Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • tophat pair end reads

    I just finished mapping my ABI pair end colorspace reads with tophat. The reads were 50bp F3 and 25bp F5.

    When I tried to convert the .bam file into .sam for Cufflinks assembly using Picard Tools, I got this error:

    Exception in thread "main" java.lang.RuntimeException: SAM validation error: ERROR: Record 127338, Read name 507_970_1560_F3, Mate Alignment start (542169) must be <= reference sequence length (531507) on reference Contig1

    It looks like a read is being "mapped" outside of the reference contig?

    Bowtie has --fr, --rf, --ff options when aligning pair-end reads. Does tophat take into account that SOLiD mate pairs are both in forward direction? so the --ff would be used.
    Last edited by damiankao; 10-28-2010, 01:21 AM.

  • #2
    Originally posted by damiankao View Post
    I just finished mapping my ABI pair end colorspace reads with tophat. The reads were 50bp F3 and 25bp F5.

    When I tried to convert the .bam file into .sam for Cufflinks assembly using Picard Tools, I got this error:

    Exception in thread "main" java.lang.RuntimeException: SAM validation error: ERROR: Record 127338, Read name 507_970_1560_F3, Mate Alignment start (542169) must be <= reference sequence length (531507) on reference Contig1

    It looks like a read is being "mapped" outside of the reference contig?

    Bowtie has --fr, --rf, --ff options when aligning pair-end reads. Does tophat take into account that SOLiD mate pairs are both in forward direction? so the --ff would be used.

    TopHat maps left and right reads separately using Bowtie, that is, it doesn't use Bowtie's pair searching like --fr, --rf, --ff. Using the mapped reads, TopHat finds pairs if the two reads of a pair are on different strand (it ignores if they are on the same strand) and the inner distance is within user specified range.

    Comment


    • #3
      TopHat mapping outside reference contig

      Originally posted by damiankao View Post
      I just finished mapping my ABI pair end colorspace reads with tophat. The reads were 50bp F3 and 25bp F5.

      When I tried to convert the .bam file into .sam for Cufflinks assembly using Picard Tools, I got this error:

      Exception in thread "main" java.lang.RuntimeException: SAM validation error: ERROR: Record 127338, Read name 507_970_1560_F3, Mate Alignment start (542169) must be <= reference sequence length (531507) on reference Contig1

      It looks like a read is being "mapped" outside of the reference contig?

      Bowtie has --fr, --rf, --ff options when aligning pair-end reads. Does tophat take into account that SOLiD mate pairs are both in forward direction? so the --ff would be used.
      I also received this error
      Mate Alignment start must be <= reference sequence length on reference
      when trying to run picard to convert to BAM
      was this ever resolved?
      thanks,

      Comment


      • #4
        TopHat

        I was wondering why the inner distance is important in TopHat how it is related to alignment? Any one tried using variable inner distance (-r/--mate-inner-dist <int> ) and check what may be the effect on alignments, if any.

        Comment


        • #5
          I have aligned the reads using tophat version 2, but the error message remain. Why there possible exist the possition longer than the real length, in spite of the seperate alignment of tophat.

          Comment

          Latest Articles

          Collapse

          • seqadmin
            Recent Developments in Metagenomics
            by seqadmin





            Metagenomics has improved the way researchers study microorganisms across diverse environments. Historically, studying microorganisms relied on culturing them in the lab, a method that limits the investigation of many species since most are unculturable1. Metagenomics overcomes these issues by allowing the study of microorganisms regardless of their ability to be cultured or the environments they inhabit. Over time, the field has evolved, especially with the advent...
            09-23-2024, 06:35 AM
          • seqadmin
            Understanding Genetic Influence on Infectious Disease
            by seqadmin




            During the COVID-19 pandemic, scientists observed that while some individuals experienced severe illness when infected with SARS-CoV-2, others were barely affected. These disparities left researchers and clinicians wondering what causes the wide variations in response to viral infections and what role genetics plays.

            Jean-Laurent Casanova, M.D., Ph.D., Professor at Rockefeller University, is a leading expert in this crossover between genetics and infectious...
            09-09-2024, 10:59 AM

          ad_right_rmr

          Collapse

          News

          Collapse

          Topics Statistics Last Post
          Started by seqadmin, 10-02-2024, 04:51 AM
          0 responses
          13 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 10-01-2024, 07:10 AM
          0 responses
          21 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 09-30-2024, 08:33 AM
          0 responses
          25 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 09-26-2024, 12:57 PM
          0 responses
          18 views
          0 likes
          Last Post seqadmin  
          Working...
          X