Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • iqc
    Junior Member
    • Aug 2009
    • 1

    #1

    public paire end (mate pair) transcriptome data set?

    Hi All,

    Does anyone know a public data set that has paired-ends (mate pair) and is on the transcriptome? If I browse a public database such as the NCBI short reads, how can I find out whether a data set has paired ends? Are there other public databases to look?

    Thanks,

    xq
  • ramouz87
    Member
    • Oct 2009
    • 35

    #2
    Originally posted by iqc View Post
    Hi All,

    Does anyone know a public data set that has paired-ends (mate pair) and is on the transcriptome? If I browse a public database such as the NCBI short reads, how can I find out whether a data set has paired ends? Are there other public databases to look?

    Thanks,

    xq
    Hi xq,
    have you find such dataset ? I looking for that too.
    i would be thankfull if you could let me know
    thanks uin advance,
    Regards,
    Ramzi
    Research Scientist - Bioinformatics
    Sidra Medical and Research Center

    Comment

    • Chien-Yuan Chen
      Member
      • Feb 2009
      • 19

      #3
      GEO data GSE 13652
      Expression profiling by high throughput sequencing
      We carried out the first analysis of alternative splicing complexity in human tissues using mRNA-Seq data. New splice junctions were detected in 20% of multiexon genes, many of which are tissue specific. By combining mRNA-Seq and EST-cDNA sequence data, we estimate that transcripts from 95% of multiexon genes undergo alternative splicing and that there are 100,000 intermediate- to high-abundance alternative splicing events in major human tissues. From a comparison with quantitative alternative splicing microarray profiling data, we also show that mRNA-Seq data provide reliable measurements for exon inclusion levels.

      Keywords: mRNA expression


      Overall design 32-nucleotide sequence reads from six human tissues including brain, cerebral cortex, heart, liver, lung and skeletal muscle.


      Contributor(s) Pan Q, Shai O, Lee LJ, Frey BJ, Blencowe BJ
      Citation(s) 18978789
      Pan Q, Shai O, Lee LJ, Frey BJ et al. Deep surveying of alternative splicing complexity in the human transcriptome by high-throughput sequencing. Nat Genet 2008 Dec;40(12):1413-5. PMID: 18978789

      Submission date Nov 18, 2008
      Contact name Weijun Gao
      Organization name University of Toronto

      Street address 10 King's College Rd.

      City Toronto
      ZIP/Postal code M5S 3G4
      Country Canada

      Platforms (1) GPL9052 Illumina Genome Analyzer (Homo sapiens)

      Samples (6)
      Less...
      More... GSM343511 brain
      GSM343512 cerebral cortex
      GSM343513 heart

      GSM343514 liver
      GSM343515 lung
      GSM343516 skeletal muscle


      Download family Format
      SOFT formatted family file(s) SOFT
      MINiML formatted family file(s) MINiML
      Series Matrix File(s) TXT

      Supplementary file Size Download File type/resource
      GSE13652_RAW.tar 2.7 Gb (ftp)(http) TAR (of TXT)
      SRP000/SRP000626 (ftp) SRA Study
      Raw data not provided for this record
      Processed data provided as supplementary file

      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
      • 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

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by SEQadmin2, Today, 07:41 AM
      0 responses
      9 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 08-03-2026, 10:13 AM
      0 responses
      25 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 07-31-2026, 02:55 AM
      0 responses
      38 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 07-24-2026, 12:17 PM
      0 responses
      25 views
      0 reactions
      Last Post SEQadmin2  
      Working...