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NextGenerspedagogical considerations /
~
Griffith, Bryant.
NextGenerspedagogical considerations /
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
NextGenersby Bryant Griffith.
其他題名:
pedagogical considerations /
作者:
Griffith, Bryant.
出版者:
Rotterdam :SensePublishers :2016.
面頁冊數:
xi, 144 p. :ill., digital ;24 cm.
Contained By:
Springer eBooks
標題:
Generation YEducation.
電子資源:
http://dx.doi.org/10.1007/978-94-6300-642-2
ISBN:
9789463006422$q(electronic bk.)
NextGenerspedagogical considerations /
Griffith, Bryant.
NextGeners
pedagogical considerations /[electronic resource] :by Bryant Griffith. - Rotterdam :SensePublishers :2016. - xi, 144 p. :ill., digital ;24 cm.
This book covers topics of these applications, including potential limitations and expanded application in the future. To the fast development of a variety of Next Geners technologies in the post human genome project era, sequencing analysis of a group of target genes, entire protein coding regions of the human genome, and the whole human genome has become a reality. Next Generation Sequencing (NGS) or Massively Parallel Sequencing (MPS) technologies offers a way to screen for mutations in many different genes in a cost and time efficient manner by deep coverage of the target sequences. This novel technology has now been applied to clinical diagnosis of Mendelian disorders of well characterized or undefined diseases, discovery of new disease genes, noninvasive prenatal diagnosis using maternal blood, and population based carrier testing of severe autosomal recessive disorders.
ISBN: 9789463006422$q(electronic bk.)
Standard No.: 10.1007/978-94-6300-642-2doiSubjects--Topical Terms:
618318
Generation Y
--Education.
LC Class. No.: HQ799.5 / .G754 2016
Dewey Class. No.: 305.2
NextGenerspedagogical considerations /
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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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