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  • rhinoceros
    replied
    Originally posted by luiscunhamx View Post
    Hi Amery, sorry just saw your question now, the good news is yes I solve it but the bad news is that the solution was running it with only one processor. I would love to know if you could also solve it by other way, because it takes ages running it with only one thread.

    Cheers

    L
    Just reporting the same problem with SSPACE_Standard_v3.0, but only when "-x 1". "-T 1" didn't fix it for me. Could the problem be in ExtendOrFormatContigs.pl if statements?

    Code:
    if($#filesbowtie >[B]=[/B] 0)
    ..
    if($#filesbwa >[B]=[/B] 0 || $#filesbwasw >[B]=[/B] 0){
    Shouldn't these be ">=1" or ">0"? The program finishes just fine if I use bwa or bwasw instead of bowtie..
    Last edited by rhinoceros; 05-29-2014, 09:32 PM.

    Leave a comment:


  • rotblaugelb
    replied
    hi boetsie,

    i just stumbled across your program and would like to use it.
    for the read libraries, how are they build? could you give an example of the steps to get there? i have read files in fastq format let's say R1.fastq and R2.fastq

    thanks, julia

    Leave a comment:


  • luiscunhamx
    replied
    Hi Amery, sorry just saw your question now, the good news is yes I solve it but the bad news is that the solution was running it with only one processor. I would love to know if you could also solve it by other way, because it takes ages running it with only one thread.

    Cheers

    L

    Leave a comment:


  • duxingxia
    replied
    Originally posted by luiscunhamx View Post
    Hi Boetsie

    Hi hope you can help me. I have been trying to use sspace to scaffold a old assembly with a new paired end library, several times, using different parameters and keeps giving the following error:
    "Thread 26 terminated abnormally: Can't open bwa output -- fatal"

    Although in my library file I have bowtie as selected aligner

    "lib1 bowtie ../corrected_trimmomatic_rubellus_1.fastq.gz ../corrected_trimmomatic_rubellus_2.fastq.gz 225 0.60 FR"

    The last log message is that is doing the mapping stage

    "2014: Mapping reads to contigs with Bowtie"

    and that's it,

    Can you please advise me where to look in order to try track the issue?

    Thanking in advance

    Luis
    I have same problem. Have you solved the problem, Luis?

    Amery

    Leave a comment:


  • luiscunhamx
    replied
    Hi Boetsie

    Hi hope you can help me. I have been trying to use sspace to scaffold a old assembly with a new paired end library, several times, using different parameters and keeps giving the following error:
    "Thread 26 terminated abnormally: Can't open bwa output -- fatal"

    Although in my library file I have bowtie as selected aligner

    "lib1 bowtie ../corrected_trimmomatic_rubellus_1.fastq.gz ../corrected_trimmomatic_rubellus_2.fastq.gz 225 0.60 FR"

    The last log message is that is doing the mapping stage

    "2014: Mapping reads to contigs with Bowtie"

    and that's it,

    Can you please advise me where to look in order to try track the issue?

    Thanking in advance

    Luis

    Leave a comment:


  • ret4andry
    replied
    I'd still like to use 454 PE data to scaffold my assembly. Is there some intermediate file or Bowtie like PE format that we can feed to SSPACE?

    Leave a comment:


  • condomitti
    replied
    Originally posted by boetsie View Post
    Sorry for the late reply. It seems that I do not get an e-mail notification anymore when a reply is given in this thread

    Please have a look at this post where colindaven suggests how to fix the problem;

    Discussion of next-gen sequencing related bioinformatics: resources, algorithms, open source efforts, etc


    Boetsie

    Thanks Boetsie! That seems to solve!!

    Cheers,
    Condomitti.

    Leave a comment:


  • boetsie
    replied
    Sorry for the late reply. It seems that I do not get an e-mail notification anymore when a reply is given in this thread

    Please have a look at this post where colindaven suggests how to fix the problem;

    Discussion of next-gen sequencing related bioinformatics: resources, algorithms, open source efforts, etc


    Boetsie

    Originally posted by condomitti View Post
    Hi Boetsie,

    Do you have a clue on how I could find out about that error?

    Thank you very much!

    Best rgrds,
    Conomitti.

    Leave a comment:


  • condomitti
    replied
    Hi Boetsie,

    Do you have a clue on how I could find out about that error?

    Thank you very much!

    Best rgrds,
    Conomitti.

    Leave a comment:


  • condomitti
    replied
    Hello fellows,

    I've been trying to assemble pre-assembled contigs into scaffolds using SSPACE. Everything goes ok up to a specific point where the software stops and gives me the following message:

    Bowtie-build error; -1 at /usr/local/src/sspace-basic/bin/PairingAndScaffolding.pl line 829.

    I tried running with -v option but no extra messages are output.
    Could please someone give me some help on how to debug that issue?

    I'm using a single fastq file of pre-assembled contigs and enabling contig extension ( -x 1 ) option, which should use a set of mate-pair reads I'm passing in on libraries.txt file.


    Thanks a lot.

    Cheers,
    George Condomitti.

    Leave a comment:


  • DAPOR
    replied
    Hi Anna,

    How did you solve the problem with "Can't locate getopts.pl in @INC (@INC contains"
    I can't figure it out

    Thanks

    Leave a comment:


  • maubp
    replied
    Originally posted by boetsie View Post
    yes, this is possible. The file should be in a TAB delimited format like:

    <contig1> <startpos_on_contig1> <endpos_on_contig1> <contig2> <startpos_on_contig2> <endpos_on_contig2>

    E.g.
    contig1 100 150 contig1 350 300
    contig1 4000 4050 contig2 110 60

    There is a script in the 'tools' directory of the package to convert SAM/BAM to a tab format.

    Regards,
    Boetsie
    Where should we report SSPACE bugs? The tools/sam_bam2Tab.pl script included in SSPACE basic v2.0 is extremely brittle - it cannot handle properly formatted paired end SAM/BAM (using the FLAG field), and instead expects fake single read data with read suffices (and only looks at the reverse complement bit of the FLAG). Thanks.

    Update: I've started hacking together a Python replacement https://github.com/peterjc/picobio/b..._sspace_tab.py
    Last edited by maubp; 02-20-2014, 02:54 AM. Reason: Adding link to alternative

    Leave a comment:


  • cronopio
    replied
    Hi Boetsie,

    I've tried to run the SSPACE example (E. Coli, contigs_abyss.fasta, etc.) in order to test the program.
    I follow all the steps, but the final result is a file with 111 scaffolds. Why is that? I was supposed to get only a few scaffolds, isn't?

    Could you please give me some advices? I don't know what I'm doing wrong.

    Thank you very much.
    Germán.

    Leave a comment:


  • xuseq
    replied
    Hi, Anna

    That's right! Thank you!


    Originally posted by OTU View Post
    Xu,

    Have you specified the output directory in your command line?
    If yes - delete it.

    Leave a comment:


  • OTU
    replied
    Xu,

    Have you specified the output directory in your command line?
    If yes - delete it.

    Leave a comment:

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