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  • © 2019

Genomic Applications in Pathology

  • Review the scientific principles underlying next generation genomic technologies and required bioinformatics approaches.

  • Presents implementation roadmaps for various single gene, gene panels, whole exome and whole genome assays.

  • Written by experts in this field.

  • Provides practice recommendations and guidelines in genomic testing specific to diseases and tumor types.

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Table of contents (39 chapters)

  1. Front Matter

    Pages i-xx
  2. Genomic Technologies

    1. Front Matter

      Pages 1-1
    2. Emerging Next-Generation Sequencing Technologies

      • Matthew W. Anderson
      Pages 23-31
    3. Transcriptome Sequencing (RNA-Seq)

      • Jacquelyn Reuther, Angshumoy Roy, Federico A. Monzon
      Pages 33-49
    4. miRNA Expression Assays

      • Cornelia Braicu, Diana Gulei, Beatriz de Melo Maia, Ioana Berindan-Neagoe, George A. Calin
      Pages 51-71
    5. Circulating Tumor Cells: Enrichment and Genomic Applications

      • Dorraya El-Ashry, Marija Balic, Richard J. Cote
      Pages 73-87
    6. Circulating Cell-Free DNA for Molecular Diagnostics and Therapeutic Monitoring

      • Natasha B. Hunter, Julia A. Beaver, Ben Ho Park
      Pages 89-99
  3. Practice-Related Aspects of Clinical Genomics

    1. Front Matter

      Pages 101-101
    2. Genomic Pathology: Training for New Technology

      • Richard L. Haspel
      Pages 103-111
    3. Patents and Proprietary Assays

      • Roger D. Klein
      Pages 127-134
    4. Ethical Issues in Clinical Genetics and Genomics

      • Henry T. Greely
      Pages 135-146
  4. Clinical Implementation of Diagnostic Genomics

    1. Front Matter

      Pages 147-147
    2. Bioinformatics Tools in Clinical Genomics

      • David K. Crockett, Karl V. Voelkerding, Alan F. Brown, Rachel L. Stewart
      Pages 163-182
    3. Next-Generation Sequencing for Single-Gene Analysis

      • Hao Ho, Christopher D. Gocke
      Pages 183-190
    4. Next-Generation Sequencing for Gene Panels

      • Michael O. Dorschner
      Pages 191-202

About this book

  ​The recent advances in genomics are continuing to reshape our approach to diagnostics, prognostics and therapeutics in oncologic and other disorders. A paradigm shift in pharmacogenomics and in the diagnosis of genetic inherited diseases and infectious diseases is unfolding as the result of implementation of next generation genomic technologies. With rapidly growing knowledge and applications driving this revolution, along with significant technologic and cost changes, genomic approaches are becoming the primary methods in many laboratories and for many diseases.

  As a result, a plethora of clinical genomic applications have been implemented in diagnostic pathology laboratories, and the applications and demands continue to evolve rapidly. This has created a tremendous need for a comprehensive resource on genomic applications in clinical and anatomic pathology. We believe that our current textbook provides such a resource to practicing molecular pathologists, hematopathologists and other subspecialized pathologists, general pathologists, pathology and other trainees, oncologists, geneticists and a growing spectrum of other clinicians.  With periodic updates and a sufficiently rapid time from submission to publication, this textbook will be the resource of choice for many professionals and teaching programs. Its focus on genomics parallels the evolution of these technologies as primary methods in the clinical lab. The rapid evolution of genomics and its applications in medicine necessitates the (frequent) updating of this publication.

This text will provide a state-of-the art review of the scientific principles underlying next generation genomic technologies and the required bioinformatics approaches to analyses of the daunting amount of data generated by current and emerging genomic technologies. Implementation roadmaps for various clinical assays such as single gene, gene panels, whole exome and whole genome assays will be discussed together with issues related to reporting and the pathologist’s role in interpretation and clinical integration of genomic tests results. Genomic applications for site-specific solid tumors and hematologic neoplasms will be detailed. Genomic applications in pharmacogenomics, inherited genetic diseases and infectious diseases will also be discussed. The latest iteration of practice recommendations or guidelines in genomic testing put forth by stakeholder professional organizations such as the College of American Pathology and the Association for Molecular Pathology, will be discussed as well as regulatory issues and laboratory accreditation related to genomic testing. All chapters will be written by experts in their fields and will include the most up to date scientific and clinical information.   



Reviews

“This is a great book for pathologists who are looking for a comprehensive review of genomic pathology. The book discusses in detail the emerging genomic modalities, addresses practical issues related to the implementation of genomic testing, and gives a full account of the use of genomic testing in various diseases. The authors do a good job of balancing the generally accepted understanding of genomic pathology and its interpretation based on years of experience in the field. Overall, I highly recommend this book.” (Grace Wang, Doody's Book Reviews, April, 2019)

Editors and Affiliations

  • Professor and Chair of Pathology, University of Alabama at Birmingham, Birmingham, USA

    George Jabboure Netto

  • Department of Pathology and Laboratory Medicine, NorthShore University HealthSystem, Clinical Professor of Pathology, University of Chicago Pritzker School of Medicine, Evanston, USA

    Karen L. Kaul

About the editors

George J. Netto
University of Alabama at Birmingham
Birmingham, AL
USA

Karen L. Kaul
NorthShore University HealthSystem
University of Chicago Pritzker School of Medicine
Evanston, IL
USA

Bibliographic Information

  • Book Title: Genomic Applications in Pathology

  • Editors: George Jabboure Netto, Karen L. Kaul

  • DOI: https://doi.org/10.1007/978-3-319-96830-8

  • Publisher: Springer Cham

  • eBook Packages: Medicine, Medicine (R0)

  • Copyright Information: Springer International Publishing AG, part of Springer Nature 2019

  • Hardcover ISBN: 978-3-319-96829-2Published: 21 December 2018

  • eBook ISBN: 978-3-319-96830-8Published: 10 December 2018

  • Edition Number: 2

  • Number of Pages: XX, 638

  • Number of Illustrations: 8 b/w illustrations, 108 illustrations in colour

  • Topics: Pathology, Oncology, Laboratory Medicine, Human Genetics

Buy it now

Buying options

eBook USD 189.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Hardcover Book USD 249.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Other ways to access