Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts

  • HESmith
    replied
    AAATTT: reverse complement is the same.
    AAAATTT: reverse complement is AAATTTT.

    Leave a comment:


  • biotech
    replied
    Originally posted by krobison View Post
    Note that most assemblers prefer/demand odd length kmers, so that no kmer is its own reverse complement. Programs using kmers for other purposes may not impose that restriction.
    Could you explain this?
    I do not see why it has to be an odd number.
    Perhaps with a simple example.

    Leave a comment:


  • joskee
    replied
    Originally posted by krobison View Post
    17 is an arbitrary size. Depending on the assembler, the length of the reads, and their quality, quite frequently much higher values will give you better assembles.

    Note that most assemblers prefer/demand odd length kmers, so that no kmer is its own reverse complement. Programs using kmers for other purposes may not impose that restriction.
    Ok, I see what you mean.
    I allready had that idea.
    The odd numbered lenght kmers sounds logical! Good you told me, I would not have figured that out myself I think.

    Leave a comment:


  • krobison
    replied
    17 is an arbitrary size. Depending on the assembler, the length of the reads, and their quality, quite frequently much higher values will give you better assembles.

    Note that most assemblers prefer/demand odd length kmers, so that no kmer is its own reverse complement. Programs using kmers for other purposes may not impose that restriction.

    Leave a comment:


  • joskee
    replied
    Originally posted by mastal View Post
    L is the length of the read in base pairs, and yes, the k-mer is a piece of the read.

    For example, if you had a read that was 50 bp long, and wanted to use k-mers of length 47, then you would get 50-47+1=4 kmers from your read.

    The first kmer would be bases 1-47 of the read, the second kmer would be bases 2-48 of the read, the third kmer bases 3-49 and the fourth one bases 4-50, assuming you were also using a step size of 1.

    Are you doing de novo assembly?
    Ah ok.
    It also said: Typically, K = 17.
    So I guess they use 17 as a stanard length.

    I am not doing it myself, we are doing it with the help of a company that does it for us.

    But indeed, the goal is a de novo assembly.

    Leave a comment:


  • mastal
    replied
    Question in terminology

    L is the length of the read in base pairs, and yes, the k-mer is a piece of the read.

    For example, if you had a read that was 50 bp long, and wanted to use k-mers of length 47, then you would get 50-47+1=4 kmers from your read.

    The first kmer would be bases 1-47 of the read, the second kmer would be bases 2-48 of the read, the third kmer bases 3-49 and the fourth one bases 4-50, assuming you were also using a step size of 1.

    Are you doing de novo assembly?

    Leave a comment:


  • joskee
    replied
    Originally posted by JackieBadger View Post
    Length in bases Id guess.. Makes sense
    Yes I know its a length of bases, but what does it represent?

    What is the L bp in relationship to the K-mer?

    Is the K-mer a piece of the L bp ?

    Leave a comment:


  • JackieBadger
    replied
    Length in bases Id guess.. Makes sense

    Leave a comment:


  • joskee
    started a topic Question in terminology

    Question in terminology

    Dear all,

    I received a file with some explenation about a sequence, however there is something I dont understand.


    "A K-mer refers to an artificial sequence division of K nucleotides. A raw sequencing read with L bp contains (L-K+1) K-mers if the length of each K-mer is K bp. The frequency of each K-mer can be calculated from the raw genome sequencing reads"

    I know what a K-mer is, but where do they get the L bp from?
    What is this L bp?

Latest Articles

Collapse

  • 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, detection...
    Yesterday, 06:46 AM
  • 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

ad_right_rmr

Collapse

News

Collapse

Topics Statistics Last Post
Started by SEQadmin2, 10-28-2026, 09:57 AM
0 responses
25 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 10-28-2026, 09:51 AM
0 responses
15 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 10-22-2026, 11:13 AM
0 responses
71 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 10-22-2026, 10:48 AM
0 responses
48 views
0 reactions
Last Post SEQadmin2  
Working...