Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • phageman
    Junior Member
    • Nov 2008
    • 2

    Viewing paired-end inconsistencies in 454 scaffolds

    Greetings
    We are attempting to sequence microbial genomes with paired-end 454 data supplemented with Illumina/Solexa GAII data to resolve homopolymers etc. Newbler assembly of the 454 data has generated some very nice scaffolds but I have detected at least one inverted contig. I was wondering if anybody knows a means of viewing the Newbler output that will show the paired end relationships as a means of detecting those that are inconsistent. It seems to me that the ACE file does not include scaffold information and Newbler generated scaffolds are simple multifasta files. Any assistance would be most appreciated.

    Cheers and thanks
  • andpet
    Member
    • Jul 2008
    • 27

    #2
    Viewing paired-end inconsistencies in 454 scaffolds

    Hi,

    have a look at the AMOS assembly package (http://amos.sourceforge.net/). It contains a script called amosvalidate that checks for such inconsistencies in assemblies
    (also described in this paper http://www.ncbi.nlm.nih.gov/sites/en...earch=18341692).

    The package also contains Hawkeye, a nice assembly viewer, that can visualize these inconsistencies and that is fast enough for displaying next generation sequencing data (at least for small assemblies).

    However installation of the amos package is a little bit tricky ...

    Greets,

    Andreas

    Comment

    • hlu
      Member
      • Jan 2009
      • 32

      #3
      Originally posted by phageman View Post
      Greetings
      We are attempting to sequence microbial genomes with paired-end 454 data supplemented with Illumina/Solexa GAII data to resolve homopolymers etc. Newbler assembly of the 454 data has generated some very nice scaffolds but I have detected at least one inverted contig. I was wondering if anybody knows a means of viewing the Newbler output that will show the paired end relationships as a means of detecting those that are inconsistent. It seems to me that the ACE file does not include scaffold information and Newbler generated scaffolds are simple multifasta files. Any assistance would be most appreciated.

      Cheers and thanks

      Have you looked at the newbler outout file "454PairStatus.txt"?
      This file prints all the pair reads status and coordinates for the assembly. It does not have all the nice pair info on ace file, but at lease it gives pair information there.

      Comment

      Latest Articles

      Collapse

      • SEQadmin2
        Nine Things a Sample Prep Scientist Thinks About Before Sequencing
        by SEQadmin2


        I’m not a sequencing expert. I’m a purification scientist who uses NGS to evaluate workflows my group develops. With this perspective, we think about the sample first and the NGS workflow second. The sequencer is an exceptionally honest reporter, but it can only report on what you give it, so whether you get clean, interpretable data from an NGS workflow is largely determined before you begin.


        Here are nine questions we think about, in roughly the order they matter, before...
        06-18-2026, 07:11 AM
      • SEQadmin2
        From Collection to Sequencing: Why Sample Preparation and Preservation Define Sequencing Data
        by SEQadmin2


        Data variability is still an issue in sequencing technologies despite the advances in reproducibility and accuracy of these platforms. But the problem does not originate in the sequencing itself, but in the previous steps, before the sample reaches the sequencer.


        The first step is collection, followed by preservation and sample preparation for analysis. Most scientists overlook those steps, but not being careful might just be skewing the experiment’s results.
        ...
        06-02-2026, 10:05 AM
      • SEQadmin2
        Single-Cell Sequencing at an Inflection Point: Early Impacts of New Platforms and Emerging Trends
        by SEQadmin2


        With the launch of new single-cell sequencing platforms in 2026, the field stands at an exciting inflection point. This article surveys the most impactful advances in the field and discusses how they’re reshaping research in cancer, immunology, and beyond.


        Introduction

        Single-cell sequencing technologies have undergone remarkable advances over the past decade, transitioning from low-throughput experimental approaches to highly scalable platforms capable of...
        05-22-2026, 06:42 AM

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by SEQadmin2, 06-17-2026, 06:09 AM
      0 responses
      21 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 06-09-2026, 11:58 AM
      0 responses
      38 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 06-05-2026, 10:09 AM
      0 responses
      45 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 06-04-2026, 08:59 AM
      0 responses
      49 views
      0 reactions
      Last Post SEQadmin2  
      Working...