Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • papori
    Senior Member
    • Dec 2010
    • 181

    Converting format insurance

    Hi all,
    Probably this is a FAQ, but still i didnt find a good answer..

    I am converting from bam to fastq.
    My bam's are paired end, coordinated sorted and very large (100Gb+).
    For my analysis i need only the first pair.

    Right now i am using these 2 commands:

    For converting bam to sam for the first pair.
    Code:
    samtools view -h -f 0x0040 $line > $line.pe1.sam
    and for parsing the fastq from the sam format.
    Code:
    cat $line.pe1.sam | grep -v ^@ | awk '{print "@"$1"\n"$10"\n+\n"$11}' > $line.pe1.sam.fq
    this i took from:


    How can i be sure that i got all the reads? mapped + unmapped of the first pair?

    Thanks,
    Pap
  • maubp
    Peter (Biopython etc)
    • Jul 2009
    • 1544

    #2
    Samtools does (now) have a BAM to FASTQ option, that might be easier.

    Comment

    • papori
      Senior Member
      • Dec 2010
      • 181

      #3
      Originally posted by maubp View Post
      Samtools does (now) have a BAM to FASTQ option, that might be easier.
      Thanks maubp!!

      Comment

      Latest Articles

      Collapse

      • GATTACAT
        Reply to Nine Things a Sample Prep Scientist Thinks About Before Sequencing
        by GATTACAT
        Love this - good data definitely starts from good input, and poor input can only give relatively poor data. I particularly like the mention of Nanodrop/absorbance based methods for quantification. It's such a toss up if you'll get an accurate reading or what amounts to a randomly generated number, and a lot of library/sequencing related issues can be traced back to poor quant.
        07-01-2026, 11:43 AM
      • SEQadmin2
        Nine Things a Sample Prep Scientist Thinks About Before Sequencing
        by SEQadmin2


        I’m not a sequencing expert. I’m a purification scientist who uses NGS to evaluate workflows my group develops. With this perspective, we think about the sample first and the NGS workflow second. The sequencer is an exceptionally honest reporter, but it can only report on what you give it, so whether you get clean, interpretable data from an NGS workflow is largely determined before you begin.

        Here are nine questions we think about, in roughly the order they matter, before...
        06-18-2026, 07:11 AM

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by SEQadmin2, 07-02-2026, 11:08 AM
      0 responses
      25 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 06-30-2026, 05:37 AM
      0 responses
      23 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 06-26-2026, 11:10 AM
      0 responses
      23 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 06-17-2026, 06:09 AM
      0 responses
      55 views
      0 reactions
      Last Post SEQadmin2  
      Working...