Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • ClemBuntu
    Member
    • Dec 2014
    • 37

    #1

    How filter bcl2fastq reads ?

    Hello everyone,

    I got a nextseq run that I demultiplexed using bcl2fastq.
    Then I used fastq illumina filter and I got this strange result :

    fastq_illumina_filter (--keep N) statistics:
    Input: 141,900,316 reads
    Output: 141,900,316 reads (9%)
    According to the website where I've downloaded this software :
    This program can filter FASTQ files produced by CASAVA 1.8
    Indeed, all my reads (the 4 lanes) have the "N" tag I checked with the following command
    grep -A 3 '^@.* [^:]*:Y:[^:]*:'
    Why all my reads have the "N" tag ? According to the bcl2fastq user guide this tag DOES exist with bcl2fastq ! (page 22) So, is there a way to filter reads which are produced with bcl2fastq ? Do I have to update the RTA version ? And finally why fastq_illumina_filter gave me 9% of read passing filter ?
  • GenoMax
    Senior Member
    • Feb 2008
    • 7142

    #2
    Forgive me if I am not understanding your question.

    Only way to get "failed" reads in output file is to run bcl2fastq with the option "--with-failed-reads".

    By default N stands for NOT filtered i.e. of good quality.

    Comment

    • ClemBuntu
      Member
      • Dec 2014
      • 37

      #3
      Originally posted by GenoMax View Post
      Only way to get "failed" reads in output file is to run bcl2fastq with the option "--with-failed-reads".
      That's why I wasn't able to see them, thanks

      Comment

      Latest Articles

      Collapse

      • kinpict.com
        Reply to 16S/ITS Profiling vs. Shotgun Metagenomics: What Changes in Your Workflow?
        by kinpict.com
        The part about this topic feels surprisingly grounded, and the details on the page is the bit that made me slow down. I’d keep <a href="https://kinpict.com/">ai family photo generator</a> bookmarked for later.
        Today, 06:37 PM
      • SEQadmin2
        16S/ITS Profiling vs. Shotgun Metagenomics: What Changes in Your Workflow?
        by SEQadmin2





        NGS has revolutionized clinical microbiology by offering new ways to identify and surveil pathogens without prior knowledge of the target. One popular approach is 16S rRNA and ITS amplicon sequencing, which targets specific microbial markers. But studies are increasingly incorporating shotgun metagenomics, a technique that sequences all DNA from a sample without targeting specific microbial markers. This approach allows more detailed taxonomic classification,...
        10-30-2026, 06:46 AM

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by SEQadmin2, 11-12-2026, 07:59 AM
      0 responses
      27 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 11-05-2026, 09:25 AM
      0 responses
      35 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 11-03-2026, 11:54 AM
      2 responses
      56 views
      0 reactions
      Last Post kinpict.com  
      Started by SEQadmin2, 10-28-2026, 09:57 AM
      0 responses
      175 views
      0 reactions
      Last Post SEQadmin2  
      Working...