Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • stampy output

    Hi,

    I get the following information using stampy

    stampy...
    stampy: # Nucleotides (all/1/2): 408825780 204412890 204412890
    stampy: # Variants: 5721043 2786247 2934796
    stampy: # Fraction: 0.0140 0.0136 0.0144
    stampy: # Paired-end insert size: 167.0 +/- 25.7 (1884265 pairs)
    stampy: Done

    Could anyone give me an explanation about the nucleotides, variants and fraction line ?

    Thanks in advance

  • #2
    Nucleotides = Nucleotides aligned
    - All = All reads
    - 1 = Forward reads
    - 2 = Reverse reads
    Variants = Non-reference bases aligned (ie. SNPs and such)
    - All three as before
    Fraction = Fraction of variants discovered in the total number of bases aligned
    Paired-end Insert size = The distance/size of DNA insert between the two adaptors
    [For adaptor]-ForwardRead----->------------<------ReverseRead-[Rev adaptor]

    Comment


    • #3
      Thanks so much

      Comment


      • #4
        I've just finished running Stampy for the first time. I've got the following output:


        stampy: Mapping...
        stampy: # Nucleotides (all/1/2): 9581823944 4790911972 4790911972
        stampy: # Variants: 811646897 406424420 405222477
        stampy: # Fraction: 0.0847 0.0848 0.0846
        stampy: # Paired-end insert size: 141.5 +/- 42.7 (29776104 pairs)
        stampy: Done

        And an output file. What format is the output file in? I didn't specify while running stumpy - I assume it's SAM?

        What's the next step from here, I can't run Samtools flagstat on my output file - this would be really useful as I'm trying to compare the % reads mapped using bowtie and stumpy.

        Any insight would be hugely appreciated!

        N

        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...
          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
        56 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, 04-10-2024, 10:19 PM
        0 responses
        52 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, 04-10-2024, 09:21 AM
        0 responses
        45 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, 04-04-2024, 09:00 AM
        0 responses
        55 views
        0 likes
        Last Post seqadmin  
        Working...
        X