Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • bfast match problem on fedora 14

    Hi everybody,

    I cant make bfast work on Fedora 14.
    I'm using unpaired SOLID data of 50 bp length.
    In version 0.6.4e, the solid2fastq step did not work properly for me. In the last version (0.6.4f git:50fb580ff23fe839b72b49924908159bd35d6f86) from the git repository, the bfast match step fails with the following error message:

    ...
    In total read 1 contigs for a total of 3171952 bases
    ************************************************************
    Reading /home/user/work/analysis/reads.1.fastq into a temp file.
    bfast: ../bfast/RGMatch.c:155: RGMatchPrint: Assertion `m->readLength > 0' failed.

    The performed steps were:
    1) solid2fastq -n 10000000 -o reads datafile.csfasta datafile.qual
    2) ~/tools/bfast/bfast/bfast fasta2brg -f refGenome.fna
    ~/tools/bfast/bfast/bfast fasta2brg -f refGenome.fna -A 1
    3) bfast index -f refGenome.fna -m 11111... -w 14 -i 1 -A 1 -n 8
    4) bfast match -f refGenome.fna -A 1 -r reads1.fastq -n 8 > tmp.bmf

    I want to try it on a virtual machine running Fedora 13. Would be happy about any further suggestions... Thanks in advance!

  • #2
    Looks like a read with zero bases, could you check for that in your fastq file?

    Originally posted by sammy07 View Post
    Hi everybody,

    I cant make bfast work on Fedora 14.
    I'm using unpaired SOLID data of 50 bp length.
    In version 0.6.4e, the solid2fastq step did not work properly for me. In the last version (0.6.4f git:50fb580ff23fe839b72b49924908159bd35d6f86) from the git repository, the bfast match step fails with the following error message:

    ...
    In total read 1 contigs for a total of 3171952 bases
    ************************************************************
    Reading /home/user/work/analysis/reads.1.fastq into a temp file.
    bfast: ../bfast/RGMatch.c:155: RGMatchPrint: Assertion `m->readLength > 0' failed.

    The performed steps were:
    1) solid2fastq -n 10000000 -o reads datafile.csfasta datafile.qual
    2) ~/tools/bfast/bfast/bfast fasta2brg -f refGenome.fna
    ~/tools/bfast/bfast/bfast fasta2brg -f refGenome.fna -A 1
    3) bfast index -f refGenome.fna -m 11111... -w 14 -i 1 -A 1 -n 8
    4) bfast match -f refGenome.fna -A 1 -r reads1.fastq -n 8 > tmp.bmf

    I want to try it on a virtual machine running Fedora 13. Would be happy about any further suggestions... Thanks in advance!

    Comment


    • #3
      Hi Nils,

      you are right, this seems to be a problem with the data integrity. The problem looked like that:

      @160_774_71
      T022221123122231102
      +
      BBBBBBABBABBABBBBABB+'))?@;55<<6@/);/1<5?91)-/5@9+

      If these four lines are removed from the file, it works. Thank you!

      Comment


      • #4
        If you run the "solid2fastq" step again, do you get the same problem read? Could you pull out the same read in the CSFAST/QUAL files so I can see what is going on?

        Comment


        • #5
          Ok, it seems that one pair of my .csfasta / .qual files was broken. Both just stop in the middle of a line without a newline character, which produces the short read in the solid2fastq output.

          Another strange thing is that the .csfasta and the corresponding .qual file even have a different number of entries (the .qual file is longer), and solid2fastq did not produce any error message concerning this; possibly it just discarded the rest.

          Comment


          • #6
            Sounds like your .csfasta / .qual files are corrupt. They should (IRC) have the same # of lines. It might be a good time to call up some support,

            Nils

            Comment

            Latest Articles

            Collapse

            • seqadmin
              Recent Advances in Sequencing Analysis Tools
              by seqadmin


              The sequencing world is rapidly changing due to declining costs, enhanced accuracies, and the advent of newer, cutting-edge instruments. Equally important to these developments are improvements in sequencing analysis, a process that converts vast amounts of raw data into a comprehensible and meaningful form. This complex task requires expertise and the right analysis tools. In this article, we highlight the progress and innovation in sequencing analysis by reviewing several of the...
              Yesterday, 07:48 AM
            • seqadmin
              Essential Discoveries and Tools in Epitranscriptomics
              by seqadmin




              The field of epigenetics has traditionally concentrated more on DNA and how changes like methylation and phosphorylation of histones impact gene expression and regulation. However, our increased understanding of RNA modifications and their importance in cellular processes has led to a rise in epitranscriptomics research. “Epitranscriptomics brings together the concepts of epigenetics and gene expression,” explained Adrien Leger, PhD, Principal Research Scientist...
              04-22-2024, 07:01 AM

            ad_right_rmr

            Collapse

            News

            Collapse

            Topics Statistics Last Post
            Started by seqadmin, Today, 06:57 AM
            0 responses
            9 views
            0 likes
            Last Post seqadmin  
            Started by seqadmin, Yesterday, 07:17 AM
            0 responses
            14 views
            0 likes
            Last Post seqadmin  
            Started by seqadmin, 05-02-2024, 08:06 AM
            0 responses
            19 views
            0 likes
            Last Post seqadmin  
            Started by seqadmin, 04-30-2024, 12:17 PM
            0 responses
            23 views
            0 likes
            Last Post seqadmin  
            Working...
            X