Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • Martino
    Member
    • Apr 2011
    • 15

    #1

    Calculating average coverage wih Pysam

    Hi,

    I have to program a program, which calculates each average at each position.

    The idea was that that program was good, but it is too slow. That is why the code must be adapted to get is faster.

    Does someone knows code for that?
  • arvid
    Senior Member
    • Jul 2011
    • 156

    #2
    I'm not sure what you mean by average, if you talk about each position; do you mean each precise position or some kind of window?

    Have a look at "bedtools coverage" and "bedtools genomecov"; I like to use
    Code:
    bedtools genomecov -bg -split -ibam file.bam > file_coverage.bedgraph
    which gives me a BedGraph; if you use "-d" instead of "-bg" you get the read count at each and every position.

    You can get BEDTools here: http://code.google.com/p/bedtools/
    There is also a python interface for it (pybedtools), but I'm not sure whether it makes sense to use it in this case, haven't really tried it.
    Last edited by arvid; 05-29-2012, 04:36 AM. Reason: added link

    Comment

    Latest Articles

    Collapse

    • SEQadmin2
      Multiomic Liquid Biopsy: What DNA/RNA Panels Reveal That DNA Alone Can’t
      by SEQadmin2



      Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?

      Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating
      ...
      10-14-2026, 09:55 AM
    • SEQadmin2
      New Genomics Technologies Take Aim at Long-Standing Limits
      by SEQadmin2


      Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.

      We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing
      ...
      09-28-2026, 10:25 AM

    ad_right_rmr

    Collapse

    News

    Collapse

    Topics Statistics Last Post
    Started by SEQadmin2, 10-22-2026, 11:13 AM
    0 responses
    22 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 10-22-2026, 10:48 AM
    0 responses
    18 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 10-15-2026, 10:52 AM
    0 responses
    36 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 10-14-2026, 05:39 AM
    0 responses
    42 views
    0 reactions
    Last Post SEQadmin2  
    Working...