Description

Book Synopsis

In Clinical Bioinformatics, Second Edition, leading experts in the field provide a series of articles focusing on software applications used to translate information into outcomes of clinical relevance.



Table of Contents

1. From the Phenotype to the Genotype via Bioinformatics

Cali E. Willet and Claire M. Wade

2. Production and Analytic Bioinformatics for Next-Generation DNA Sequencing

Richard James Nigel Allcock

3. Analyzing the Metabolome

Francis G. Bowling and Mervyn Thomas

4. Statistical Perspectives for Genome-Wide Association Studies (GWAS)

Jennifer H. Barrett, John C. Taylor and Mark M. Iles

5. Bioinformatics Challenges in Genome-Wide Association Studies (GWAS)

Rishika De, William S. Bush, and Jason H. Moore

6. Studying Cancer Genomics through Next-Generation Sequencing and Bioinformatics

Maria A. Doyle, Jason Li, Ken Doig, Andrew Fellowes, and Stephen Q. Wong

7. Using Bioinformatics Tools to Study the Role of microRNA in Cancer

Fabio Passetti, Natasha Jorge, and Alan Durham

8. Chromosome Microarrays in Diagnostic Testing: Interpreting the Genomic Data

Greg B. Peters and Mark D. Pertile

9. Bioinformatics Approach to Understanding Interacting Pathways in Neuropsychiatric Disorders

Ali Alawieh, Zahraa Sabra, Amaly Nokkari, Atlal El-Assaad, Stefania Mondello, Fadi Zaraket, Bilal Fadlallah, and Firas H. Kobeissy

10. Pathogen Genome Bioinformatics

Vitali Sintchenko and Michael P.V. Roper

11. Setting Up Next-Generation DNA Sequencing in the Medical Laboratory

Bing Yu

12. Managing Incidental Findings in Exome Sequencing for Research

Marcus J. Hinchcliffe

13. Approaches for Classifying DNA Variants Found by Sanger Sequencing in a Medical Genetics Laboratory

Pak Leng Cheong and Melody Caramins

14. Designing Algorithms for Determining Significance of DNA Missense Changes

Sivakumar Gowrisankar and Matthew S. Lebo

15. DNA Variant Databases: Current and Future Directions

John-Paul Plazzer and Finlay Macrae

16. Natural Language Processing Systems in Biomedicine: A Unified System Architecture Overview

Son Doan, Mike Conway, Tu Minh Phuong, and Lucila Ohno-Machado

17. Candidate Gene Discovery and Prioritization in Rare Diseases

Anil G. Jegga

18. Computer Aided Drug Designing

Mohini Gore and Neetin S. Desai

Clinical Bioinformatics 2014

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    A Hardback by Ronald Trent

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      Publisher: Humana Press Inc.
      Publication Date: Publication Date: 28/05/2014
      ISBN13: 9781493908462, 978-1493908462
      ISBN10: 1493908464

      Description

      Book Synopsis

      In Clinical Bioinformatics, Second Edition, leading experts in the field provide a series of articles focusing on software applications used to translate information into outcomes of clinical relevance.



      Table of Contents

      1. From the Phenotype to the Genotype via Bioinformatics

      Cali E. Willet and Claire M. Wade

      2. Production and Analytic Bioinformatics for Next-Generation DNA Sequencing

      Richard James Nigel Allcock

      3. Analyzing the Metabolome

      Francis G. Bowling and Mervyn Thomas

      4. Statistical Perspectives for Genome-Wide Association Studies (GWAS)

      Jennifer H. Barrett, John C. Taylor and Mark M. Iles

      5. Bioinformatics Challenges in Genome-Wide Association Studies (GWAS)

      Rishika De, William S. Bush, and Jason H. Moore

      6. Studying Cancer Genomics through Next-Generation Sequencing and Bioinformatics

      Maria A. Doyle, Jason Li, Ken Doig, Andrew Fellowes, and Stephen Q. Wong

      7. Using Bioinformatics Tools to Study the Role of microRNA in Cancer

      Fabio Passetti, Natasha Jorge, and Alan Durham

      8. Chromosome Microarrays in Diagnostic Testing: Interpreting the Genomic Data

      Greg B. Peters and Mark D. Pertile

      9. Bioinformatics Approach to Understanding Interacting Pathways in Neuropsychiatric Disorders

      Ali Alawieh, Zahraa Sabra, Amaly Nokkari, Atlal El-Assaad, Stefania Mondello, Fadi Zaraket, Bilal Fadlallah, and Firas H. Kobeissy

      10. Pathogen Genome Bioinformatics

      Vitali Sintchenko and Michael P.V. Roper

      11. Setting Up Next-Generation DNA Sequencing in the Medical Laboratory

      Bing Yu

      12. Managing Incidental Findings in Exome Sequencing for Research

      Marcus J. Hinchcliffe

      13. Approaches for Classifying DNA Variants Found by Sanger Sequencing in a Medical Genetics Laboratory

      Pak Leng Cheong and Melody Caramins

      14. Designing Algorithms for Determining Significance of DNA Missense Changes

      Sivakumar Gowrisankar and Matthew S. Lebo

      15. DNA Variant Databases: Current and Future Directions

      John-Paul Plazzer and Finlay Macrae

      16. Natural Language Processing Systems in Biomedicine: A Unified System Architecture Overview

      Son Doan, Mike Conway, Tu Minh Phuong, and Lucila Ohno-Machado

      17. Candidate Gene Discovery and Prioritization in Rare Diseases

      Anil G. Jegga

      18. Computer Aided Drug Designing

      Mohini Gore and Neetin S. Desai

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