Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • qinhao13
    Junior Member
    • Jan 2015
    • 1

    #1

    A strange size difference of fastq file

    Hi, currently I'm working on a Illumina sequencing data in fastq format. I downloaded it from public available database (TCGA) and it was zipped. After unzip and trimming the size of the file is about 16G. Interesting thing comes. After I copied this file to another partition, the size of the new copy became 7.6G. The number of lines in the files, the number of reads and their length distribution are the same in the two files. So I guess the two files have the same content, the new copy is not truncated.

    Moreover, when I run Tophat2/Cufflinks with 16G copy, it takes much longer time to finish and the the result looks strange. But it is quite normal with the 7.6G copy. This might not be a bioinformatics question but it's quite interesting. What happened to the file? What might be those additional size in the file?

    Thanks a lot.
  • dariober
    Senior Member
    • May 2010
    • 311

    #2
    I can't tell... But one thing you can try to get some hints is:

    Code:
    cat -vet my_strange_reads.fq | less
    This is will show you non-printable characters in the file. In a typical fastq file you shouldn't see anything new in addition to the usual alphanumeric characters and some metacharacters in the read names.

    In practice, I would download again the file just to make sure something got corrupted in the process.

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