Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • rivabros
    Junior Member
    • Feb 2011
    • 6

    #1

    Trouble with box-plot of quality data in SOLID

    hi everyone,
    I have used the SOLiD2std.pl to change the csfasta and qual files to standard fastq files.
    I then ran fastqc to view boxplots of quality data and got these results, attached.
    They seem to have poor quality every 5 nt, as if the primer 5 of the procedure failed....
    Has anyone seen this type of quality plots before???
    I am new with solid data, have worked with ilumina and 454 before.
    Thanks for any guidance in advance.
    cheers
    maximo
    Attached Files
  • Jean
    Member
    • Nov 2008
    • 37

    #2
    You can not convert colorspace to basespace directly. See here why:
    Discussion of next-gen sequencing related bioinformatics: resources, algorithms, open source efforts, etc

    Comment

    • colindaven
      Senior Member
      • Oct 2008
      • 417

      #3
      An alternative route to using FastQC, which is very nice, is to align first and use the resulting BAM file as input.

      Another program I have looked at for duplicate analysis is prinseq, which also offers graphical output.

      Comment

      • Krish_143
        Member
        • Jan 2012
        • 45

        #4
        Did you removed adapter info or trimmed your reads.
        what about other fastQC results they are pass or fail.
        Krishna

        Comment

        • rivabros
          Junior Member
          • Feb 2011
          • 6

          #5
          Originally posted by Krish_143 View Post
          Did you removed adapter info or trimmed your reads.
          what about other fastQC results they are pass or fail.
          Some aspects passed and others failed,
          I did NO removal of adapters.... Not sure if it was done when i received the csfasta and qual files..
          Taking into consideration that this is a direct conversion from color to base space, its understandable that there may be confusing results.... (In all about 45% of reads mapped with color-space-novoAlign to a reference, and only 15% usnig colorspace-tophat/bowtie...)
          Any thoughts?
          PASS Basic Statistics Corrida_4_FC_1_01_01CVATFR001_F3.fastq
          FAIL Per base sequence quality Corrida_4_FC_1_01_01CVATFR001_F3.fastq
          WARN Per sequence quality scores Corrida_4_FC_1_01_01CVATFR001_F3.fastq
          WARN Per base sequence content Corrida_4_FC_1_01_01CVATFR001_F3.fastq
          FAIL Per base GC content Corrida_4_FC_1_01_01CVATFR001_F3.fastq
          FAIL Per sequence GC content Corrida_4_FC_1_01_01CVATFR001_F3.fastq
          WARN Per base N content Corrida_4_FC_1_01_01CVATFR001_F3.fastq
          PASS Sequence Length Distribution Corrida_4_FC_1_01_01CVATFR001_F3.fastq
          PASS Sequence Duplication Levels Corrida_4_FC_1_01_01CVATFR001_F3.fastq
          PASS Overrepresented sequences Corrida_4_FC_1_01_01CVATFR001_F3.fastq
          FAIL Kmer Content Corrida_4_FC_1_01_01CVATFR001_F3.fastq

          Comment

          • colindaven
            Senior Member
            • Oct 2008
            • 417

            #6
            I would recommend using SAET to clear up any colour errors before alignment. Normally I get 1-5% more aligned reads using this (apparently a lot more with ECC data).

            I don't think your fastqc boxplot results are too bad, but I've seen better ones.

            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
              ...
              Yesterday, 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, 10:52 AM
            0 responses
            8 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, Yesterday, 05:39 AM
            0 responses
            15 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 10-13-2026, 09:56 AM
            0 responses
            15 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 10-09-2026, 11:14 AM
            0 responses
            27 views
            0 reactions
            Last Post SEQadmin2  
            Working...