Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • harrb
    Junior Member
    • Feb 2008
    • 5

    #1

    documentation for ABySS

    Hello,

    I am a new user of ABySS. I have 50 Million Solexa 100bp paired-end transcriptome reads that I am intending to assemble de novo. Velvet could not handle my dataset, but my first run with ABySS worked. However, I have a hard time understanding the output.
    I have 4 questions:

    1) I could not find any documentation on the output files created. Can someone maybe direct me to a page where the various files are explained?

    2) I also do not quite understand if ABySS considers the paired end reads for the alignment or not. Does someone know? I have run the "pe" mode.

    3) What is the number of mismatches allowed in a read to still be assembled to a contig?

    4) below I pasted a few contigs from the outfile that Abyss has created (i.e. xxx_contigs.fa)


    >29036 60 1326
    GGCTCGAGGGTATCTAGAGTCACCAAAGCTGCCGGGCGGGCCCGGGGTGGGTTTGGTCTG
    >29037 61 114
    CGGCTCGAGGGTATCTAGAGTCACCAAAGCTGCCGGGCGGGCCCGGGGTGGGTTTGGGTTG
    >29038 62 268
    TCGGCTCGAGGGTATCTAGAGTCACCAAAGCTGCCGGGCGGGCCCGGGGTGGGTTTGGTGTG
    >29039 60 1139
    GGCTCGAGGGTATCTAGAGTCACCAAAGCTGCCGGGCGGGCCCGGGGTGGGTTTGGGCTG
    >29040 61 51
    CGGCTCGAGGGTATCTAGAGTCACCAAAGCTGCCGGGCGGGCCCGGGGTGGGTTTGGGCCG
    >29041 60 13
    GGCTCGAGGGTATCTAGAGTCACCAAAGCTGCCGGGCGGGCCCGGGGTGGGTTTGGGCTT
    >29042 61 183
    CGGCTCGAGGGTATCTAGAGTCACCAAAGCTGCCGGGCGGGCCCGGGGTGGGTTTGGGGTG
    >29043 61 44
    CGGCTCGAGGGTATCTAGAGTCACCAAAGCTGCCGGGCGGGCCCGGGGTGGGTTTGGTCCG
    >29044 61 70
    CGGCTCGAGGGTATCTAGAGTCACCAAAGCTGCCGGGCGGGCCCGGGGTGGGTTTGGTTTG
    >29045 69 20
    GGCTCGAGGGTATCTAGAGTCACCAAAGCTGCCGGGCGGGCCCGGGGTGGGTTTGGGCTCATAAATGCA
    >29046 69 34
    GGCTCGAGGGTATCTAGAGTCACCAAAGCTGCCGGGCGGGCCCGGGGTGGGTTTGGTCTCATAAATGCA
    >29047 69 20
    GGCTCGAGGGTATCTAGAGTCACCAAAGCTGCCGGGCGGGCCCGGGGTGGGTTTGGTCTTGTAAATGCA

    It is quite clear that these reads are identical with the exception of a few single base mismatchs. Why are they not merged into a single contig?

    Thanks so much for your help!
    Last edited by harrb; 11-23-2010, 08:58 AM.
  • Bioinfo
    Member
    • Jul 2010
    • 15

    #2
    Originally posted by harrb View Post
    Hello,

    I am a new user of ABySS. I have 50 Million Solexa 100bp paired-end transcriptome reads that I am intending to assemble de novo. Velvet could not handle my dataset, but my first run with ABySS worked. However, I have a hard time understanding the output.
    I have 4 questions:

    1) I could not find any documentation on the output files created. Can someone maybe direct me to a page where the various files are explained?

    2) I also do not quite understand if ABySS considers the paired end reads for the alignment or not. Does someone know? I have run the "pe" mode.

    3) What is the number of mismatches allowed in a read to still be assembled to a contig?

    4) below I pasted a few contigs from the outfile that Abyss has created (i.e. xxx_contigs.fa)


    >29036 60 1326
    GGCTCGAGGGTATCTAGAGTCACCAAAGCTGCCGGGCGGGCCCGGGGTGGGTTTGGTCTG
    >29037 61 114
    CGGCTCGAGGGTATCTAGAGTCACCAAAGCTGCCGGGCGGGCCCGGGGTGGGTTTGGGTTG
    >29038 62 268
    TCGGCTCGAGGGTATCTAGAGTCACCAAAGCTGCCGGGCGGGCCCGGGGTGGGTTTGGTGTG
    >29039 60 1139
    GGCTCGAGGGTATCTAGAGTCACCAAAGCTGCCGGGCGGGCCCGGGGTGGGTTTGGGCTG
    >29040 61 51
    CGGCTCGAGGGTATCTAGAGTCACCAAAGCTGCCGGGCGGGCCCGGGGTGGGTTTGGGCCG
    >29041 60 13
    GGCTCGAGGGTATCTAGAGTCACCAAAGCTGCCGGGCGGGCCCGGGGTGGGTTTGGGCTT
    >29042 61 183
    CGGCTCGAGGGTATCTAGAGTCACCAAAGCTGCCGGGCGGGCCCGGGGTGGGTTTGGGGTG
    >29043 61 44
    CGGCTCGAGGGTATCTAGAGTCACCAAAGCTGCCGGGCGGGCCCGGGGTGGGTTTGGTCCG
    >29044 61 70
    CGGCTCGAGGGTATCTAGAGTCACCAAAGCTGCCGGGCGGGCCCGGGGTGGGTTTGGTTTG
    >29045 69 20
    GGCTCGAGGGTATCTAGAGTCACCAAAGCTGCCGGGCGGGCCCGGGGTGGGTTTGGGCTCATAAATGCA
    >29046 69 34
    GGCTCGAGGGTATCTAGAGTCACCAAAGCTGCCGGGCGGGCCCGGGGTGGGTTTGGTCTCATAAATGCA
    >29047 69 20
    GGCTCGAGGGTATCTAGAGTCACCAAAGCTGCCGGGCGGGCCCGGGGTGGGTTTGGTCTTGTAAATGCA

    It is quite clear that these reads are identical with the exception of a few single base mismatchs. Why are they not merged into a single contig?

    Thanks so much for your help!
    Hi,
    hope this paper may helps you..
    best
    Attached Files

    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
      ...
      10-14-2026, 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, 10-22-2026, 11:13 AM
    0 responses
    23 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 10-22-2026, 10:48 AM
    0 responses
    20 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 10-15-2026, 10:52 AM
    0 responses
    36 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 10-14-2026, 05:39 AM
    0 responses
    42 views
    0 reactions
    Last Post SEQadmin2  
    Working...