Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • yjhua2110
    Member
    • Nov 2009
    • 68

    #1

    deepBase: a database for annotating and discovering ncRNAs from deep sequencing data

    Dear All,

    We introduce a novel platform/database, deepBase, which we have developed to map, store, retrieve, annotate, integrate and visualize deep sequencing-derived small RNAs, and facilitate transcriptomic research and the discovery of novel ncRNAs.

    deepBase: a database for deeply annotating and mining deep sequencing data. Nucleic Acids Res., 2010,38: D123-D130. December 4, 2009.
    http://nar.oxfordjournals.org/cgi/content/full/gkp943

    deepBase is available at: http://deepbase.sysu.edu.cn/

    Features of deepBase as follows,
    Deep sequencing data and species
    Deep sequencing data from 185 (now is 237) small RNA libraries from diverse tissues and cell lines.
    Seven organisms: human, mouse, chicken, Ciona intestinalis, Drosophila melanogaster, Caenhorhabditis elegans and Arabidopsis thaliana.
    Annotation and identification of diverse small RNAs
    we annotated and identified
    ~380 000 unique ncRNA-associated small RNAs (nasRNAs)
    ~1.5 million unique promoter-associated small RNAs (pasRNAs)
    ~4.0 million unique exon-associated small RNAs (easRNAs)
    ~6 million unique repeat-associated small RNAs (rasRNAs)
    Discovering RNA clusters and long ncRNAs
    We identified
    about 1.2 million RNA clusters that include multiple classes of infrastructural ncRNAs (e.g. tRNAs, rRNAs, snRNA and snoRNAs), miRNAs precursor, piRNA precursors, repeat-associated siRNA precursors and evolutionarily conserved phastCons elements.
    ~2000 microRNA candidates were identified from deep sequencing data using modified miRDeep program.
    ~1890 snoRNA candidates were predicted from RNA clusters using our snoSeeker program.
    Visualization
    A new visualization tool, deepView genome browser, to provide an integrated view of mapped reads, known and predicted ncRNAs, protein-coding genes and RNA clusters and their expression peaks (mapped small RNA density).
    Stand-alone graphical interface (GUI) tools
    Stand-alone graphical user interface (GUI) tools for deep sequencing-derived small RNA were provided in deepBase. All these softwares are preliminary version. We are actively updating and maintaining them.

    This is the first version of deepBase database. We look forward to your feedback.

    Thanks!
    JianHua
    Last edited by yjhua2110; 11-04-2010, 04:41 AM.
  • yjhua2110
    Member
    • Nov 2009
    • 68

    #2
    We are integrating published next-generation small RNA-Seq datasets to our deepBase data. And we hope you contribute your next-generation small RNA-Seq datasets to our deepBase.

    For more information see the deepBase submission page


    Thank you very much!

    Comment

    • yjhua2110
      Member
      • Nov 2009
      • 68

      #3
      mapped reads associated with known microRNAs

      We also have mapped reads from deep-sequencing experiments to known microRNAs downloaded from miRBase and developed a variety of interfaces and graphical visualization to view these mapped reads. You can retrieve a list of microRNAs and list of variants and their read counts and isomiRs...

      Web interfaces to view mapped reads associated with known microRNAs as follows:
      (1) http://deepbase.sysu.edu.cn/browseNasRNA.php
      (2) http://deepbase.sysu.edu.cn/browseExpress.php
      Last edited by yjhua2110; 11-04-2010, 04:51 AM.

      Comment

      • yjhua2110
        Member
        • Nov 2009
        • 68

        #4
        heatmap (microRNA and ncRNA expression pattern)

        We have updated the heatmap (microRNA and ncRNA expression pattern) generated from mapped deep-sequencing reads.

        web interface to view heatmap as follows:


        Last edited by yjhua2110; 11-04-2010, 04:51 AM.

        Comment

        • yjhua2110
          Member
          • Nov 2009
          • 68

          #5
          snoSeekerNGS: Discovering snoRNAs from pooled deep-sequencing data

          We had released a software package, snoSeekerNGS, for discovering snoRNAs from pooled deep sequencing data.

          SnoSeekerNGS is freely available from the following URL: http://deepbase.sysu.edu.cn/SnoSeekerNGS.php. Choose the appropriate platform for a binary distribution or a graphical user interface (GUI) distribution.
          Last edited by yjhua2110; 11-30-2010, 12:15 AM.

          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, 08-03-2026, 10:13 AM
          0 responses
          15 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 07-31-2026, 02:55 AM
          0 responses
          32 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 07-24-2026, 12:17 PM
          0 responses
          23 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 07-23-2026, 11:41 AM
          0 responses
          21 views
          0 reactions
          Last Post SEQadmin2  
          Working...