Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • dzmtnvmt
    Member
    • Apr 2010
    • 11

    #1

    how to fetch the snp allele frequency?

    hello,everyone~

    I now need a txt file with several columns, which contains the rs ID of snp, frequency of each allele. I was told to download the SNPAlleleFreq.bcp file from ncbi. But i don't know exactly what each column tells about, and who to fetch the snp allel freq. So i need some help.

    thanks very much
  • epigen
    Senior Member
    • May 2010
    • 101

    #2
    Hi,

    if you haven't found another way yet, I'd recommend downloading the snp130 table from the UCSC genome browser. I suppose you'd like to have SNPs for the latest human genome? Then go to http://hgdownload.cse.ucsc.edu/golde...hg19/database/
    and download snp130.txt.gz

    A description of the columns is available in the "Tables"

    when you select from the dropdown menu
    group: Variations and Repeats track: SNPs (130)
    table: "snp130"
    and then hit "describe table schema"

    Hope this helps

    Comment

    • husamia
      Member
      • Apr 2010
      • 66

      #3
      I have the same question, I am interested in frequency information from dbsnp132. I have chromosomal positions and rs#s and want to get frequency information. My goal is to filter out common snps since 1000genomes data is supposed to discover rare variations <1%.

      Comment

      • megnetz
        Junior Member
        • Jul 2010
        • 4

        #4
        Hello! I checked one biallelic SNP in this database (snp131) to determine allele freq. I found an average heterozygosity of 0.5. I guess this is because there is no data on allele frequency? Or is it actually 0.5? In that case allele frequency should also be 0.5 according to hardy-weinberg?

        Thanks for your help!

        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
        17 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, Yesterday, 10:48 AM
        0 responses
        18 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-15-2026, 10:52 AM
        0 responses
        36 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...