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NextGeners = pedagogical considerati...

Griffith, Bryant.

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NextGeners = pedagogical considerations /

Record Type:	Electronic resources : Monograph/item
Title/Author:	NextGeners/ by Bryant Griffith.
Reminder of title:	pedagogical considerations /
Author:	Griffith, Bryant.
Published:	Rotterdam :SensePublishers : : 2016.,
Description:	xi, 144 p. :ill., digital ;24 cm.
Contained By:	Springer eBooks
Subject:	Generation Y - Education. -
Online resource:	http://dx.doi.org/10.1007/978-94-6300-642-2
ISBN:	9789463006422

NextGeners = pedagogical considerations /
Griffith, Bryant.

NextGenerspedagogical considerations /[electronic resource] :by Bryant Griffith. - Rotterdam :SensePublishers :2016. - xi, 144 p. :ill., digital ;24 cm.

This book covers topics of these applications, including potential limitations and expanded application in the future. To the fast development of a variety of Next Geners technologies in the post human genome project era, sequencing analysis of a group of target genes, entire protein coding regions of the human genome, and the whole human genome has become a reality. Next Generation Sequencing (NGS) or Massively Parallel Sequencing (MPS) technologies offers a way to screen for mutations in many different genes in a cost and time efficient manner by deep coverage of the target sequences. This novel technology has now been applied to clinical diagnosis of Mendelian disorders of well characterized or undefined diseases, discovery of new disease genes, noninvasive prenatal diagnosis using maternal blood, and population based carrier testing of severe autosomal recessive disorders.

ISBN: 9789463006422

Standard No.: 10.1007/978-94-6300-642-2doiSubjects--Topical Terms:

2002405
Generation Y
--Education.

LC Class. No.: HQ799.5 / .G754 2016

Dewey Class. No.: 305.2

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520 $a This book covers topics of these applications, including potential limitations and expanded application in the future. To the fast development of a variety of Next Geners technologies in the post human genome project era, sequencing analysis of a group of target genes, entire protein coding regions of the human genome, and the whole human genome has become a reality. Next Generation Sequencing (NGS) or Massively Parallel Sequencing (MPS) technologies offers a way to screen for mutations in many different genes in a cost and time efficient manner by deep coverage of the target sequences. This novel technology has now been applied to clinical diagnosis of Mendelian disorders of well characterized or undefined diseases, discovery of new disease genes, noninvasive prenatal diagnosis using maternal blood, and population based carrier testing of severe autosomal recessive disorders.
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