Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • Mimmy86
    Junior Member
    • Oct 2013
    • 3

    #1

    Bisulfite seq format file, help!

    Hi everyone,
    I'm new in methylation analysis and I downloaded a public bisulfite seq data, but I cannot tell what the file format is .
    The file ends in a bs-call.basecall.

    The file contents is:
    chr1 131398 CC 12 0 -
    chr1 131399 CC 12 0 -
    chr1 131400 CC 13 0 +
    chr1 131401 CC 13 0 +
    chr1 131402 CG 2 11 +
    chr1 131403 CG 4 10 -
    chr1 131404 CA 13 0 +
    chr1 131407 CC 13 0 +
    chr1 131408 CC 13 0 +
    chr1 131409 CC 15 0 +
    chr1 131410 CA 15 0 +
    chr1 131412 CA 15 0 +


    Do you know this kind of file?

    Thank a lot!!!!!
    Mimmy
    Last edited by Mimmy86; 10-25-2013, 07:20 AM.
  • dpryan
    Devon Ryan
    • Jul 2011
    • 3478

    #2
    It would help if you gave a URL. Particularly if this is a GEO dataset, there's probably a description somewhere. Having said that, it looks like: chromosome, position, context, unmethylated count, methylated count, strand. Context gives the nucleotide position following the C in question (these days, you'd see CpG, CHG, or CHH rather than what you have).

    Comment

    • GenoMax
      Senior Member
      • Feb 2008
      • 7142

      #3
      From this GEO record: http://www.ncbi.nlm.nih.gov/geo/quer...?acc=GSM922329 comes following tidbit

      Supplementary_files_format_and_content: Methylation calls files for C's in the bsmap alignment files were generated using methratio.py
      Seems to be similar to what Mimmy86 is reporting.

      Comment

      • Mimmy86
        Junior Member
        • Oct 2013
        • 3

        #4
        Hi,
        thaks for your replay!
        As you said i took this data from GEO GSM922329.
        I examined methratio.py manual in bsmap and I find an output file description that confused me.
        The description is
        Output format: tab delimited txt file with the following columns:
        1) chromorome
        2) coordinate (1-based)
        3) strand
        4) sequence context (2nt upstream to 2nt downstream in Watson strand direction)
        5) methylation ratio, calculated as #C_counts / #eff_CT_counts
        6) number of effective total C+T counts on this locus (#eff_CT_counts)
        CT_SNP="no action", #eff_CT_counts = #CT_counts
        CT_SNP="correct", #eff_CT_counts = #CT_counts * (#rev_G_counts / #rev_GA_counts)
        7) number of total C counts on this locus (#C_counts)
        8) number of total C+T counts on this locuso (#CT_counts)
        9) number of total G counts on this locus of reverse strand (#rev_G_counts)
        10) number of total G+A counts on this locus of reverse strand (#rev_GA_counts)
        11) lower bound of 95% confidence interval of methylation ratio, calculated by Wilson score interval for binomial proportion.
        12) upper bound of 95% confidence interval of methylation ratio, calculated by Wilson score interval for binomial proportion.

        Comment

        • fkrueger
          Senior Member
          • Sep 2009
          • 627

          #5
          If the description on GEO (...produced by methratio.py) and the actual format are not matching you should probably contact the authors directly (also so that they can update the description on GEO). Looking at the file I am pretty sure though that Devon's assessment is correct.

          Comment

          • Mimmy86
            Junior Member
            • Oct 2013
            • 3

            #6
            thanks, I also think that Devon's assessment is correct. I tried to calculate the Cmethylation frequency using the 4th and 5th columns. do you think that i can continue on this frequencies?

            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, 08-13-2026, 12:22 PM
            0 responses
            28 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 08-11-2026, 10:35 AM
            0 responses
            22 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 08-06-2026, 07:41 AM
            0 responses
            37 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 08-03-2026, 10:13 AM
            0 responses
            51 views
            0 reactions
            Last Post SEQadmin2  
            Working...