Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • cmccabe
    Senior Member
    • Jul 2012
    • 355

    #1

    filter secondary reads in bam with pysam

    I am new to python and trying to learn. The below is an attempt to filter out secondary reads in a all bam files in a directory using pysam. I ran mark duplicates and got an error on several bam files due to secondary alignments. I added comments to each line to illustrate my thought process. Thank you .

    The specific mark duplicates error:

    Value was put into PairInfoMap more than once

    Code:
     
        #! /usr/bin/python  ## call python script
        import sys ## import python system functions
        import pysam  ## import module
    
        bam = pysam.AlignmentFile(.bam, "rb")  ## open bam and read
        click.echo("Reading BAM file")  ## output message
        for read in bam.fetch():
            if read.is_secondary=true  ## not the primary alignment
                continue
            if read.has_tag('AS') and read.has_tag('XS') ## look for Primary and Secondary Alignment Score tag
                AS = read.get_tag('AS')  ## read and store AS value
                XS = read.get_tag('XS')  ## read and store XS value
                     if AS >= XS  ## Alignment score greater then or equal to XS (these will be printed)
                bam.write(read)  ## open bam and only print primary alignments
                     continue  ## process next line
        bam.close()  ## end processing
    another option
    Code:
    #! /usr/bin/python  ## call python script
    import sys ## import python system functions
    import pysam  ## import module
    
    bam = pysam.AlignmentFile(bam, "rb")  ## open bam and read
    click.echo("Reading BAM file")  ## output message
    	for read in bam.fetch():  ## start loop and iterate over each bam
    		if read.is_secondary:  ## not the primary alignment
    			continue
    		if read.has_tag('AS') and read.has_tag('XS') ## look for Primary and Secondary Alignment Score tag
    			AS = read.get_tag('AS')  ## read and store AS value
    			XS = read.get_tag('XS')  ## read and store XS value
    				if AS >= XS  ## Alignment score greater then or equal to XS (these will be printed)
    		read.write(read)  ## only print primary alignments
    		continue
    bam.close()  ## end processing
    Last edited by cmccabe; 04-17-2019, 04:44 AM. Reason: added option 2

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
42 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 10-22-2026, 10:48 AM
0 responses
32 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 10-15-2026, 10:52 AM
0 responses
44 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...