Table of Contents
Overview of technical aspects and chemistries of next-generation sequencing / Ian S. Hagemann.
Clinical genome sequencing / Tina M. Hambuch, John Mayfield, Shankar Ajay, Michelle Hogue, Carri-Lyn Mead and Erica Ramos.
Targeted hybrid capture methods / Elizabeth C. Chastain.
Amplification-based methods / Marina N. Nikiforova, William A. Laframboise and Yuri E. Nikiforov.
Emerging DNA sequencing technologies / Shashikant Kulkarni and John Pfeifer.
RNA-sequencing and methylome analysis / Shamika Ketkar and Shashikant Kulkarni.
Base calling, read mapping, and coverage analysis / Paul Cliften.
Single nucleotide variant detection using next generation sequencing / David H. Spencer, Bin Zhang and John Pfeifer.
Insertions and deletions (indels) / Jennifer K. Sehn.
Translocation detection using next-generation sequencing / Haley Abel, John Pfeifer and Eric Duncavage.
Copy number variant detection using next-generation sequencing / Alex Nord, Stephen J. Salipante and Colin Pritchard.
Reference databases for disease associations / Wendy S. Rubinstein, Deanna M. Church and Donna R. Maglott.
Reporting of clinical genomics test results / Kristina A. Roberts, Rong Mao, Brendan D. O'Fallon and Elaine Lyon.
Reporting software / Rakesh Nagarajan.
Constitutional diseases: amplification-based next-generation sequencing / Vanessa L. Horner and Madhuri R. Hegde.
Targeted hybrid capture for inherited disease panels / Sami S. Amr and Birgit Funke.
Constitutional disorders: whole exome and whole genome sequencing / Benjamin D. Solomon.
Somatic diseases (cancer): amplification-based next-generation sequencing / Fengqi Chang, Geoffrey L. Liu, Cindy J. Liu and Marilyn M. Li.
Targeted hybrid capture for somatic mutation detection in the clinic / Catherine E. Cottrell, Andrew J. Bredemeyer and Hussam Al-Kateb.
Somatic diseases (cancer): whole exome and whole genome sequencing / Jennifer K. Sehn.
Assay validation / Amy S. Gargis, Lisa Kalman and Ira M. Lubin.
Regulatory considerations related to clinical next generation sequencing / Shashikant Kulkarni and John Pfeifer.
Genomic reference materials for clinical applications / Justin Zook and Marc Salit.
Ethical challenges to next-generation sequencing / Stephanie Solomon.
Legal issues / Roger D. Klein.
Billing and reimbursement / Kris Rickhoff, Andrew Drury and John Pfeifer.
Clinical genome sequencing / Tina M. Hambuch, John Mayfield, Shankar Ajay, Michelle Hogue, Carri-Lyn Mead and Erica Ramos.
Targeted hybrid capture methods / Elizabeth C. Chastain.
Amplification-based methods / Marina N. Nikiforova, William A. Laframboise and Yuri E. Nikiforov.
Emerging DNA sequencing technologies / Shashikant Kulkarni and John Pfeifer.
RNA-sequencing and methylome analysis / Shamika Ketkar and Shashikant Kulkarni.
Base calling, read mapping, and coverage analysis / Paul Cliften.
Single nucleotide variant detection using next generation sequencing / David H. Spencer, Bin Zhang and John Pfeifer.
Insertions and deletions (indels) / Jennifer K. Sehn.
Translocation detection using next-generation sequencing / Haley Abel, John Pfeifer and Eric Duncavage.
Copy number variant detection using next-generation sequencing / Alex Nord, Stephen J. Salipante and Colin Pritchard.
Reference databases for disease associations / Wendy S. Rubinstein, Deanna M. Church and Donna R. Maglott.
Reporting of clinical genomics test results / Kristina A. Roberts, Rong Mao, Brendan D. O'Fallon and Elaine Lyon.
Reporting software / Rakesh Nagarajan.
Constitutional diseases: amplification-based next-generation sequencing / Vanessa L. Horner and Madhuri R. Hegde.
Targeted hybrid capture for inherited disease panels / Sami S. Amr and Birgit Funke.
Constitutional disorders: whole exome and whole genome sequencing / Benjamin D. Solomon.
Somatic diseases (cancer): amplification-based next-generation sequencing / Fengqi Chang, Geoffrey L. Liu, Cindy J. Liu and Marilyn M. Li.
Targeted hybrid capture for somatic mutation detection in the clinic / Catherine E. Cottrell, Andrew J. Bredemeyer and Hussam Al-Kateb.
Somatic diseases (cancer): whole exome and whole genome sequencing / Jennifer K. Sehn.
Assay validation / Amy S. Gargis, Lisa Kalman and Ira M. Lubin.
Regulatory considerations related to clinical next generation sequencing / Shashikant Kulkarni and John Pfeifer.
Genomic reference materials for clinical applications / Justin Zook and Marc Salit.
Ethical challenges to next-generation sequencing / Stephanie Solomon.
Legal issues / Roger D. Klein.
Billing and reimbursement / Kris Rickhoff, Andrew Drury and John Pfeifer.
Kulkarni, Shashikant;Pfeifer, John D
- Elsevier/Academic Press
2015
9780124051737
9780124047488
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