Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • karve
    Member
    • Feb 2011
    • 12

    Doing things with CrossBow output ?

    I've used CrossBow ( took 3 hours on a 3 node, 10 core Hadoop cluster ) and worked through the mouse, chromosome 17 example given in the manual successfully to the end.. I now have 276,819 SNPs in SoapSNP output format and all the intermediate files..

    I want to view this stuff graphically - zooming in, exploding it, seeing if they cluster in certain areas etc - sort of like what the original paper http://genomebiology.com/2009/10/10/R112 does.

    I think I'm looking for a graphical display tool - something that can take in the reference sequence of the mouse chromosome 17 (all 95 million bases of it), the SNP calls( all 276K of them ) that Crossbow produced in SoapSNP output format and then let me look at it visually.

    A tool that could marry the two to produce a new sequence, substituting the SNPs at the relevant points would be nice too.

    Is this asking too much ? I've seen some fancy graphical tools at the EBI and NCBI websites so they have to be there, surely? Any ideas ?
  • KevinLam
    Senior Member
    • Nov 2009
    • 204

    #2
    You may wish to check out IGV for the BAM file for the visualization. using the SNp lists like a directory/index

    for others you can see

    Pubmed Link Bioinformatics. 2011 Jan 28. [Epub ahead of print] Bambino: a variant detector and alignment viewer for next-generation sequenc...
    http://kevin-gattaca.blogspot.com/

    Comment

    • karve
      Member
      • Feb 2011
      • 12

      #3
      Thanks - I executed the 10 min. IGV tutorial. There's a LOT to that software isn't there. Checking out Bambino as well.

      Comment

      • karve
        Member
        • Feb 2011
        • 12

        #4
        Well I've scanned a whole set of visualizer products ( IGV, JMAPViewer, conversion tools ) to see if I can visualize the output of CrossBow out of the box so to speak. No success yet - seems like the output format of CrossBow is rather specific.. The description of it is at the bottom of this post. I just can't seem to find a tool that will convert it to a format that a visualizer will use, or a visualizer that will display that format out of the box. Am I missing something here ? Just checking before I start writing some code to do the conversions to a visualizer compatible format myself.


        ======================================
        Each individual record is in the SOAPsnp output format. SOAPsnp's format consists of 1 SNP per line with several tab-separated fields per SNP. The fields are:

        1. Chromosome ID
        2. 1-based offset into chromosome
        3. Reference genotype
        4. Subject genotype
        5. Quality score of subject genotype
        6. Best base
        7. Average quality score of best base
        8. Count of uniquely aligned reads corroborating the best base
        9. Count of all aligned reads corroborating the best base
        10. Second best base
        11. Average quality score of second best base
        12. Count of uniquely aligned reads corroborating second best base
        13. Count of all aligned reads corroborating second best base
        14. Overall sequencing depth at the site
        15. Sequencing depth of just the paired alignments at the site
        16. Rank sum test P-value
        17. Average copy number of nearby region
        18. Whether the site is a known SNP from the file specified with -s
        =================================

        Comment

        • karve
          Member
          • Feb 2011
          • 12

          #5
          Well, I've looked at a lot of genome browsers of varying pedigree. JMapViewer came closest in allowed me to look at the SNP file, in SOAPsnp format visually.. out of the box. It also wanted an alignment file, in Soap(Aligner) output format so I had to fake that and if I had access to the source code...

          No joy anywhere else.

          So I'm resigned to doing the conversions as needed, to VFC, BED, whichever formats are required by the software. From that perspective, the richness, pedigree and existing data availability ( annotation tracks ) of the genome browsers of the really large orgs look very good - I mean the UCSC Genome Browser, the Broad Institute's IGV and the NCBI MAP Viewer look good. That they make the source available is also good.

          I did have a problem with the IGV with mouse mm9, chr17 SNPs. when "loading from server", the SNP128 ( and also the repeats ) annotation tracks, it came back with

          An error occurred while loading igvdata.broadinstitute.org/annotations/mm9/variations/snp128.bed.gz data
          Error parsing header.


          Pity. No such problems with hg19 though - and looking at the file-names when it works (hg19) v when it doesn't(mm9), the .gz is a difference I note.

          The UCSC Genome Browser had no problems displaying their known versions of the SNPs.

          1. Now if anybody can explain to me where chromosome ideogram band labels/names come from ? There's a naming convention there, in those p13.2, q21.32 labels right ? google doesn't answer a simple question like that.

          EDIT: looks like the personal Genome SNP format ( PGSNP ) for an upload of a custom annotation track is now available on the main UCSC genome browser, not just the test one.. as per an archived message from them in the mailing list.
          Last edited by karve; 03-08-2011, 09:24 AM. Reason: mention PGSNP format

          Comment

          Latest Articles

          Collapse

          • 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
          • SEQadmin2
            Advanced Sequencing Platforms Tackle Neuroscience’s Toughest Genomics Problems
            by SEQadmin2



            Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
            ...
            07-09-2026, 11:10 AM
          • SEQadmin2
            Cancer Drug Resistance: The Lingering Barrier to Rising Survival
            by SEQadmin2



            Cancer survival rates have significantly increased in the last few decades in the United States, reaching a combined 70% 5-year survival rate by 2021. Behind this number, there are years of research to find new therapies, drug targets, and early detection methods. But there is one core challenge that keeps slowing down these advances, and it’s about drug resistance.

            There is no single reason why many patients don’t respond to treatment as expected. Cancer is...
            07-08-2026, 05:17 AM

          ad_right_rmr

          Collapse

          News

          Collapse

          Topics Statistics Last Post
          Started by SEQadmin2, 07-24-2026, 12:17 PM
          0 responses
          21 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 07-23-2026, 11:41 AM
          0 responses
          19 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 07-20-2026, 11:10 AM
          0 responses
          26 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 07-13-2026, 10:26 AM
          0 responses
          38 views
          0 reactions
          Last Post SEQadmin2  
          Working...