Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • bioman1
    Member
    • May 2012
    • 80

    #1

    Mitobim-Any one used?- iteration problem

    I am trying to use MITObim for mitchondrial genome assembly project. I have tried tutorial provided in MITObim:https://github.com/chrishah/MITObim

    I have installed Mira 3.4.1.1 and MITObim 1.6. Mapping assembly with MIRA 3.4.1.1 was sucessful, however wrapper script MITObim 1.6 stops at iteration 1, it should iterate upto 8 according the the tutorial, it says error "mirabait seems to have failed". What will be the reason

    mapping assembly with MIRA 3.4.1.1:
    mira --project=initial-mapping-testpool-to-Salpinus-mt --job=mapping,genome,accurate,solexa -MI:somrnl=0 -AS:nop=1 -SB:bft=fasta:bbq=30:bsn=Salpinus-mt-genome SOLEXA_SETTINGS -CO:msr=no -SB:dsn=testpool

    for MITObim 1.6:
    MITObim.pl -start 1 -end 10 -strain testpool -ref Salpinus_mt_genome -readpool initial-mapping-testpool-to-Salpinus-mt_in.solexa.fastq -maf initial-mapping-testpool-to-Salpinus-mt_assembly/initial-mapping-testpool-to-Salpinus-mt_d_results/initial-mapping-testpool-to-Salpinus-mt_out.maf &> log

    below is the log file:

    MITObim - mitochondrial baiting and iterative mapping
    version 1.6
    author: Christoph Hahn, (c) 2012-2013


    Full command run: ../MITObim_1.6.pl -start 1 -end 10 -strain testpool -ref Salpinus_mt_genome -readpool initial-mapping-testpool-to-Salpinus-mt_in.solexa.fastq -maf initial-mapping-testpool-to-Salpinus-mt_assembly/initial-mapping-testpool-to-Salpinus-mt_d_results/initial-mapping-testpool-to-Salpinus-mt_out.maf

    All paramters seem to make sense:
    startiteration: 1
    enditeration: 10
    strainname: testpool
    refname: Salpinus_mt_genome
    readpool: /PATH/MITObim-master/testdata1/initial-mapping-testpool-to-Salpinus-mt_in.solexa.fastq
    maf: /PATH/Downloads/MITObim-master/testdata1/initial-mapping-testpool-to-Salpinus-mt_assembly/initial-mapping-testpool-to-Salpinus-mt_d_results/initial-mapping-testpool-to-Salpinus-mt_out.maf
    quick: 0
    paired: 0
    denovo: 0 (mapping=0, denovo=1)
    noshow: 0
    read trimming: 0 (off=0, on=1)
    kmer baiting: 31
    platform: SOLEXA
    clean: 0 (off=0, on=1)
    proofread: 0

    Starting MITObim

    ==============
    ITERATION 1
    ==============
    May 8 10:20:53


    recover backbone by running convert_project on maf file


    Parsing special MIRA parameters: SOLEXA_SETTINGS -CO:fnicpst=yes

    Ok.
    Loading from maf, saving to: fasta fastaqual
    First counting reads:
    [0%] ....|.... [10%] ....|.... [20%] ....|.... [30%] ....|.... [40%] ....|.... [50%] ....|.... [60%] ....|.... [70%] ....|.... [80%] ....|.... [90%] ....|.... [100%]
    Now loading and processing data:
    [0%] ....|.... [10%] ....|.... [20%] ....|.... [30%] ....|.... [40%] ....|.... [50%] ....|.... [60%] ....|.... [70%] ....|.... [80%] ....|.... [90%] ....|.Localtime: Thu May 8 10:20:53 2014

    Generated 1692 unique template ids for 2548 valid reads.
    Localtime: Thu May 8 10:20:53 2014

    Seeing strain 1: "testpool"
    Seeing strain 2: "Salpinus-mt-genome"
    Generated 2 unique strain ids for 2548 reads.
    makeIntelligentConsensus() complete calc
    makeIntelligentConsensus() complete calc
    makeIntelligentConsensus() complete calc
    makeIntelligentConsensus() complete calc
    makeIntelligentConsensus() complete calc
    makeIntelligentConsensus() complete calc
    makeIntelligentConsensus() complete calc
    makeIntelligentConsensus() complete calc
    makeIntelligentConsensus() complete calc
    makeIntelligentConsensus() complete calc
    makeIntelligentConsensus() complete calc
    makeIntelligentConsensus() complete calc
    ... [100%]

    Data conversion process finished, no obvious errors encountered.
    SC Read:: read name issorted (1) capacity 4294967295(4) size 1
    SC Read:: scf path name issorted (1) capacity 255(1) size 1
    SC Read:: exp path name issorted (1) capacity 255(1) size 1
    SC Read:: machine type issorted (1) capacity 255(1) size 1
    SC Read:: primer issorted (1) capacity 255(1) size 1
    SC Read:: strain issorted (1) capacity 255(1) size 3
    SC Read:: base caller issorted (1) capacity 255(1) size 1
    SC Read:: dye issorted (1) capacity 255(1) size 1
    SC Read:: process status issorted (1) capacity 255(1) size 1
    SC Read:: clone vector name issorted (1) capacity 65535(2) size 1
    SC Read:: sequencing vector name issorted (1) capacity 65535(2) size 1
    SC asped issorted (1) capacity 4294967295(4) size 1


    fishing readpool using mirabait (k = 31)



    mirabait seems to have failed - see detailed output above
  • maubp
    Peter (Biopython etc)
    • Jul 2009
    • 1544

    #2
    See also this thread: http://seqanswers.com/forums/showthread.php?t=43064

    I suggest you email the authors or the mira_talk mailing list, and include links to these threads.

    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, Yesterday, 11:13 AM
    0 responses
    16 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, Yesterday, 10:48 AM
    0 responses
    15 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 10-15-2026, 10:52 AM
    0 responses
    35 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...