Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Genetic Code Alteration - blastx

    Hi All,

    I'm not sure if I'm in the right forum with this query. But any info would be great!

    I am running blastx on a standalone version of blast-2.2.31+. Using the standard genetic code each stop codon (TAA, TAG, TGA) is represented by the asterisk symbol '*'.

    Is it possible to amend the genetic code to give each stop codon an individual symbol? for example TAA '#', TAG '&', TGA '%'

    Is it possible to supply a uniquely generated genetic code to standalone blastx searches?

    I have read through the literature and have not found examples of such amendments.

  • #2
    You can use some of the predefined genetic code tables defined by the NCBI,

    Code:
    $ blastx -help
    ...
     -query_gencode <Integer, values between: 1-6, 9-16, 21-25>
       Genetic code to use to translate query (see user manual for details)
    ...
    See http://www.ncbi.nlm.nih.gov/Taxonomy/Utils/wprintgc.cgi

    Defining your own would probably required editing the BLAST+ source code and making your own modified blastx tool (i.e. theoretically possible but not easy).

    Comment


    • #3
      Just speculating. It may be easier to check the sequence in the blast hits to differentiate the three codons?

      Comment


      • #4
        Thanks for the suggestion. I'm performing multiple sequence alignments with large data sets >50,000 sequences and hoping to identify stop codon reassignments. However all three stop codons are identified by the '*' symbol so I can't tell them apart.

        Comment


        • #5
          In your case I could think about writing some custom scripts to take the BLAST output and original nucleotide sequences, and map the stop codons to three different symbols.

          (If you are not already, you should think about learning a programming language to help with your research - check out Software Carpentry workshops etc.)

          Comment

          Latest Articles

          Collapse

          • 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
          • seqadmin
            Strategies for Sequencing Challenging Samples
            by seqadmin


            Despite advancements in sequencing platforms and related sample preparation technologies, certain sample types continue to present significant challenges that can compromise sequencing results. Pedro Echave, Senior Manager of the Global Business Segment at Revvity, explained that the success of a sequencing experiment ultimately depends on the amount and integrity of the nucleic acid template (RNA or DNA) obtained from a sample. “The better the quality of the nucleic acid isolated...
            03-22-2024, 06:39 AM

          ad_right_rmr

          Collapse

          News

          Collapse

          Topics Statistics Last Post
          Started by seqadmin, 04-11-2024, 12:08 PM
          0 responses
          25 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-10-2024, 10:19 PM
          0 responses
          27 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-10-2024, 09:21 AM
          0 responses
          24 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-04-2024, 09:00 AM
          0 responses
          52 views
          0 likes
          Last Post seqadmin  
          Working...
          X