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
      Recent Advances in Sequencing Analysis Tools
      by seqadmin


      The sequencing world is rapidly changing due to declining costs, enhanced accuracies, and the advent of newer, cutting-edge instruments. Equally important to these developments are improvements in sequencing analysis, a process that converts vast amounts of raw data into a comprehensible and meaningful form. This complex task requires expertise and the right analysis tools. In this article, we highlight the progress and innovation in sequencing analysis by reviewing several of the...
      05-06-2024, 07:48 AM
    • 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...
      04-22-2024, 07:01 AM

    ad_right_rmr

    Collapse

    News

    Collapse

    Topics Statistics Last Post
    Started by seqadmin, Yesterday, 06:57 AM
    0 responses
    12 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 05-06-2024, 07:17 AM
    0 responses
    16 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 05-02-2024, 08:06 AM
    0 responses
    19 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-30-2024, 12:17 PM
    0 responses
    24 views
    0 likes
    Last Post seqadmin  
    Working...
    X