Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • dwb0211
    Member
    • Nov 2008
    • 11

    #1

    how to get target gene from BED format

    Recently I download the BED file from GEO, the authors used ChIP-Seq to find the ERa bing site genome-wide,but just supply the peak, the question is how to find the likely regulated target genes from these peaks?

    here is the format:

    Code:
    track name=ER_E2 description=ER_E2
    chr1	557112	558114
    chr1	559459	560286
    chr1	998864	999397
    chr1	999399	999604
    chr1	1004343	1005146
    chr1	1070346	1071080
    chr1	1305474	1306502
    chr1	1358287	1358744
    chr1	1776987	1777750
    chr1	1820476	1821168
    chr1	1922754	1923628
    chr1	2131962	2132747
    chr1	2325805	2326447
    chr1	2368996	2369977
    ....
    when I load all these data in UCSC,there is a error happend,and puzzled me.

    Could someone give me some clue convert these bing-sites to target genes?

    I know some R language but no idea completely.



    here is the website:ftp://ftp.ncbi.nih.gov/pub/geo/DATA/...2_peaks.bed.gz



    thx!
  • What_Da_Seq
    Member
    • Jul 2008
    • 28

    #2
    cisgenome has a bunch of useful executables (windows exe and LINUX binaries) and I suggest this one
    refgene_getnearestgene

    Comment

    • dwb0211
      Member
      • Nov 2008
      • 11

      #3
      thank you for your reply very much,

      I used cisgenome for some time,
      when i used the tool to 'file format convert--> bed to cod',there is no result but just a flash of command line.I think there could be some problem come from the Bed file,which confuse me much.

      could somebody shed some light for me? thx very much

      Comment

      • What_Da_Seq
        Member
        • Jul 2008
        • 28

        #4
        Just ad a "rank#" column to the beginning and label the next columns "chromosome" "start" "end" If you do not have more than 1.05 Mio rows you can doe it easily in Excel.
        This is essentially a cod file format. good luck

        Comment

        Latest Articles

        Collapse

        • SEQadmin2
          Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
          by SEQadmin2



          CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).

          Despite this, “CRISPR helped turn genome editing from a specialized technique into
          ...
          07-31-2026, 11:01 AM
        • SEQadmin2
          Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
          by SEQadmin2


          Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

          The systematic characterization of the human proteome has
          ...
          07-20-2026, 11:48 AM

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by SEQadmin2, Yesterday, 10:35 AM
        0 responses
        7 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 08-06-2026, 07:41 AM
        0 responses
        24 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 08-03-2026, 10:13 AM
        0 responses
        43 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 07-31-2026, 02:55 AM
        0 responses
        48 views
        0 reactions
        Last Post SEQadmin2  
        Working...