Seqanswers Leaderboard Ad

Collapse

Announcement

Collapse
No announcement yet.
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • 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

  • #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


    • #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


      • #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

        • seqadmin
          Best Practices for Single-Cell Sequencing Analysis
          by seqadmin



          While isolating and preparing single cells for sequencing was historically the bottleneck, recent technological advancements have shifted the challenge to data analysis. This highlights the rapidly evolving nature of single-cell sequencing. The inherent complexity of single-cell analysis has intensified with the surge in data volume and the incorporation of diverse and more complex datasets. This article explores the challenges in analysis, examines common pitfalls, offers...
          Today, 07:15 AM
        • seqadmin
          Latest Developments in Precision Medicine
          by seqadmin



          Technological advances have led to drastic improvements in the field of precision medicine, enabling more personalized approaches to treatment. This article explores four leading groups that are overcoming many of the challenges of genomic profiling and precision medicine through their innovative platforms and technologies.

          Somatic Genomics
          “We have such a tremendous amount of genetic diversity that exists within each of us, and not just between us as individuals,”...
          05-24-2024, 01:16 PM

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by seqadmin, Today, 08:18 AM
        0 responses
        10 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, Today, 08:04 AM
        0 responses
        12 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, 06-03-2024, 06:55 AM
        0 responses
        13 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, 05-30-2024, 03:16 PM
        0 responses
        27 views
        0 likes
        Last Post seqadmin  
        Working...
        X