Announcement

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

  • long repeated elements in a bacterial genome

    if there are say 20 (almost) identical transposons of say 800 bases in a 6 Mbase genome, is there any way an assembler can properly position them using only single reads of 36 bases? and what to think when an assembler gives a bunch of contigs that all finish with a few hundred bases of that transposon?

    RudyS

  • #2
    Originally posted by RudyS View Post
    if there are say 20 (almost) identical transposons of say 800 bases in a 6 Mbase genome, is there any way an assembler can properly position them using only single reads of 36 bases?
    I don't think so.

    and what to think when an assembler gives a bunch of contigs that all finish with a few hundred bases of that transposon?
    Then you've got unique sequence flanked by repeats. You'll never know in what order they all fall without paired ends, or far longer reads.

    Comment


    • #3
      Originally posted by swbarnes2 View Post
      I don't think so.
      More directly, unequivocally no.

      This will require mate pairs with a span greater than 800 bases to resolve.

      -mark

      Comment


      • #4
        maybe its not possible? any other de novo assembler on the horizon?

        so basically its hopeless you think ... because even with paired-end reads 800-1000 base repeated elements are a long stretch? it would seem that the assembler might actually connect inappropriate flanks for the repeats ... in my case it didnt ... but maybe it gets lost in the middle ... what assemblers are people using?

        Comment

        Latest Articles

        Collapse

        • seqadmin
          Advanced Tools Transforming the Field of Cytogenomics
          by seqadmin


          At the intersection of cytogenetics and genomics lies the exciting field of cytogenomics. It focuses on studying chromosomes at a molecular scale, involving techniques that analyze either the whole genome or particular DNA sequences to examine variations in structure and behavior at the chromosomal or subchromosomal level. By integrating cytogenetic techniques with genomic analysis, researchers can effectively investigate chromosomal abnormalities related to diseases, particularly...
          09-26-2023, 06:26 AM
        • seqadmin
          How RNA-Seq is Transforming Cancer Studies
          by seqadmin



          Cancer research has been transformed through numerous molecular techniques, with RNA sequencing (RNA-seq) playing a crucial role in understanding the complexity of the disease. Maša Ivin, Ph.D., Scientific Writer at Lexogen, and Yvonne Goepel Ph.D., Product Manager at Lexogen, remarked that “The high-throughput nature of RNA-seq allows for rapid profiling and deep exploration of the transcriptome.” They emphasized its indispensable role in cancer research, aiding in biomarker...
          09-07-2023, 11:15 PM

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by seqadmin, Yesterday, 09:38 AM
        0 responses
        9 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, 09-27-2023, 06:57 AM
        0 responses
        11 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, 09-26-2023, 07:53 AM
        1 response
        23 views
        0 likes
        Last Post seed_phrase_metal_storage  
        Started by seqadmin, 09-25-2023, 07:42 AM
        0 responses
        17 views
        0 likes
        Last Post seqadmin  
        Working...
        X