Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • Ash
    Member
    • Jun 2010
    • 15

    #1

    Help with Standalone Blast

    Hi all,

    I have managed to install standalone blast on my computer and it appears to be working correctly. The output file I get (and I have tried a number of different options) never tells me the number of hits my query has against the database I have created, unlike the online ncbi version of blast - is there any way to make standalone blast tell you this?

    Also, it seems to make no difference changing the "-v" and "-b" parameters. I know from the online version that I should be getting approximately 4500 hits, but I don't seem to be able to get standalone blast to display them all - any thoughts as to how I can make it do this?

    All help gratefully received!

    PS this is using blastall -p blastn
  • maubp
    Peter (Biopython etc)
    • Jul 2009
    • 1544

    #2
    Originally posted by Ash View Post
    PS this is using blastall -p blastn
    That means you are using the old "legacy" BLAST written in C, not the new BLAST+ tools written in C++, which is what the NCBI website is running now.

    Also whenever you get different results to the website, check the parameters carefully. Quite often the website uses different defaults for things like gap settings.

    Comment

    • Ash
      Member
      • Jun 2010
      • 15

      #3
      Many thanks for your response.

      The parameters are identical in the 2 searches (online and standalone) - I think perhaps the difference is that I'm using legacy blast and not the BLAST+ that the NCBI website is running.

      Can anyone running the new BLAST+ (standalone) tell me if it will
      i) Give you the number of hits against your database (like the online BLAST does)?
      ii) Allow you to relatively easily create your own databases to search (I note from the literature that the formatdb command has been replaced with the makeblastdb command?
      iii) Will databases created with the older legacy BLAST be usable with the new BLAST+?

      All help gratefully received!

      A

      Comment

      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, Yesterday, 12:22 PM
      0 responses
      12 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 08-11-2026, 10:35 AM
      0 responses
      13 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 08-06-2026, 07:41 AM
      0 responses
      31 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 08-03-2026, 10:13 AM
      0 responses
      48 views
      0 reactions
      Last Post SEQadmin2  
      Working...