Seqanswers Leaderboard Ad

Collapse

Announcement

Collapse
No announcement yet.
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • Merging Assemblies with Minimus2

    I am trying to use Minimus2 to merge abyss assemblies. I also want to use it to run my assemblies against some 454 reads to try and get better value from these longer reads. I managed to get it working with a smaller test set but having difficulty with larger concatenated files from the assemblies.

    Is there a limit to the size of the input data that can be handled by miniums2?

    I am considering chopping up my assemblies into smaller faster files. I can then merge each file with the 454 data in turn. I could then use a clustering tool (CD-HIT-EST) to merge all the files to remove redundancy. Has anyone any experience/recommendations doing something like this?

  • #2
    Here is one of the problems I am having, when I concatenate two files from an abyss assembly (.fa files) and convert to afg (with toAmos) for use in minimus2 I get the following error.

    AFG ERROR: Sequence and quality lengths disagree
    could not parse 'RED' message with iid:1, message ignored
    ERROR: Sequence and quality lengths disagree
    could not parse 'RED' message with iid:2, message ignored
    ERROR: Sequence and quality lengths disagree
    could not parse 'RED' message with iid:3, message ignored
    ERROR: Sequence and quality lengths disagree
    could not parse 'RED' message with iid:4, message ignored
    and so on for all entries......

    I am at a bit of a loss to what is going on.... I don't have quality scores.

    here is what fasta file looks like:
    >3520 2510 57729
    ATATCTCATTTAGCTTCATTTGTATAACATCTGAAAACAAAAGTTAATCTCCACAGTCACAAGATAGCACTGAATTAGGT
    TCATACACAGAGGAAGCTAGAAATTGCAGATTGGTTCCGCGCTCCAAGTTTTTTAAAAATGATGCTTAAATACTACCTGA
    TACTCTAATCTTTGATGTAATACATGAAGGGAATAAGAAAAACACTTCATACCATGAGTTCATAGTGGTCCCTCACGCTG
    CACTTGTCCCTCACGGATACGTCAAA
    Last edited by SLB; 05-19-2011, 06:21 AM.

    Comment


    • #3
      toAmos error

      Originally posted by SLB View Post
      Here is one of the problems I am having, when I concatenate two files from an abyss assembly (.fa files) and convert to afg (with toAmos) for use in minimus2 I get the following error.

      AFG ERROR: Sequence and quality lengths disagree
      could not parse 'RED' message with iid:1, message ignored
      ERROR: Sequence and quality lengths disagree
      could not parse 'RED' message with iid:2, message ignored
      ERROR: Sequence and quality lengths disagree
      could not parse 'RED' message with iid:3, message ignored
      ERROR: Sequence and quality lengths disagree
      could not parse 'RED' message with iid:4, message ignored
      and so on for all entries......

      I am at a bit of a loss to what is going on.... I don't have quality scores.

      here is what fasta file looks like:
      >3520 2510 57729
      ATATCTCATTTAGCTTCATTTGTATAACATCTGAAAACAAAAGTTAATCTCCACAGTCACAAGATAGCACTGAATTAGGT
      TCATACACAGAGGAAGCTAGAAATTGCAGATTGGTTCCGCGCTCCAAGTTTTTTAAAAATGATGCTTAAATACTACCTGA
      TACTCTAATCTTTGATGTAATACATGAAGGGAATAAGAAAAACACTTCATACCATGAGTTCATAGTGGTCCCTCACGCTG
      CACTTGTCCCTCACGGATACGTCAAA

      Hi SLB,

      Were you able to figure it out? I am having the same error trying to combine abyss output. I am following this protocol: http://ged.msu.edu/angus/metag-assem...et-multik.html

      Please let me know if you were able to fix the problem.


      Thank you,

      -Milo

      Comment

      Latest Articles

      Collapse

      • seqadmin
        Recent Advances in Sequencing Analysis Tools
        by seqadmin


        The sequencing world is rapidly changing due to declining costs, enhanced accuracies, and the advent of newer, cutting-edge instruments. Equally important to these developments are improvements in sequencing analysis, a process that converts vast amounts of raw data into a comprehensible and meaningful form. This complex task requires expertise and the right analysis tools. In this article, we highlight the progress and innovation in sequencing analysis by reviewing several of the...
        05-06-2024, 07:48 AM
      • seqadmin
        Essential Discoveries and Tools in Epitranscriptomics
        by seqadmin




        The field of epigenetics has traditionally concentrated more on DNA and how changes like methylation and phosphorylation of histones impact gene expression and regulation. However, our increased understanding of RNA modifications and their importance in cellular processes has led to a rise in epitranscriptomics research. “Epitranscriptomics brings together the concepts of epigenetics and gene expression,” explained Adrien Leger, PhD, Principal Research Scientist...
        04-22-2024, 07:01 AM

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by seqadmin, 05-10-2024, 06:35 AM
      0 responses
      20 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 05-09-2024, 02:46 PM
      0 responses
      26 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 05-07-2024, 06:57 AM
      0 responses
      21 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 05-06-2024, 07:17 AM
      0 responses
      21 views
      0 likes
      Last Post seqadmin  
      Working...
      X