Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • ljhwahaha
    Junior Member
    • Oct 2010
    • 3

    #1

    Need some suggestion for overlap assembler

    Recently, i faced with a problem, I want to overlap the sequences in order to have a longer one, but i can't find out a assembler which could be suitable to my data.
    The length of my data is wide range, from 102bp to 87249bp, with N50 length of 738bp, so it count not be assembled using 454 data assembler, such as Newbler.
    What's more, the total bases number of my data is about 1.9G, so it seems to be impossible to use Sanger data assembler.
    What i want to do is to extend the sequences based on the overlap relationship between them, if someone have any suggestion, please inform me.
    thank you
  • niazi84@hotmail.com
    Member
    • Jan 2010
    • 25

    #2
    hello,

    I also want to do the same but could not find any software. Did you find any overlaping assembler?
    ~Adnan~

    Comment

    • sklages
      Senior Member
      • May 2008
      • 628

      #3
      Have a look at Celera Assembler, http://sourceforge.net/apps/mediawik...itle=Main_Page

      Comment

      • amaurizio
        Junior Member
        • Sep 2012
        • 4

        #4
        Hello,
        I used Pear to merge my Illumina (MiSeq sequencer) pair-end reads.
        I'd like to know the overlap length in each of the merged reads in order to calculate min length, max, average, mode, median etc...
        Can you suggest my how to do?
        I tried with a perl script (length R1 + length R2 - length MergedR1R2) but I am not very good in programming....
        Can anybody help me and tell me how to do this?
        Thanks!!

        Comment

        • krobison
          Senior Member
          • Nov 2007
          • 734

          #5
          Code:
          #!/usr/bin/perl
          #!/usr/bin/perl
          # debugging left as exercise for student :-)
          use strict;
          
          foreach my $arg(@ARGV)
          {
             my %lengths=();
             # read sequence file for lengths
             my $rdr=new Bio::SeqIO(-file=>$arg,-format=>'fastq');
             my $sum=0; my $cnt=0;
             while (my $rec=$rdr->next_seq)
             {
                $lengths{$rec->length}++; $sum+=$rec->length; $cnt++;
             }
             my @sortedLengths=sort {$a<=>$b} keys %lengths;
             my $minLen=$sortedLengths[0];
             my $maxLen=$sortedLengths[$#sortedLengths];
             my $meanLen=$sum/$cnt;
             my ($modeLen)=sort {$lengths{$b}<=>$lengths{$a}} keys %lengths;
          
             my $medLen="error";
             # calculating median left as exercise
          
             print join("\t",$arg,$minLen,$maxLen,$meanLen,$modeLen,$medLen),"\n";
          }

          Comment

          • amaurizio
            Junior Member
            • Sep 2012
            • 4

            #6
            Thank you very much!

            Comment

            Latest Articles

            Collapse

            • 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
              ...
              Today, 09:55 AM
            • SEQadmin2
              New Genomics Technologies Take Aim at Long-Standing Limits
              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
              ...
              09-28-2026, 10:25 AM

            ad_right_rmr

            Collapse

            News

            Collapse

            Topics Statistics Last Post
            Started by SEQadmin2, Today, 05:39 AM
            0 responses
            9 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, Yesterday, 09:56 AM
            0 responses
            11 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 10-09-2026, 11:14 AM
            0 responses
            25 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 09-29-2026, 09:51 AM
            0 responses
            76 views
            0 reactions
            Last Post SEQadmin2  
            Working...