Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • Richard Finney
    Senior Member
    • Feb 2009
    • 701

    unencumbered haplotype estimation

    The problem is this:

    A = homozygous reference
    B = heterzygous
    C = homozygous non-reference

    rows are samples, columns are genomic position
    header row is labels, data is ordered by genomic position
    This data is contrived.

    The data:

    123456789
    ABAAAAABC
    ABCAAAABC
    ABCAAAABC
    BBAAAAABA
    ABCAABABC
    ABCAAAABC
    BBCAAACBC
    ABCAAAABC

    The x and y dimensions can get very large (1000x10000 for example).

    I want to develop an open source, graphical tool to browse this data.
    The core code could be ported anywhere but the first implementation would be for cgi/html/html5 I want a user to be able to mouse over a column and see what's in "linkage disequilibrium" (LD) with that particular genomic position. Speed, usability and reasonable accuracy are critical specs.

    The problem, is, of course "phasing" (or whatever it's called) the B (heterzygous) calls so that LD can be calculated.

    The questions are: what is the best non-patented algorithm for this? "Un-encumbered" by patent is fine, that is if it is patented but unrestricted license is granted. Also, is there an implementation I could check my results with? GPL/LGPL/MIT/DWTFYW whatever is fine. I can port anything to the target language (C for absolute speed).

    This would be a great tool for checking out GWAS results using the newly emerging NGS data sets: "what else is near that sneaky little problem snp?"
  • husamia
    Member
    • Apr 2010
    • 66

    #2
    I think this is great project. Its going to take sometime to think about it.

    The big question is phasing. Do you or not know the phase?
    I seems from your post that you don't know the phase then do you want to infer it bioinformatically using basic assumptions? Refer to phase indifference problem Check out PHASE- Stephen lab for implementation of current methods.

    the most simplistinc problem is you have child, and two parents then assumptions> then infer the phase for homozygous in either one the hets in both parents is not possible.

    This is a big problem and I think best way is to assume you know phase and go from there.

    If you interested in persuing this further need to spend more time and discussion.

    Can you give a visual representation of what the page looks like in your mind as example for clarification?
    Last edited by husamia; 02-05-2012, 03:37 PM.

    Comment

    • Richard Finney
      Senior Member
      • Feb 2009
      • 701

      #3
      Thanks husamia. I checked out Stephens Lab. It does appear to be excellent work; but I want to avoid serious licensing or patent issues; I see this : http://depts.washington.edu/uwc4c/ex...ets/fastphase/
      With words like : The conditions and financial terms of this license apply only to those who download the license, sign it and return it "as is" to the UW Center for Commercialization. Some Express Licenses may be modified for an additional cost. Other licensing arrangements may be available.

      What'd I'd want is something more open, less cumbersome.

      Comment

      • greekkey
        A good person
        • Sep 2012
        • 11

        #4
        Hi, Richard, Are you still going on with your haplotype phasing project?

        Comment

        • Richard Finney
          Senior Member
          • Feb 2009
          • 701

          #5
          No. Its' one of about 6 projects I could get done if I had 2 more hours a day.
          I didn't get very far with it.

          Though if I were doing it now I'd use webassembly.

          Comment

          Latest Articles

          Collapse

          • 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
          • SEQadmin2
            From Collection to Sequencing: Why Sample Preparation and Preservation Define Sequencing Data
            by SEQadmin2


            Data variability is still an issue in sequencing technologies despite the advances in reproducibility and accuracy of these platforms. But the problem does not originate in the sequencing itself, but in the previous steps, before the sample reaches the sequencer.


            The first step is collection, followed by preservation and sample preparation for analysis. Most scientists overlook those steps, but not being careful might just be skewing the experiment’s results.
            ...
            06-02-2026, 10:05 AM

          ad_right_rmr

          Collapse

          News

          Collapse

          Topics Statistics Last Post
          Started by SEQadmin2, 06-17-2026, 06:09 AM
          0 responses
          36 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 06-09-2026, 11:58 AM
          0 responses
          99 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 06-05-2026, 10:09 AM
          0 responses
          120 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 06-04-2026, 08:59 AM
          0 responses
          113 views
          0 reactions
          Last Post SEQadmin2  
          Working...