Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts

  • JQL
    replied
    another nice way to do it.

    I really think something is going on with my server. It still finished after doing one file. I will ask my admin tomorrow. Will let you know.

    By any chance did this happen to any one of you here?

    Originally posted by Richard Finney View Post
    for i in $(ls *.gz); do sn=`echo $i | sed 's/\.gz$//'`; zcat $i > $sn; done;

    Leave a comment:


  • Richard Finney
    replied
    for i in $(ls *.gz); do sn=`echo $i | sed 's/\.gz$//'`; zcat $i > $sn; done;

    Leave a comment:


  • JQL
    replied
    thanks. I thought it might be related to something internal. will find out.

    Originally posted by azneto View Post
    I tested your version of the command and it worked fine. It could be something related to permissions.

    Leave a comment:


  • azneto
    replied
    I tested your version of the command and it worked fine. It could be something related to permissions.

    Leave a comment:


  • JQL
    replied
    I tried
    for i in `ls *.fastq.gz`; do gunzip -c $i > ${i%.gz}; done

    still only unzipped just first file then finished. no error. very strange.


    Originally posted by azneto View Post
    for i in `ls *.fastq.gz`; do gunzip -c $i > $i.fastq; done

    Leave a comment:


  • azneto
    replied
    for i in `ls *.fastq.gz`; do gunzip -c $i > $i.fastq; done

    Leave a comment:


  • JQL
    replied
    gunzip *.fastq.gz will delete original gz files. i want to keep original files.



    Originally posted by azneto View Post
    have you tried 'gunzip *.fastq.gz' ?

    Leave a comment:


  • azneto
    replied
    have you tried 'gunzip *.fastq.gz' ?

    Leave a comment:


  • JQL
    started a topic bash shell question

    bash shell question

    I tried to do a simple task in batch--unzipping many gz files. I have many .gz files, but how come it only unzipped one file then finished? Anything wrong with my script? thanks. John


    ## unzip fastq.gz
    for i in *.fastq.gz
    do
    #echo $i
    zcat "$i" > "${i%.*}"
    done

Latest Articles

Collapse

  • SEQadmin2
    Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
    by SEQadmin2



    CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).

    Despite this, “CRISPR helped turn genome editing from a specialized technique into
    ...
    07-31-2026, 11:01 AM
  • SEQadmin2
    Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
    by SEQadmin2


    Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

    The systematic characterization of the human proteome has
    ...
    07-20-2026, 11:48 AM

ad_right_rmr

Collapse

News

Collapse

Topics Statistics Last Post
Started by SEQadmin2, 08-06-2026, 07:41 AM
0 responses
14 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 08-03-2026, 10:13 AM
0 responses
31 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 07-31-2026, 02:55 AM
0 responses
40 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 07-24-2026, 12:17 PM
0 responses
26 views
0 reactions
Last Post SEQadmin2  
Working...