Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • Shorash
    Member
    • Sep 2012
    • 18

    KaKs calculator help (merging fasta files)

    Hi guys,

    I'm trying to merge and align 2 fasta files to get them into quasi-axt format for kaks calculations. The two fasta files are very large ~6 gigabases each. I'm not sure what program allows me to combine and align the two. Any help would be appreciated, here's a link to the example provided by the calculator.

  • Shorash
    Member
    • Sep 2012
    • 18

    #2
    anyone used it before?

    Comment

    • GenoMax
      Senior Member
      • Feb 2008
      • 7142

      #3
      Are these multiple fasta files or just 2 large fasta files with single sequence in each?

      I wonder if you can use the LASTZ aligner to get the AXT format files: http://www.bx.psu.edu/~rsharris/lastz/

      Comment

      • Shorash
        Member
        • Sep 2012
        • 18

        #4
        Originally posted by GenoMax View Post
        Are these multiple fasta files or just 2 large fasta files with single sequence in each?

        I wonder if you can use the LASTZ aligner to get the AXT format files: http://www.bx.psu.edu/~rsharris/lastz/
        I have two separate large fasta files for two species that I wish to use in the kaks calculator. Each file contains assembled pair end reads for the respective species.

        Comment

        • k-gun12
          Member
          • Feb 2010
          • 56

          #5
          You won't be able to just align nucleotide contigs and run the KaKs calculator.. it needs a codon alignment as input.. i.e properly aligned CDS sequence with no UTR and/or indels. A single indel will destroy the alignment. I usually use a combination of estwise and translatorx.

          Comment

          Latest Articles

          Collapse

          • GATTACAT
            Reply to Nine Things a Sample Prep Scientist Thinks About Before Sequencing
            by GATTACAT
            Love this - good data definitely starts from good input, and poor input can only give relatively poor data. I particularly like the mention of Nanodrop/absorbance based methods for quantification. It's such a toss up if you'll get an accurate reading or what amounts to a randomly generated number, and a lot of library/sequencing related issues can be traced back to poor quant.
            07-01-2026, 11:43 AM
          • SEQadmin2
            Nine Things a Sample Prep Scientist Thinks About Before Sequencing
            by SEQadmin2


            I’m not a sequencing expert. I’m a purification scientist who uses NGS to evaluate workflows my group develops. With this perspective, we think about the sample first and the NGS workflow second. The sequencer is an exceptionally honest reporter, but it can only report on what you give it, so whether you get clean, interpretable data from an NGS workflow is largely determined before you begin.

            Here are nine questions we think about, in roughly the order they matter, before...
            06-18-2026, 07:11 AM

          ad_right_rmr

          Collapse

          News

          Collapse

          Topics Statistics Last Post
          Started by SEQadmin2, 07-02-2026, 11:08 AM
          0 responses
          14 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 06-30-2026, 05:37 AM
          0 responses
          15 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 06-26-2026, 11:10 AM
          0 responses
          20 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 06-17-2026, 06:09 AM
          0 responses
          54 views
          0 reactions
          Last Post SEQadmin2  
          Working...