Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • ElMichael
    Member
    • Jun 2009
    • 31

    Dataset (PLINK format): conversion from b36 to b37

    Hi,

    I have a dataset in the binary PLINK format from the Illumina 1M array. Samples were genotyped on the array, designed to human genome build 36. But now I need to convert it to b37. What is the best way to do it? I read about some Illumina conversion files but didn't find them.

    Thanks!
  • turnersd
    Senior Member
    • May 2011
    • 115

    #2
    liftOver the map file.

    Comment

    • ElMichael
      Member
      • Jun 2009
      • 31

      #3
      But what is about those snps whose position was changed even to another chromosome? And snps whose rs ID was changed?

      Comment

      • turnersd
        Senior Member
        • May 2011
        • 115

        #4
        I think the liftover would fix the chromosome issue (probably, others? comments?) but not sure about the rs ID mapping.

        Comment

        • ElMichael
          Member
          • Jun 2009
          • 31

          #5
          Thank you, turnersd!

          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, Yesterday, 11:08 AM
          0 responses
          6 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 06-30-2026, 05:37 AM
          0 responses
          11 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 06-26-2026, 11:10 AM
          0 responses
          19 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 06-17-2026, 06:09 AM
          0 responses
          53 views
          0 reactions
          Last Post SEQadmin2  
          Working...