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  • Haplotype Softwares

    Hi,

    I need to know about the haplotype construction softwares from genotype. which is the most accurate to be use? I encountered many like Haploview, Phase, SNPHAP but which one is the most accurate to be use?

    Thanks in advance.

  • #2
    A few more questions need to be answered before you can get a useful answer. Here are some I can think of: Do you have data for a full genome, or only a single gene region? Do you have relationship information available (e.g. trios, or a full genealogy)? Is the data restricted to dimorphic variants (e.g. SNPs)? Are you able to split the data into males and females (they have different recombination rates)?

    I've used haploview for graphical demonstrations because it reports both r^2 and D', but I was working on single genes, and did the block structure analysis manually. I don't think Haploview was able to manage whole chromosomes at once a few years ago.

    Just as a heads-up, there are problems (e.g. overlapping blocks, recombination holes, and sub-blocks) which mean you can't always define particular regions as distinct blocks.

    Comment


    • #3
      Hi,

      Thnx for your reply!

      Data is of a single gene region. We will be predicting haplotype from the genotypic data. Data is of SNP's only. Data is regardless of gender.

      I tried to install Haploview but its giving an error message that it is too big to fit in memory. Our main purpose is TO CONSTRUCT HAPLOTYPES.

      Thank You,

      Comment


      • #4
        Looking for articles on Google scholar / pubmed, it doesn't look like there's been much more interest in Haplotype blocks since ~2005 (i.e. after SNPchips came out), so I'd just go with Haploview. But given that that doesn't work....

        Your error suggests either running Haploview in an unexpected way, or a machine mismatch (e.g. Haploview expects a more modern OS). What are the specifications of the computer you are using? What version of Haploview are you using? If running Linux, the output of the following commands would be useful:
        Code:
        uname -a
        java -version
        java -jar <Haploview location>/haploview.jar

        Comment


        • #5
          Yes, thank you so much.

          It starts working now. How can we create the the input files for them? I tried using the SNP's add-in for Excel 2007 but it is now giving some problems. I will input the files in phased haplotypes format. How will I prepare the input files?

          Thanks!

          Comment


          • #6
            File formats accepted for Haploview can be found here:

            Input File Formats Haploview currently accepts input data in five formats, standard linkage format, completely or partially phased haplotypes, HapMap Project data dumps, PHASE format, and PLINK outputs. The program can also automatically fetch phased HapMap data off the HapMap website. It also takes in a separate file with marker position information, as well as several auxiliary input files, described below. The four formats are explained in depth below.


            I found the Linkage format to be the easiest to create from arbitrary SNP data formats. There's a bit more about the format here (PED is the same as Linkage):



            If using Linkage/Ped files, you'll also need an associated MAP file for the markers:



            Plink is able to convert between PED files (one line per individual), transposed PED files (one line per marker), and long-format files (one line per individual/genotype pair), which should cover most of the types of text-based input data you get:




            Some pre-processing may be necessary to get your data into these formats, but it's not too difficult. However, if you're using Excel to create these files, you're probably going to end up getting tied in knots sometime down the track (your "giving some problems" comment is a pointer to this). I'd recommend you convert your .xls files to .csv, and spend a bit of time with R, Perl, or Python to do this.

            Comment


            • #7
              Informative!

              Just one question, PED files can be easily edited in word pad. PED files with the Linkage format can only be created through Python or PERL or is there any alternative way?

              Thx

              Comment


              • #8
                You can create them in wordpad if you're a particularly masochistic person. If you post a few lines of your input data, I can probably whip up a Perl script to do the right thing (or some R code, if you would prefer that).

                Comment


                • #9
                  Actually I am in learning process of Perl and R. If I will write the scipts in WordPad and just store the file with the extension of .ped and .info, will it work?

                  I will also send you some lines of data so that you can send me the perl coding so that I will be able to construct haplotypes.

                  Comment


                  • #10
                    If I will write the scipts in WordPad and just store the file with the extension of .ped and .info
                    This will work, as long as you keep with the conventions (i.e. space or tab-separated columns). The important thing to make sure about is that the first column is unique for each individual (assuming they're unrelated), and the next five columns are all numeric. If you don't have any other information about individuals, you can set the Individual ID to 1, and the remainder to 0. I prefer setting the phenotype column to 1, because it makes it easier to distinguish where the genotypes start if there are any unknowns:
                    Code:
                    IND001 1 0 0 0 1  A A  G G  A C
                    IND002 1 0 0 0 1  0 0  A G  A A
                    Haploview doesn't care about the file extensions, but using .ped and .map for your PED file and MAP file respectively is a good idea.

                    Comment


                    • #11
                      Perfect!

                      I will just start my work now and if I encounter any problem then I will be looking forward for your help once again

                      Thank you so much.....

                      Comment


                      • #12
                        Hi again!

                        I have done with large data set but now I have set of data which is very small from which Haploview is unable to draw the Haplotypes and LD plots as the data set is small. I have tried Haplotype Inference technique also but failed.

                        I have also done through one algortihm as mentioned in the following link:


                        I just want to be sure as if they are 60 samples or more but if only two values are present like 0 and 1, the possible haplotypes can only be (0,0),(0,1),(1,0),(1,1), in simple terms. Am I going in the right way? *-)

                        Comment


                        • #13
                          I just want to be sure as if they are 60 samples or more but if only two values are present like 0 and 1, the possible haplotypes can only be (0,0),(0,1),(1,0),(1,1), in simple terms. Am I going in the right way? *-)
                          If there's a single variant in a diploid chromosome, there are only two possible haplotypes. Any haplotyping program will only consider a locus interesting if there are observed (or inferred) [substantially] fewer than the expected number of haplotypes.

                          You can force Haploview to display all common haplotypes within a region using a custom block by dragging (in the LD view) across the markers of interest. The definition of common can be adjusted in the haplotype parameters (something like minimum haplotype frequency).
                          Last edited by gringer; 12-21-2011, 03:40 AM. Reason: Whoops, only 2 possible haplotypes at a single dimorphic locus (not 4)

                          Comment


                          • #14
                            Sounds fine. Because my data is somewhat look like this: (only one pair)

                            Sample1 11
                            Sample2 00
                            Sample3 01

                            The custom dragging in the LD Plot is not possible as the LD plot is not created (data set is too small). I have done this custom dragging with other samples available.

                            Comment


                            • #15
                              The custom dragging in the LD Plot is not possible as the LD plot is not created (data set is too small). I have done this custom dragging with other samples available.
                              Then you probably have markers that have been flagged to be ignored for some reason. Go to the marker tab and see if there are any red fields for those markers (this will explain why the marker was excluded. Check the 'rating' box for your markers, and they should be included and appear in the LD plot.

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