(Q51166178)

31 March 2018

title

A short-read multiplex sequencing method for reliable, cost-effective and high-throughput genotyping in large-scale studies. (English)

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31 March 2018

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23

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31 March 2018

Jun Wang

object named as

Jun Wang

25

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Karsten Kristiansen

24

object named as

Karsten Kristiansen

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31 March 2018

Hongzhi Cao

1

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31 March 2018

Yu Wang

2

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31 March 2018

Wei Zhang

3

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31 March 2018

Xianghua Chai

4

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31 March 2018

Xiandong Zhang

5

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31 March 2018

Shiping Chen

6

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31 March 2018

Fan Yang

7

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31 March 2018

Caifen Zhang

8

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31 March 2018

Yulai Guo

9

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31 March 2018

Ying Liu

10

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31 March 2018

Zhoubiao Tang

11

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31 March 2018

Caifen Chen

12

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31 March 2018

Yaxin Xue

13

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31 March 2018

Hefu Zhen

14

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31 March 2018

Yinyin Xu

15

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31 March 2018

Bin Rao

16

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31 March 2018

Tao Liu

17

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31 March 2018

Meiru Zhao

18

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31 March 2018

Wenwei Zhang

19

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31 March 2018

Yingrui Li

20

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31 March 2018

Xiuqing Zhang

21

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31 March 2018

Laurent C A M Tellier

22

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31 March 2018

Jian Li

26

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31 March 2018

publication date

7 October 2013

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31 March 2018

published in

Human Mutation

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31 March 2018

volume

34

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31 March 2018

issue

12

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31 March 2018

page(s)

1715-1720

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31 March 2018

Exome sequencing as a tool for Mendelian disease gene discovery

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Carrier testing for severe childhood recessive diseases by next-generation sequencing

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High-resolution, high-throughput HLA genotyping by next-generation sequencing

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Rapid, scalable and highly automated HLA genotyping using next-generation sequencing: a transition from research to diagnostics

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21 January 2018

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21 January 2018

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21 January 2018

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Fast and accurate short read alignment with Burrows-Wheeler transform

21 January 2018

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Mapping short DNA sequencing reads and calling variants using mapping quality scores

21 January 2018

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Sequencing technologies - the next generation

21 January 2018

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Rapid and specific genotyping system for hepatitis B virus corresponding to six major genotypes by PCR using type-specific primers

21 January 2018

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Genetic testing in the long QT syndrome: development and validation of an efficient approach to genotyping in clinical practice.

21 January 2018

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Template-switching during DNA synthesis byThermus aquaticusDNA polymerase I

21 January 2018

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Next-generation sequencing: from basic research to diagnostics

21 January 2018

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High-throughput, high-fidelity HLA genotyping with deep sequencing

21 January 2018

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Comprehensive method for the typing of HLA-A, B, and C alleles by direct sequencing of PCR products obtained from genomic DNA

21 January 2018

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inferred from DOI database lookup

7 January 2021

based on heuristic

Carrier screening for alpha- and beta-thalassemia in pregnancy: the results of an 11-year prospective program in Guangzhou Maternal and Neonatal hospital

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22439

inferred from DOI database lookup

7 January 2021

based on heuristic

Large-scale oligonucleotide typing for HLA-DRB1/3/4 and HLA-DQB1 is highly accurate, specific, and reliable

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22439

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1002/HUMU.22439

1 reference

31 March 2018

1 reference

31 March 2018