Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts

  • Nino
    replied
    @crazyhottommy

    Try this script. It gives you the fastq file instead of the sam/bam file

    #!/usr/bin/perl -w

    use warnings;
    use strict;

    my $datafile = $ARGV[0];
    my $outfile = $ARGV[1];

    open (IN, $datafile) or die "can't open the datafile: $datafile\n";
    open (OUT, ">$outfile") or die "can't open the outputfile: $outfile\n";

    while(my $line=<IN>){
    chomp $line;
    my @i = split(/\t/, $line);
    print OUT "@".$i[0].":".$i[1].$i[2].":".$i[3].":".$i[4].":".$i[5]."#".$i[6]."/".$i[7]."\n".$i[8]."\n"."+"."\n".$i[9]."\n";
    }
    close IN;
    close OUT;

    Leave a comment:


  • crazyhottommy
    replied
    Originally posted by GenoMax View Post
    @crazyhottommy: You should clarify on your blog post that your modifications are specifically targeted for human (?) data. If someone else has a different genome it would be incorrect to follow your procedure, as is.

    @Nino/@crazyhottommy: I am not sure what the downstream application is/was in your case but you have to account for the Q-scores probably being in non-sanger format (this is old data). Most new tools will expect them to be in sanger format.

    @Nino: Check your PM. I sent you a script to recreate fastq sequence file yesterday. That may be a safer place to start. I can post it here if it works for you.
    Thanks, I updated the post accordingly.

    Leave a comment:


  • Nino
    replied
    @GenoMax: I received your PM if you could please look at my response to see if the file I am working on is an alignment file. Also the data I am working with is from NCBI website which I downloaded to use, apparently they (people who uploaded the data) used the CASAVA Illumina pipeline (this is all the information that was given to me).

    Leave a comment:


  • GenoMax
    replied
    @crazyhottommy: You should clarify on your blog post that your modifications are specifically targeted for human (?) data. If someone else has a different genome it would be incorrect to follow your procedure, as is.

    @Nino/@crazyhottommy: I am not sure what the downstream application is/was in your case but you have to account for the Q-scores probably being in non-sanger format (this is old data). Most new tools will expect them to be in sanger format.

    @Nino: Check your PM. I sent you a script to recreate fastq sequence file yesterday. That may be a safer place to start. I can post it here if it works for you.

    Leave a comment:


  • crazyhottommy
    replied
    Originally posted by Nino View Post
    Hey were you ever able to find a solution to your problem? I am currently running into the same issue as well.

    [jhpce01 /amber3/feinbergLab/personal/sramazan/chip-seq]$ /amber3/feinbergLab/personal/sramazan/perl/scripts/export2sam.pl --read1=GSM1053091_mm9.nac.inp1.sorted.txt
    @PG ID:export2sam.pl VN:2.3.1 CL:/amber3/feinbergLab/personal/sramazan/perl/scripts/export2sam.pl --read1=GSM1053091_mm9.nac.inp1.sorted.txt

    ERROR: Unexpected number of fields in export record on line 1 of read1 export file. Found 16 fields but expected 22.
    ...erroneous export record:
    HWI-EASXXX 1 2 35 1301 1347 0 1 ATGTAGCTAGAGACTTGAGCTCTGGGGGGTACTGGT aaa^]`aa`a_a_[_^`^`__`^^^][_XLQR[[]S chr10.fa 3003189 F 36 12
    see my post here http://crazyhottommy.blogspot.com/20...-bam-file.html

    Leave a comment:


  • Nino
    replied
    Hey were you ever able to find a solution to your problem? I am currently running into the same issue as well.

    [jhpce01 /amber3/feinbergLab/personal/sramazan/chip-seq]$ /amber3/feinbergLab/personal/sramazan/perl/scripts/export2sam.pl --read1=GSM1053091_mm9.nac.inp1.sorted.txt
    @PG ID:export2sam.pl VN:2.3.1 CL:/amber3/feinbergLab/personal/sramazan/perl/scripts/export2sam.pl --read1=GSM1053091_mm9.nac.inp1.sorted.txt

    ERROR: Unexpected number of fields in export record on line 1 of read1 export file. Found 16 fields but expected 22.
    ...erroneous export record:
    HWI-EASXXX 1 2 35 1301 1347 0 1 ATGTAGCTAGAGACTTGAGCTCTGGGGGGTACTGGT aaa^]`aa`a_a_[_^`^`__`^^^][_XLQR[[]S chr10.fa 3003189 F 36 12

    Leave a comment:


  • crazyhottommy
    replied
    Hi all,

    I found http://genomewiki.ucsc.edu/index.php/ABRF2010_Tutorial

    I downloaded the latest version of samtools

    I use export2sam.pl --read1=chr21_export.txt \
    | perl -wpe 's/(chr.*)\.fa/$1/' \
    > chr21.sam

    it says

    ERROR: Unexpected number of fields in export record on line 1 of read1 export file. Found 16 fields but expected 22.

    my sorted.txt file only contains 16 fields, and the program is complaining about that.

    but the example file given in the link above also contains only 16 fields.
    I though may be they changed the format. so I then downloaded the earlier version of samtools (0.1.8,0.1.9 etc...)

    still, it gave me error like:

    Use of uninitialized value $t[21] in string eq at export2sam.pl line 279,


    earlier version just says die at liine 17.

    Can anyone help me? Thanks!

    Leave a comment:


  • how to convert sorted.txt files from the Illumina pipeline v1.3.4 to bam or sam?

    Hi all,

    how to convert the sorted.txt file from illumina pipeline to bam or sam file?

    Thanks.

Latest Articles

Collapse

  • SEQadmin2
    16S/ITS Profiling vs. Shotgun Metagenomics: What Changes in Your Workflow?
    by SEQadmin2




    NGS has revolutionized clinical microbiology by offering new ways to identify and surveil pathogens without prior knowledge of the target. One popular approach is 16S rRNA and ITS amplicon sequencing, which targets specific microbial markers. But studies are increasingly incorporating shotgun metagenomics, a technique that sequences all DNA from a sample without targeting specific microbial markers. This approach allows more detailed taxonomic classification, detection...
    Yesterday, 06:46 AM
  • SEQadmin2
    Multiomic Liquid Biopsy: What DNA/RNA Panels Reveal That DNA Alone Can’t
    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
    ...
    10-14-2026, 09:55 AM

ad_right_rmr

Collapse

News

Collapse

Topics Statistics Last Post
Started by SEQadmin2, 10-28-2026, 09:57 AM
0 responses
31 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 10-28-2026, 09:51 AM
0 responses
21 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 10-22-2026, 11:13 AM
0 responses
71 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 10-22-2026, 10:48 AM
0 responses
48 views
0 reactions
Last Post SEQadmin2  
Working...