Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • cmccabe
    Senior Member
    • Jul 2012
    • 355

    #1

    coordinates to hg19 refseq gene name

    Is there a tool or script that can convert chromsome, start, and end to chromosome, start, end, gene?

    Input: (txt file)
    chr1 955542 955763
    chr1 957570 957852
    chr1 976034 976270

    Output:
    chr1 955542 955763 ...
    chr1 957570 957852 ...
    chr1 976034 976270 ...

    ... is the gene name. Thank you.
  • dpryan
    Devon Ryan
    • Jul 2011
    • 3478

    #2
    There are a number of options for this. One option would be to use GenomicRanges and GenomicFeatures in R. You can also use bedtools or bedops (just use one of the commands that yields the closest feature in a second file and then reparse the output to contain only what you need).

    Comment

    • cmccabe
      Senior Member
      • Jul 2012
      • 355

      #3
      coordinates to hg19 refseq gene name

      Here is what I am trying to do:

      In BedTools get a list of gene names from a list of coordinates:
      chr1 955542 955763
      chr1 957570 957852
      chr1 976034 976270

      (is there a command in BedTools you recomend)?


      create example.bed in UCSC

      In BedTools:

      mergeBed - i example.bed > merged_example.bed

      intersectBed -a example1.bed -b example2.bed > intersected_example.bed


      Basically, I am trying to find a subset of probes (example.bed) in a panel of ~4600 genes (example1.bed). Thank you.

      Comment

      • chrchang
        Member
        • Jun 2013
        • 15

        #4
        The PLINK 1.9 resources page describes how to construct this type of gene list file from UCSC Table Browser output:



        (It sounds like you can skip the final "resort by gene name" steps.)

        Comment

        Latest Articles

        Collapse

        • SEQadmin2
          Multiomic Liquid Biopsy: What DNA/RNA Panels Reveal That DNA Alone Can’t
          by SEQadmin2



          Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?

          Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating
          ...
          10-14-2026, 09:55 AM
        • SEQadmin2
          New Genomics Technologies Take Aim at Long-Standing Limits
          by SEQadmin2


          Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.

          We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing
          ...
          09-28-2026, 10:25 AM

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by SEQadmin2, Yesterday, 11:13 AM
        0 responses
        16 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, Yesterday, 10:48 AM
        0 responses
        16 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-15-2026, 10:52 AM
        0 responses
        35 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-14-2026, 05:39 AM
        0 responses
        42 views
        0 reactions
        Last Post SEQadmin2  
        Working...