Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • htseq-count error with tophat input

    Hi all
    When using htseq-count with sam-files from tophat and gff files from cufflinks, i got following error:

    Error occured in line 1 of file /home/ubelix/sm/mm08c348/counts/ilc31se.sorted.sam.
    Error: Strand must be'+', '-', or '.'.
    [Exception type: ValueError, raised in _HTSeq.pyx:72]

    cmd: htseq-count -t transcript -i ID -s no file.sam cufflinks.gff' > htseq-count

    I checked for the strands in gff file, they look ok (either . - or +). sam file was sorted using sort -n on the bam precursor, so should be ok.
    Any help on this issue would be appreciated!!
    Thank you!
    Michel

  • #2
    I'm currently having exactly same error for name-sorted SAM version of tophat generated BAM file.

    How did you solve this problem then?

    Comment


    • #3
      Hello,

      I am having the same problem. Here is the error and the first line of the file in question (paths redacted):

      Error occured in line 1 of file HC25_4-1_ZT02_1_combined_2.sam.
      Error: Strand must be'+', '-', or '.'.
      [Exception type: ValueError, raised in _HTSeq.pyx:71]

      head -1 HC25_4-1_ZT02_1_combined_2.sam

      HWI-ST1083:106:C1G1MACXX:2:1113:20418:56674:1:N:0:GTGAAA 272 chr2L 49M * 0 0 GACAATGCACGACAGAGGAAGCAGAACAGATATTTAGATTGCCTCTCAT hhiihhfgcggfiiihiifhhiiiihihhiiiiiiigggggeeeeebb_ AS:i:0 XN:i:0 XM:i:0 XO:i:0 XG:i:0 NM:i:0 MD:Z:49 YT:Z:UU NH:i:20 CC:Z:= CP:i:4124 HI:i:0


      Any advice on the matter would be appreciated.

      Comment


      • #4
        GFF files contain strand information as '+' and '-', SAM files don't. Maybe you have passed the two file names in the wrong order.

        Comment


        • #5
          Originally posted by alanlhutchison View Post
          Hello,

          I am having the same problem. Here is the error and the first line of the file in question (paths redacted):

          Error occured in line 1 of file HC25_4-1_ZT02_1_combined_2.sam.
          Error: Strand must be'+', '-', or '.'.
          [Exception type: ValueError, raised in _HTSeq.pyx:71]

          head -1 HC25_4-1_ZT02_1_combined_2.sam

          HWI-ST1083:106:C1G1MACXX:2:1113:20418:56674:1:N:0:GTGAAA 272 chr2L 49M * 0 0 GACAATGCACGACAGAGGAAGCAGAACAGATATTTAGATTGCCTCTCAT hhiihhfgcggfiiihiifhhiiiihihhiiiiiiigggggeeeeebb_ AS:i:0 XN:i:0 XM:i:0 XO:i:0 XG:i:0 NM:i:0 MD:Z:49 YT:Z:UU NH:i:20 CC:Z:= CP:i:4124 HI:i:0


          Any advice on the matter would be appreciated.
          I suspect that you're putting the SAM file were the annotation file should go. The SAM file goes before the annotation file in the command.

          Comment

          Latest Articles

          Collapse

          • 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 on Modified Bases...
            Yesterday, 07:01 AM
          • 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

          ad_right_rmr

          Collapse

          News

          Collapse

          Topics Statistics Last Post
          Started by seqadmin, 04-11-2024, 12:08 PM
          0 responses
          37 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-10-2024, 10:19 PM
          0 responses
          41 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-10-2024, 09:21 AM
          0 responses
          35 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-04-2024, 09:00 AM
          0 responses
          54 views
          0 likes
          Last Post seqadmin  
          Working...
          X