Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Assembling a mixed DNA sample

    Hi all,
    I sequenced (Illumina GAII, 75 bp paired end reads, average insert 250) genomic DNA from a sample which contains both a host's and its parasite's DNA, where it is enriched with the parasite's DNA.

    I'm only interested in assembling the parasite's genome, and it is a non reference genome so I'm doing denovo assembly.

    As a filtering step I removed any of the reads that mapped to the host's EST data (there's no reference genome foe the host either), but that probably only removed protein coding DNA.

    So I'm still stuck with non-coding DNA from the host, which I would like to remove. My thought was that since the reads are enriched with the parasite's DNA, contigs originating from the host should have low coverage.

    The problem is that the assembly, produced using SOAPdenovo, uses Kmers to produce contigs and the result is that 80% of the contigs are as 100 bp short and no read maps to them so they have 0 coverage.

    So my question is how do I work around this problem?
    Should I use a larger Kmer size? Should I assume that these short contigs indeed represent the host's non-coding DNA and just filter them?

    Thanks
    Last edited by rubi; 09-15-2011, 07:23 AM.

  • #2
    Hello,

    Have you tried aligning the reads to the human genome to filter the reads that are from the host? Afterwards, you could counterverify the filtered reads by aligning them to related parasite genomes to make sure you do not miss some parasite sequences.

    In addition, you may want to try the Ray assembler, which also uses K-mers and performs very well with paired data. The use of this assembler may even solve part of you problem, since Ray considers the paired-read context to created contigs from the k-mer-based graph.

    FR

    Comment


    • #3
      If the host-parasite relationship is not obligate, you could sequence just the host genome, assembly it, and use it to filter your existing data. Read depth would serve as an independent validation of this strategy.

      Comment


      • #4
        If you're studying something with exteme's of GC content like Plasmodium falciparum (~20%) you might be able to discriminate on GC content.

        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
        39 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