Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • Old Pioneer
    Junior Member
    • Jan 2016
    • 1

    #1

    Write the subset of reads from BAM file into new SAM/BAM file, using R tools.

    Hello every one.

    I am new in bioinformatic, and now I try solve the next problem. I have sorted BAM file with paired-end RNA-Seq data (several tens of thousands reads). My work tool is R. I need: 1) Filter this file by "isize" field: extract the reads with isize not equal to NA and with absolute value of isize lower than threshold (in this case, 642 bp); 2) Write this subset into SAM file, because this type is required for package which I will use.

    I tried use R package Rsamtools for this, function filterBam(). Remove reads with isize == NA is possible by means scanBamFlag:
    flag <- scanBamFlag(isPaired = TRUE, hasUnmappedMate = FALSE).

    But I have no idea about filtration by threshold (abs(bamFile$isize) <= 642). How I can do it in R? I do not believe that effective way for this does not exist. Unfortunately, my experience in R and programming for now is inadequate for solve this problem quickly. Can someone to help me? Thanks in advance!

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
31 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 10-22-2026, 10:48 AM
0 responses
22 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 10-15-2026, 10:52 AM
0 responses
39 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 10-14-2026, 05:39 AM
0 responses
45 views
0 reactions
Last Post SEQadmin2  
Working...