Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • how to get the genome coverage of assembly result

    I want to get the genome coverage of assembly contigs.
    This is a simulated dataset , so I have reference genome.
    I got assembly contigs using Velvet, but I don't know how the contig is correct or wrong. If I using blast aligned the contigs to reference genomes, how do i decide the correct contig or wrong contig? if one contig part aligned to reference genome, how should I do?

    thanks

  • #2
    You can always aling your reads against your contigs and determine any inconsistencies. The group at the Broad Institute proposed in their ALLPATHS papers other ways to evaluate assemblies.

    Leo
    L. Collado Torres, Ph.D. student in Biostatistics.

    Comment


    • #3
      take a look at vmatch
      The Vmatch large scale sequence analysis software is a versatile software tool for efficiently solving large scale sequence matching tasks.

      Comment


      • #4
        You can take a look at QUAST as well. It computes all the metrics.

        Download QUAST for free. Quality Assessment Tool for Genome Assemblies. QUAST performs fast and convenient quality evaluation and comparison of genome assemblies. QUAST computes a number of well-known metrics, including contig accuracy, number of genes discovered, N50, and others, as well as introducing new ones, like NA50 (see details in the paper and in the manual).

        Comment


        • #5
          You want coverage for contigs? Use MIRA. It spits out a file called contig stats, where you got average coverage, max coverage, gc content and other info for every contig produced.

          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