(Q45049473)

8 December 2017

title

A method for noninvasive detection of fetal large deletions/duplications by low coverage massively parallel sequencing (English)

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8 December 2017

Jun Wang

21

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Tze Kin Lau

object named as

Tze Kin Lau

2

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author name string

Shengpei Chen

1

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8 December 2017

Chunlei Zhang

3

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8 December 2017

Chenming Xu

4

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8 December 2017

Zhengfeng Xu

5

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8 December 2017

Ping Hu

6

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8 December 2017

Jian Xu

7

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8 December 2017

Hefeng Huang

8

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8 December 2017

Ling Pan

9

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8 December 2017

Fuman Jiang

10

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8 December 2017

Fang Chen

11

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8 December 2017

Xiaoyu Pan

12

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8 December 2017

Weiwei Xie

13

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8 December 2017

Ping Liu

14

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8 December 2017

Xuchao Li

15

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8 December 2017

Lei Zhang

16

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8 December 2017

Songgang Li

17

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8 December 2017

Yingrui Li

18

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8 December 2017

Xun Xu

19

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8 December 2017

Wei Wang

20

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8 December 2017

Hui Jiang

22

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8 December 2017

Xiuqing Zhang

23

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8 December 2017

publication date

1 June 2013

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8 December 2017

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8 December 2017

volume

33

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8 December 2017

issue

6

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8 December 2017

page(s)

584-590

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Copy number variation: new insights in genome diversity

8 December 2017

cites work

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Copy-number variation and association studies of human disease

21 January 2018

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Copy number variants and genetic traits: closer to the resolution of phenotypic to genotypic variability

21 January 2018

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'Puppet' children. A report on three cases (1965).

21 January 2018

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From prenatal genomic diagnosis to fetal personalized medicine: progress and challenges

21 January 2018

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Invasive procedures for prenatal diagnosis: any future left?

21 January 2018

1 reference

Noninvasive prenatal diagnosis of common fetal chromosomal aneuploidies by maternal plasma DNA sequencing.

21 January 2018

1 reference

DNA sequencing of maternal plasma reliably identifies trisomy 18 and trisomy 13 as well as Down syndrome: an international collaborative study

21 January 2018

1 reference

Non-Invasive Chromosomal Evaluation (NICE) Study: results of a multicenter prospective cohort study for detection of fetal trisomy 21 and trisomy 18.

21 January 2018

1 reference

Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencing

21 January 2018

1 reference

Noninvasive prenatal diagnosis of a fetal microdeletion syndrome

21 January 2018

1 reference

Detection of microdeletion 22q11.2 in a fetus by next-generation sequencing of maternal plasma

21 January 2018

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Noninvasive detection of fetal subchromosome abnormalities via deep sequencing of maternal plasma

21 January 2018

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Sensitivity of noninvasive prenatal detection of fetal aneuploidy from maternal plasma using shotgun sequencing is limited only by counting statistics

21 January 2018

1 reference

Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma

21 January 2018

1 reference

Maternal plasma DNA analysis with massively parallel sequencing by ligation for noninvasive prenatal diagnosis of trisomy 21.

21 January 2018

1 reference

High-resolution mapping of copy-number alterations with massively parallel sequencing

21 January 2018

1 reference

SOAP2: an improved ultrafast tool for short read alignment

21 January 2018

1 reference

Analyzing and minimizing PCR amplification bias in Illumina sequencing libraries

21 January 2018

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Microdeletion and microduplication syndromes.

21 January 2018

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Presence of fetal DNA in maternal plasma and serum

21 January 2018

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21 January 2018

Identifiers

DOI

10.1002/PD.4110

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8 December 2017

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