An edition of Clinical bioinformatics (2007)

Clinical bioinformatics

Second Edition.
Clinical bioinformatics
R. J. Trent, R. J. Trent
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Last edited by MARC Bot
December 8, 2022 | History
An edition of Clinical bioinformatics (2007)

Clinical bioinformatics

Second Edition.

This edition doesn't have a description yet. Can you add one?

Publish Date
Publisher
Humana Press
Language
English
Pages
326

Buy this book

Previews available in: English

Edition Availability
Cover of: Clinical bioinformatics
Clinical bioinformatics
2014, Humana Press
in English - Second Edition.
Cover of: Clinical bioinformatics
Clinical bioinformatics
2007, Humana, Springer [distributor], Springer distributor
in English

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Book Details


Table of Contents

From the phenotype to the genotype via bioinformatics / Cali E. Willet and Calire M. Wade
Production and analytic bioinformatics for next-generation DNA sequencing / Richard James, Nigel Allcock
Analyzing the metabolome / Fracnis G. Bowling and Mervyn Thomas
Statistical perspectives for Genome-Wide Association Studies (GWAS) / Jennifer H. Barrett, John C. Taylor, and Mark M. Iles
Bioinformatics challenges in Genome-Wide Association Studies (GWAS) / Rishika De, William S. Bush, and Jason H. Morre
Studying cancer genomics through next-generation DNA sequencing and bioinformatics / Maraia A. Doyle, Jason LI, Ken Doig, Andrew Fellowes, and Stephen Q. Wong - Using bioinformatics tools to study the role of microRNA in cancer / Fabio Passetti, Natasha Andressa Noguiera Jorge, and Alan Durham
Chromosome microarrays in diagnostic testing : interpreting the genomic data / Greg B. Peters and Mark D. Pertile
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
Pathogen genome bioinformatics / Vitali Sintchenko and Michael P.V. Roper
Setting up next-generation sequencing in the medical laboratory / Bing Yu
Managing Incidental findings in Exome sequencing for research / Marcus J. Hinch cliffe
Approaches for classifying DNA variants found by Sanger sequencing in Medical Genetics Laboratory / Pak Leng Cheong and Melody Caramins
Designing algorithms for determining significance of DNA Missense changes / Sivakumar Gowrisankar and Matthew S. Lebo
DNA variant databases : current state and future directions / John-Paul Plazzer and Finalay Macrae
Natural language processing in biomedecine : a unified system architecture overview / Son Doan, Mike Conway, Tu Minh Phuong, and Lucila Ohno-Machado
Candidate gene discovery and prioritization in rare diseases / Anil G. Jegga
Computer-aided drug designing / Mohini Gore and Neetin S. Desai.

Edition Notes

Published in
New York
Series
Methods in molecular medicine -- 1168

Classifications

Library of Congress
QH324.2 .C556 2014, QH324.2-324.25

The Physical Object

Pagination
xi, 326 pages
Number of pages
326

ID Numbers

Open Library
OL30388980M
ISBN 10
1493908464, 1493908472
ISBN 13
9781493908462, 9781493908479
LCCN
2014939636
OCLC/WorldCat
880899899

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History

Download catalog record: RDF / JSON / OPDS | Wikipedia citation
December 8, 2022 Edited by MARC Bot import existing book
February 26, 2022 Edited by ImportBot import existing book
September 21, 2020 Created by MARC Bot Imported from Library of Congress MARC record