Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • ips
    Member
    • Jan 2011
    • 11

    #1

    How to handle this dataset?

    Hi all,
    I have upload a txt format NGS data, after that ,under "Change Datatype" set "New Type" to interval and then click "Execute". The dataset I created like this:

    chr10 91346072 91346098 - 2119.5.1 0 ATACTAGAAAACTCTAATGTCCAAAA
    chr15 9879235 9879261 - 2119.5.2 0 AGACAAAACTCACATTCTTTCTATCA
    chr5 45627890 45627916 + 2119.5.3 1 GGGCGGCCCTGGGGATGCTCCCTCCA
    chr18 24025706 24025732 - 2119.5.4 0 CTGGTATATATTAAAAGCCACTCCTC
    This history column did not show "display at UCSC main "
    How can I get visialized in UCSC genome browser?
  • Simon Anders
    Senior Member
    • Feb 2010
    • 995

    #2
    You haven't even told us what application you are talking about.

    Comment

    • ips
      Member
      • Jan 2011
      • 11

      #3
      I want to do Chip-seq analysis for this data.

      Comment

      • RDW
        Member
        • Oct 2008
        • 63

        #4
        Yes, but what software are you trying to use? From the option names, my guess would be Galaxy. Are you able to display other Galaxy data on the UCSC browser, or is the problem just with this file?

        Comment

        • ips
          Member
          • Jan 2011
          • 11

          #5
          I can display other Galaxy data on the UCSC browser.

          Comment

          • ips
            Member
            • Jan 2011
            • 11

            #6
            By the way, the dataset available in http://www.ncbi.nlm.nih.gov/geo/quer...i?acc=GSE12241
            Last edited by ips; 03-21-2011, 01:39 AM.

            Comment

            • nexgengirl
              Member
              • Apr 2010
              • 31

              #7
              Hi,

              To view in the UCSC it should be in the bed format. See this page:


              For you data I think if you follow these steps you should be able to view it in the browser. I just tried it using the lines you provided and it worked so hope this helps.

              1. Make sure you have assigned a database to your dataset. (for example hg18 or hg19)
              2. Since the data is currently separated by spaces and you want it in tab use this tool:
              a. Under Text manipulation click Convert delimiters to TAB. (Convert all: Whitespaces)
              3. Change the datatype of your data to bed
              4. When I did this and clicked display at UCSC main it gave an error because the strand is in the wrong column.
              a. For this I used the Cut tool under Text Manipulation and cut columns (in this order) c1,c2,c3,c7,c5,c4 which correlate with chromosome, start, end, name, score, strand.
              b. I'm not sure which column is your score column so you may do this differently
              5. After these steps I clicked UCSC main view and it displayed

              I really hope this helps!

              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, 10-22-2026, 11:13 AM
              0 responses
              27 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 10-22-2026, 10:48 AM
              0 responses
              20 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
              43 views
              0 reactions
              Last Post SEQadmin2  
              Working...