Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts

  • mike.t
    replied
    This is a great opportunity for you to learn to program in Python or Perl!

    Leave a comment:


  • atcghelix
    replied
    I'm not sure what the particulars of your experiment are. I'm often dealing with targeted sequencing, where we are trying to sequence a subset of a few thousand regions of a genome. For something like this, evaluating the best assembly is a little tricky. For each assembly kmer value, I blast my target regions against the assembly. I want to find the assembly that:

    1) matches as many target regions as possible (i.e. lowest number of "No hits found" in the blast report)
    2) maximizes the number of target regions that have contigs that match along their entire length (if a target region is 300 basepairs long, I want assemblies that make contigs where the alignment between the target and the contig is 300 base pairs long, or as close as possible).

    This is more involved than counting with grep. It involves going through each blast query, denoting how long the query sequence is, getting the length of the alignment for the longest hit, and comparing the two. I use Bio::SearchIO from the bioPerl package for this sort of thing.

    I'm not sure what the standard is, or if there is an agreed upon protocol for evaluating assemblies where the goals are more complex than maximizing N50. It's an active area of research for sure (i.e. http://www.biomedcentral.com/1471-2164/14/465). It may be appropriate to merge assemblies from different kmer values as well then reevaluate--something else to look into.

    Leave a comment:


  • milo0615
    replied
    Originally posted by atcghelix View Post
    I'm not sure--it sort of depends on what you want to know. Short kmer values will probably have more hits overall, but the hits will be shorter. I often am trying to find the assembly kmer value that has the highest number of hits that fully span the length of the query sequence.

    If you just want to see how many 'No hits found' there are, you can use:
    grep -c 'No hits found' <filename>
    So you find the best kmer assembly based on the "highest number of hits?" I just want to know which is the best optimal kmer assembly by blasting it against COGS, or should I pick the best hits based on the e-value? How do you pick your best kmer?

    Leave a comment:


  • atcghelix
    replied
    I'm not sure--it sort of depends on what you want to know. Short kmer values will probably have more hits overall, but the hits will be shorter. I often am trying to find the assembly kmer value that has the highest number of hits that fully span the length of the query sequence.

    If you just want to see how many 'No hits found' there are, you can use:
    grep -c 'No hits found' <filename>

    Leave a comment:


  • milo0615
    replied
    Originally posted by atcghelix View Post
    When you say you want the assembly with the most hits, do you mean the assembly that had the fewest number of "no hits found" (i.e. perfect score is 2500--each had at least one hit), or the assembly with the most hits (each of the 2500 COGS have multiple hits---perfect score would be way more than 2500 total hits).
    I would say the assembly that had the fewest number of "no hits found." Do you think that would be a better selection?

    Leave a comment:


  • atcghelix
    replied
    When you say you want the assembly with the most hits, do you mean the assembly that had the fewest number of "no hits found" (i.e. perfect score is 2500--each had at least one hit), or the assembly with the most hits (each of the 2500 COGS have multiple hits---perfect score would be way more than 2500 total hits).

    Leave a comment:


  • milo0615
    started a topic Blast Output Results Analysis

    Blast Output Results Analysis

    Hello,

    I have successfully blasted 2500 merged COGS against 40 different assembly databases. However, I now have 40 large blast results which I need to analyze and select the assembly with the most hits. My questions are the following:

    - What would be the best way or the best practice to analyze all of the blast results to check for the assembly with the most hits?

    - Is there a free application that would help with the analysis?

    Thank you in advance.

Latest Articles

Collapse

  • SEQadmin2
    Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
    by SEQadmin2



    CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).

    Despite this, “CRISPR helped turn genome editing from a specialized technique into
    ...
    07-31-2026, 11:01 AM
  • SEQadmin2
    Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
    by SEQadmin2


    Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

    The systematic characterization of the human proteome has
    ...
    07-20-2026, 11:48 AM

ad_right_rmr

Collapse

News

Collapse

Topics Statistics Last Post
Started by SEQadmin2, 08-13-2026, 12:22 PM
0 responses
28 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 08-11-2026, 10:35 AM
0 responses
22 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 08-06-2026, 07:41 AM
0 responses
37 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 08-03-2026, 10:13 AM
0 responses
51 views
0 reactions
Last Post SEQadmin2  
Working...