Book Volume 6620 2012

Bioinformatics for Personalized Medicine

10th Spanish Symposium, JBI 2010, Torremolinos, Spain, October 27-29, 2010. Revised Selected Papers


ISBN: 978-3-642-28061-0 (Print) 978-3-642-28062-7 (Online)

Table of contents (13 chapters)

  1. Front Matter

    Pages -

  2. Chapter

    Pages 1-7

    Statistical Significance for NGS Reads Similarities

  3. Chapter

    Pages 8-20

    Application of Array-Oriented Scientific Data Formats (NetCDF) to Genotype Data, GWASpi as an Example

  4. Chapter

    Pages 21-28

    An Ontology and a REST API for Sequence Based Microbial Typing Data

  5. Chapter

    Pages 29-41

    Multivariate Methods for the Integration and Visualization of Omics Data

  6. Chapter

    Pages 42-49

    A Holistic Approach for Integrating Genomic Variation Information

  7. Chapter

    Pages 50-65

    SB-KOM: Integration of Pathway Information with BioPax

  8. Chapter

    Pages 66-71

    GENote v.β: A Web Tool Prototype for Annotation of Unfinished Sequences in Non-model Eukaryotes

  9. Chapter

    Pages 72-82

    Interface Similarity Improves Comparison of DNA-Binding Proteins: The Homeobox Example

  10. Chapter

    Pages 83-88

    Pyicos: A Flexible Tool Library for Analyzing Protein-Nucleotide Interactions with Mapped Reads from Deep Sequencing

  11. Chapter

    Pages 89-93

    Novel Angiogenic Functional Targets Predicted through “Dark Matter” Assessment in Protein Networks

  12. Chapter

    Pages 94-101

    jORCA and Magallanes Sailing Together towards Integration of Web Services

  13. Chapter

    Pages 102-107

    iHOP Web Services Family

  14. Chapter

    Pages 108-120

    Bioinformatic Software Developments in Spain

  15. Back Matter

    Pages -