Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts

  • bioinfosm
    replied
    cool, that was fast!

    Leave a comment:


  • mmartin
    replied
    Good idea. Since this was on my to do list as well, I have just implemented this feature and released cutadapt 0.6.

    Leave a comment:


  • sdavis
    replied
    This looks a very useful tool. Could I suggest that you accept gzipped fastq files as an alternative input format as a simple convenience?

    Leave a comment:


  • HiroMishima
    replied
    Originally posted by mmartin View Post
    Hi, actually, you do have to use two -a options since currently reverse complements are not automatically searched for.

    I managed to reproduce the problem you encountered and I have prepared a new release that hopefully fixes it. You can download v0.4 from the homepage and see whether the bug is actually fixed. Thanks for reporting this!
    Everything's perfect! cutadapt 0.5.1 worked well with two -a options.

    I believe that cutadapt is one of the best adopter sequence trimmer especially in term of simpleness and speed.

    Thanks again for prompt update.

    Leave a comment:


  • mmartin
    replied
    Since this isn't too hard, I just added that feature. cutadapt now has the option "--discard", which does exactly that: If an adapter is found in the read, then the read is discarded and not trimmed.

    Leave a comment:


  • gaffa
    replied
    I haven't looked into the details of the program, but I wonder how straightforward it would be to use the program to filter out and discard the entire reads that match an adapter, rather just removing that part and re-using the trimmed read?

    Leave a comment:


  • mmartin
    replied
    Hi, actually, you do have to use two -a options since currently reverse complements are not automatically searched for.

    I managed to reproduce the problem you encountered and I have prepared a new release that hopefully fixes it. You can download v0.4 from the homepage and see whether the bug is actually fixed. Thanks for reporting this!

    Leave a comment:


  • HiroMishima
    replied
    Originally posted by mmartin View Post
    Could you give an example of the problematic read you encounter and the output of cutadapt for that read?
    I found that I used two -a options and used adapter sequences were almost reverse complement each other. Probably I do not have to use two -a options in this case. Hopefully, these examples clarify the situation.

    sample.fastq:
    Code:
    @read1
    GATCCTCCTGGAGCTGGCTGATACCAGTATACCAGTGCTGATTGTTGAATTTCAGGAATTTCTCAAGCTCGGTAGC
    +
    hhhhhhhhhhahhhhhehhffhghhehdgghhheddggfhfhhgffhddhhfffhhffhfgggffddfdfffcdfb
    @read2
    CTCGAGAATTCTGGATCCTCTCTTCTGCTACCTTTGGGATTTGCTTGCTCTTGGTTCTCTAGTTCTTGTAGTGGTG
    +
    hhhhhhhhhhhhhhhhhhhhhhhhhhgghghhhhhhhhgaddeeadaa^dadaa_aaaaababca_aa__^[T^[Z
    And next result is OK:
    Code:
    $python cutadapt -a CTCGAGAATTCTGGATCCTC sample.fastq
    
    @read1
    CTGGAGCTGGCTGATACCAGTATACCAGTGCTGATTGTTGAATTTCAGGAATTTCTCAAGCTCGGTAGC
    +
    hhhahhhhhehhffhghhehdgghhheddggfhfhhgffhddhhfffhhffhfgggffddfdfffcdfb
    @read2
    TCTTCTGCTACCTTTGGGATTTGCTTGCTCTTGGTTCTCTAGTTCTTGTAGTGGTG
    +
    hhhhhhgghghhhhhhhhgaddeeadaa^dadaa_aaaaababca_aa__^[T^[Z
    However, in next results, read1 still contains "GATCCTC" in the 5' end:
    Code:
    $python cutadapt -a CTCGAGAATTCTGGATCCTC -a GAGGATCCAGAATTCTCGAGTT sample.fastq
    
    @read1
    GATCCTCCTGGAGCTGGCTGATACCAGTATACCAGTGCTGATTGTTGAATTTCAGGAATTTCTCAAGCTCGGTAGC
    +
    hhhhhhhhhhahhhhhehhffhghhehdgghhheddggfhfhhgffhddhhfffhhffhfgggffddfdfffcdfb
    @read2
    TCTTCTGCTACCTTTGGGATTTGCTTGCTCTTGGTTCTCTAGTTCTTGTAGTGGTG
    +
    hhhhhhgghghhhhhhhhgaddeeadaa^dadaa_aaaaababca_aa__^[T^[Z

    Leave a comment:


  • mmartin
    replied
    Yes, cutadapt recognizes partial adapters. That is, if your adapter is ADAPTER and your read is MYSEQUENCEADAP, then the resulting sequence is MYSEQUENCE. In fact, these are some examples of input sequences that will result in MYSEQUENCE:
    MYSEQUENCEADAPTER
    MYSEQUENCEADAP
    MYSEQUENCEADPAPTERSOMETHINGELSE

    Could you give an example of the problematic read you encounter and the output of cutadapt for that read?

    Leave a comment:


  • HiroMishima
    replied
    3'-end partial match of adapters

    Hi,

    I have a question about Cutadapt version 0.3.

    Does Cutadapt cut partial sequences of adapters?

    According to "Statistics for adapter" messages, Cutadapt seems to recognize 3'-end partial match of adapters. However, only full-matched adapter sequences are removed in output files.

    Leave a comment:


  • mmartin
    replied
    Yes, Python 2.6 is needed, thanks for the pointer. It wouldn't be hard to support Python 2.5, but some 2.6 features make the transition to the Python 3 syntax easier, so I would like to stick to it. I have updated the homepage to reflect the requirement of Python 2.6.

    Leave a comment:


  • Torst
    replied
    Originally posted by mmartin View Post
    I'm pleased to announce the tool 'cutadapt
    http://cutadapt.googlecode.com/
    It seems your code only runs under Python 2.6 ?

    For Centos 5.x, which is a bit behind, I had to install the "python26" packages and change the #!/usr/bin/python to #!/usr/bin/python26.

    Leave a comment:


  • mmartin
    started a topic cutadapt: A tool that removes adapter sequences

    cutadapt: A tool that removes adapter sequences

    I'm pleased to announce the tool 'cutadapt', which we have been using in our research group for adapter removal in high-throughput sequencing data. Removing adapter sequences from reads is necessary when the read length of the sequencing machine is longer than the molecule that is sequenced, for example when sequencing small RNAs.

    Since special code is included to handle color space data correctly, the tool may be especially useful for people who do not use Applied Biosystem's Corona pipeline.

    cutadapt is under the MIT license.

    Please see the web page for a feature list and a link to a downloadable package:

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
  • SEQadmin2
    Advanced Sequencing Platforms Tackle Neuroscience’s Toughest Genomics Problems
    by SEQadmin2



    Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
    ...
    07-09-2026, 11:10 AM

ad_right_rmr

Collapse

News

Collapse

Topics Statistics Last Post
Started by SEQadmin2, Today, 07:41 AM
0 responses
9 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 08-03-2026, 10:13 AM
0 responses
25 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 07-31-2026, 02:55 AM
0 responses
38 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 07-24-2026, 12:17 PM
0 responses
25 views
0 reactions
Last Post SEQadmin2  
Working...