Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • hisat2 output more reads than are in the file

    Hi all,
    I am in the middle of testing the hisat2 mapper and encountered a discrepancy between the output hisat2 gives me at the end of the mapping step and the number of reads samtools flagstat counts.

    this is the output I get, when hisat2 is finished:
    Code:
    cat ../hisat2Mapping/WCE7.stat 
    [B]11389273[/B] reads; of these:
      11389273 (100.00%) were paired; of these:
        5961828 (52.35%) aligned concordantly 0 times
        4647893 (40.81%) aligned concordantly exactly 1 time
        779552 (6.84%) aligned concordantly >1 times
        ----
        5961828 pairs aligned concordantly 0 times; of these:
          138165 (2.32%) aligned discordantly 1 time
        ----
        5823663 pairs aligned 0 times concordantly or discordantly; of these:
          11647326 mates make up the pairs; of these:
            10779117 (92.55%) aligned 0 times
            510907 (4.39%) aligned exactly 1 time
            357302 (3.07%) aligned >1 times
    52.68% overall alignment rate
    @Question - how are the 52.68% are calculated? what reads are being considered here as mapped?

    and this is the number of reads I get, when I run samtools flagstat on the sorted/indexed bam file:
    Code:
    samtools flagstat ../hisat2Mapping/WCE7.sorted.bam
    [B]14328481[/B] + 0 in total (QC-passed reads + QC-failed reads)
    2329052 + 0 secondary
    0 + 0 supplementary
    0 + 0 duplicates
    14328481 + 0 mapped (100.00%:-nan%)
    11999429 + 0 paired in sequencing
    6098403 + 0 read1
    5901026 + 0 read2
    10854890 + 0 properly paired (90.46%:-nan%)
    11407498 + 0 with itself and mate mapped
    591931 + 0 singletons (4.93%:-nan%)
    23248 + 0 with mate mapped to a different chr
    18678 + 0 with mate mapped to a different chr (mapQ>=5)
    As you can see, samtools find more reads than there suppose to be originally in the file.

    Is there a simple explanation for that?

    thanks,
    Assa

  • #2
    52.68% = (2*(4647893+779552+138165) + 510907 + 357302)/(2*11389273)

    Samtools is correct, since if sum the numerator you'll get just under 12 million total alignments, which is exactly what's in the BAM file (14328481-2329052).

    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
    18 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-10-2024, 10:19 PM
    0 responses
    22 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-10-2024, 09:21 AM
    0 responses
    16 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-04-2024, 09:00 AM
    0 responses
    47 views
    0 likes
    Last Post seqadmin  
    Working...
    X