Seqanswers Leaderboard Ad

Collapse

Announcement

Collapse
No announcement yet.
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • Query on K-mer using in velvet

    Hi, I am newbie to NGS. TO assemble a genome i started using velvet. During which I came across a term called 'K-mer' which means the overlapping segment in the reads. I would like to know that if the K-mer length assigned is suppose 21, is it that the overlapping is done exactly for 21 nucleotides at the ends or is it a minimum requirement for the reads to match? Could i kindly know the difference..Thanks in advance..

  • #2
    Hi!

    A read is hashed into your defined k-mers. And only ends are considered of the k-mers, simply because you are stripping the read.

    Say you have a 10bp read, and a k-mer of 5bp, the hashing of the read into kmers will be;

    read: ACGATGATAGTA
    kmer: ACGAT
    kmer: .CGATG
    kmer: ..GATGA
    kmer: ...ATGAT
    kmer: ....GATAG
    kmer: .....ATAGT
    kmer: ......TAGTA

    The program than finds k-1 overlap (thus here: 5-1=4 bp overlap) at the ends of the k-mers.

    E.g:
    ACGAT
    .CGATG


    So you find overlap at the ends of the k-mers, but within the reads.

    Have a look at this poster from Velvet for maybe detailed information;



    Regards,
    Boetsie

    Comment


    • #3
      thank you..My doubt is cleared..

      Comment

      Latest Articles

      Collapse

      • seqadmin
        Essential Discoveries and Tools in Epitranscriptomics
        by seqadmin


        The field of epigenetics has traditionally concentrated more on DNA and how changes like methylation and phosphorylation of histones impact gene expression and regulation. However, our increased understanding of RNA modifications and their importance in cellular processes has led to a rise in epitranscriptomics research. “Epitranscriptomics brings together the concepts of epigenetics and gene expression,” explained Adrien Leger, PhD, Principal Research Scientist on Modified Bases...
        Yesterday, 07:01 AM
      • seqadmin
        Current Approaches to Protein Sequencing
        by seqadmin


        Proteins are often described as the workhorses of the cell, and identifying their sequences is key to understanding their role in biological processes and disease. Currently, the most common technique used to determine protein sequences is mass spectrometry. While still a valuable tool, mass spectrometry faces several limitations and requires a highly experienced scientist familiar with the equipment to operate it. Additionally, other proteomic methods, like affinity assays, are constrained...
        04-04-2024, 04:25 PM

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by seqadmin, 04-11-2024, 12:08 PM
      0 responses
      37 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 04-10-2024, 10:19 PM
      0 responses
      41 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 04-10-2024, 09:21 AM
      0 responses
      35 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 04-04-2024, 09:00 AM
      0 responses
      55 views
      0 likes
      Last Post seqadmin  
      Working...
      X