Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • Hyunmin
    Member
    • Feb 2012
    • 13

    Using lastz (FAILURE: in load_fasta_sequence)

    This is my lastz command
    $ lastz hg19/chrAll.fa[multiple] merged.fsa

    Error
    FAILURE: in load_fasta_sequence for hg19/chrAll.fa, sequence length 2,084,766,314+115,169,878 exceeds maximum (2,147,483,637)

    I got the error in above.

    What's wrong thing?

    Thanks,
  • GenoMax
    Senior Member
    • Feb 2008
    • 7142

    #2
    Have you tried to do the comparison choosing a smaller set of chromosomes from hg19 at a time and checking if that works?

    Comment

    • Bob-Harris
      Member
      • Mar 2014
      • 13

      #3
      Originally posted by Hyunmin View Post
      This is my lastz command
      $ lastz hg19/chrAll.fa[multiple] merged.fsa
      FAILURE: in load_fasta_sequence for hg19/chrAll.fa, sequence length 2,084,766,314+115,169,878 exceeds maximum (2,147,483,637)
      The short answer is you need to use lastz_32 instead of lastz.

      The long answer… the default lastz build can only handle a target up to 2Gbp combined length. This was a conscious design choice (circa 2004), as there is some efficiency gain from limiting the variables that track sequence positions to 31 bits. The lastz_32 build relaxes that constraint so that it can handle a target up to 4Gbp combined length.

      The efficiency gain was more important on machines 10 years ago than it is now, but for backward compatibility I am keeping that as the default behavior. I'll (probably) change this error report on future releases so that it tells the user to consider using lastz_32.

      The issue is discussed in the readme file here:


      Bob H
      (lastz author)

      Comment

      • Hyunmin
        Member
        • Feb 2012
        • 13

        #4
        Originally posted by Bob-Harris View Post
        The short answer is you need to use lastz_32 instead of lastz.

        The long answer… the default lastz build can only handle a target up to 2Gbp combined length. This was a conscious design choice (circa 2004), as there is some efficiency gain from limiting the variables that track sequence positions to 31 bits. The lastz_32 build relaxes that constraint so that it can handle a target up to 4Gbp combined length.

        The efficiency gain was more important on machines 10 years ago than it is now, but for backward compatibility I am keeping that as the default behavior. I'll (probably) change this error report on future releases so that it tells the user to consider using lastz_32.

        The issue is discussed in the readme file here:


        Bob H
        (lastz author)
        sorry, my late thread..

        I solve the problem with upper.
        Thanks!

        Comment

        • dan
          wiki wiki
          • Jul 2008
          • 194

          #5
          I'm trying lastz-1.03.73 from here: http://www.bx.psu.edu/~rsharris/lastz/newer/

          But I don't see lastz_32... Is this now the default behaviour?

          I just tried 'make lastz_32' and it appeared :-D


          Thanks,
          Last edited by dan; 07-21-2016, 06:20 AM.
          Homepage: Dan Bolser
          MetaBase the database of biological databases.

          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
          12 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 06-30-2026, 05:37 AM
          0 responses
          14 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...