Persistent
 

Bioinformatics

Researchers require analytic solutions to map experimental data in the context of biological systems for

  • Effective interpretation of high-throughput data
  • Gaining insights into multidimensional data
  • Correlating experimental data with annotation, clinical and administrative data

Integration of disparate sources of biological data to leverage publicly-curated biological content combined with proprietary content sources for

  • Efficient searching, querying and reporting for research
  • Enabling translational research
  • Ensuring data consistency, security and compliance

Persistent Advantage

  • Team of domain experts including a number of experienced molecular biologist, bioinformaticians  with PhDs in bioinformatics, computer science, statistics, and biology
  • Hands-on knowledge of tools including Genespring, Rosetta Resolver, Spotfire, tools for Sanger as well as NGS data analysis
  • Computational Experts having extensive experience with R, Bioconductor, Matlab, SAS, SPSS, Clementine, Intelligent Miner, Octave, Weka, Scilab, Orange
  • Deep understanding of various life sciences and experiment data sources such as Entrez Gene, Unigene, Gene Ontology, Homologene, dbSNP, GEO, ArrayExpress, BIND

Persistent Offerings

  • Sanger and Next Generation Sequencing, Genotyping, Mutation Profiling
    • Data Warehousing for high-throughput sequencing  data
    • Development of new algorithms for secondary and tertiary sequence data analysis
    • Performance improvement of prototype algorithms/tools
    • Development of new tools  for  sequence data visualization, experiment specific pipeline
    • Enhancement and support for exciting software and tools
    • Customize widely used open source sequence analysis tools to support for Next Gen Sequencing (NGS) plate form specific analysis
    • Algorithm/Functional Testing
  • Gene Expression Analysis
    • Gene Expression Analysis Platform with comprehensive statistical analysis and visualization tools
    • Algorithms for correlating annotation data with expression data
    • Visualization: Bar graph, scatter plot and heat-map (all web-based)
  • Proteomics
    • Workflow management
    • Multi-role system
  • Metabolomics
    • Looking for signatures in spectroscopic data
    • Detection of anomalies like spikes, artifacts etc.
  • Data mart design based on
    • Life sciences semantics
    • Reporting requirements for scientific explorations
    • Reusable parsing framework and components for
    • Biological data formats
    • Entrez Gene, Gene Ontology, Homologene, UniGene, dbSNP
    • Domain specific transformation strategies
    • Mapping of multimodality data
    • Annotations: experimental, clinical, chemical, biological
       

 

cancer Biomedical Informatics Grid, caBIG and the caBIG logo are registered trademarks of HHS used in connection with the National Cancer Institute’s caBIG® program

 
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