Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • maq pair end alignment error

    maq pair end alignment error

    maq map out.map re.bfa pair1.bfq pair2.bfq

    -- maq-0.6.3
    [ma_load_reads] loading reads...
    [ma_load_reads] set length of the first read as 41.
    [ma_load_reads] set length of the second read as 41.
    maq: read.cc:59: longreads_t* ma_load_reads(void*, int, void*, int): Assertion `strcmp(name, lr->name[j]) == 0' failed.
    Aborted


    what's the problem?

  • #2
    Any specific reason for using the much older 0.6.3? Sorry not sure of why the error though..
    --
    bioinfosm

    Comment


    • #3
      pair1.fq:
      @seq1_1
      CCCTAAACCCTAAACCCTAAACCCTAAACCTCTGAATCCTT
      +seq1_1
      hhYhhRhhhhhhhhfhh`ThhdhXTaVNWJLKGgcKGgcKG
      @seq2_1
      TAAACCCTAAACCTCTGAATCCTTAATCCCTAAATCCCTAA
      +seq2_1
      hhchh[h]hhhhhVhhhhLhdhhgPPhhUSYOOPQYOOPQQ
      @seq3_1
      AATCCTACATCCATGAATCCCTAAATACCTAATTCCCTAAA
      +seq3_1
      hhhhhhhhhhhhYPhhhhhKhhhTacNhhOF]IIDOF]IID

      pair2.fq:
      @seq1_2
      ACAAATCCTATTTCTTGTGGTTTTCTTTCCTTCACTTAGCT
      +seq1_2
      hhYhhRhhhhhhhhfhh`ThhdhXTaVNWJLKGgcKGgcKG
      @seq2_2
      GTTTTCTTTCCTTCACTTAGCTATGGATGGTTTATCTTCAT
      +seq2_2
      hhchh[h]hhhhhVhhhhLhdhhgPPhhUSYOOPQYOOPQQ
      @seq3_2
      CGAGCACACACACACGGTGGCTATCATCGATCGATCGATGC
      +seq3_2
      hhhhhhhhhhhhYPhhhhhKhhhTacNhhOF]IIDOF]IID

      maq-0.7.1/maq map out.map re.bfa pair1.bfq pair2.bfq

      results:
      seq1_1 ref 1 + 223 1 61 61 61 0 0 1 0
      41 CCCTAAACCCTAAACCCTAAACCCTAAACCTCTGAATCCTT ``Y``R````````````T````XT`VNWJLKG``KG``KG
      seq2_1 ref 18 + 225 1 61 61 61 0 0 1 0
      41 TAAACCCTAAACCTCTGAATCCTTAATCCCTAAATCCCTAA `````[`]`````V````L`````PP``USYOOPQYOOPQQ
      seq3_1 ref 66 + 0 64 61 61 0 0 0 1 0
      41 AATCCTACATCCATGAATCCCTAAATACCTAATTCCCTAAA ````````````YP`````K```T``N``OF]IIDOF]IID
      seq3_1 ref 66 + 0 192 0 0 0 0 0 0 0
      41 CGAGCACACACACACGGTGGCTATCATCGATCGATCGATGC ````````````YP`````K```T``N``OF]IIDOF]IID
      seq1_1 ref 223 + -223 1 61 61 61 0 0 1 0
      41 ACAAATCCTATTTCTTGTGGTTTTCTTTCCTTCACTTAGCT ``Y``R````````````T````XT`VNWJLKG``KG``KG
      seq2_1 ref 242 + -225 1 61 61 61 0 0 1 0
      41 GTTTTCTTTCCTTCACTTAGCTATGGATGGTTTATCTTCAT `````[`]`````V````L`````PP``USYOOPQYOOPQQ

      it's strange! the read id , the mapping position 66

      Comment


      • #4
        You should change your read name to:

        seq1/1, seq1/2
        seq2/1, seq2/2

        MAQ needs to parse the read names to get pairing. Sorry for the inconvenience.

        Comment


        • #5
          Thanks for your reply! Now I get new result:

          seq1/1 ref 1 + 164 1 61 61 61 0 0 1 0 35 C
          CCTAAACCCTAAACCCTAAACCCTAAACCTCTGA ``Y``R````````````T````XT`VNWJLKG``
          seq2/1 ref 40 + 208 1 61 61 61 0 0 1 0 35 T
          TAATCCCTAAATCCCTAAATCTTTAAATCCTACA `````[`]`````V````L`````PP``USYOOPQ
          seq3/1 ref 79 + 0 192 0 0 0 0 0 0 0 35 G
          GGGGGGGGGGGGGCCCCCCCCCCCCCCCCCCCCC ````````````YP`````K```T``N``OF]IID
          seq3/2 ref 79 + 0 64 61 61 0 0 0 1 0 35 T
          GAATCCCTAAATACCTAATTCCCTAAACCCGAAA `]`````V````L`````PP``USYOOPQYOOPQQ
          seq1/2 ref 164 + -164 1 61 61 61 0 0 1 0 35 T
          TTTATGTAATTGCTTATTGTTGTGTGTAGATTTT ````````````T````XT`VNWJLKG``KG``KG
          seq2/2 ref 247 + -208 1 61 61 61 0 0 1 0 35 C
          TTTCCTTCACTTAGCTATGGATGGTTTATCTTCA ````````````YP`````K```T``N``OF]IID

          seq3/2 align on postion 79 , seq3/1 could not aligned but Maq also display it.
          How Maq output pair read alignment?

          Comment

          Latest Articles

          Collapse

          • seqadmin
            Current Approaches to Protein Sequencing
            by seqadmin


            Proteins are often described as the workhorses of the cell, and identifying their sequences is key to understanding their role in biological processes and disease. Currently, the most common technique used to determine protein sequences is mass spectrometry. While still a valuable tool, mass spectrometry faces several limitations and requires a highly experienced scientist familiar with the equipment to operate it. Additionally, other proteomic methods, like affinity assays, are constrained...
            04-04-2024, 04:25 PM
          • seqadmin
            Strategies for Sequencing Challenging Samples
            by seqadmin


            Despite advancements in sequencing platforms and related sample preparation technologies, certain sample types continue to present significant challenges that can compromise sequencing results. Pedro Echave, Senior Manager of the Global Business Segment at Revvity, explained that the success of a sequencing experiment ultimately depends on the amount and integrity of the nucleic acid template (RNA or DNA) obtained from a sample. “The better the quality of the nucleic acid isolated...
            03-22-2024, 06:39 AM

          ad_right_rmr

          Collapse

          News

          Collapse

          Topics Statistics Last Post
          Started by seqadmin, 04-11-2024, 12:08 PM
          0 responses
          22 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-10-2024, 10:19 PM
          0 responses
          24 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-10-2024, 09:21 AM
          0 responses
          20 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-04-2024, 09:00 AM
          0 responses
          52 views
          0 likes
          Last Post seqadmin  
          Working...
          X