
    Non-Coding RNA Research and Technologies
    by seqadmin




    Non-coding RNAs (ncRNAs) do not code for proteins but play important roles in numerous cellular processes including gene silencing, developmental pathways, and more. There are numerous types including microRNA (miRNA), long ncRNA (lncRNA), circular RNA (circRNA), and more. In this article, we discuss innovative ncRNA research and explore recent technological advancements that improve the study of ncRNAs.

    Nobel Prize for MicroRNA Discovery
    This week,...
    10-07-2024, 08:07 AM
  • seqadmin
    Recent Developments in Metagenomics
    by seqadmin





    Metagenomics has improved the way researchers study microorganisms across diverse environments. Historically, studying microorganisms relied on culturing them in the lab, a method that limits the investigation of many species since most are unculturable1. Metagenomics overcomes these issues by allowing the study of microorganisms regardless of their ability to be cultured or the environments they inhabit. Over time, the field has evolved, especially with the advent...
    09-23-2024, 06:35 AM

ad_right_rmr

Collapse

News

Collapse

Topics Statistics Last Post
Started by seqadmin, 10-11-2024, 06:55 AM
0 responses
11 views
0 likes
Last Post seqadmin  
Started by seqadmin, 10-02-2024, 04:51 AM
0 responses
110 views
0 likes
Last Post seqadmin  
Started by seqadmin, 10-01-2024, 07:10 AM
0 responses
114 views
0 likes
Last Post seqadmin  
Started by seqadmin, 09-30-2024, 08:33 AM
1 response
121 views
0 likes
Last Post EmiTom
by EmiTom
 
Working...
X