N. Qu

发表

The sequence and de novo assembly of the giant panda genome

Dawei Li, Huanming Yang, Jian Wang, 2010, Nature.

Noninvasive Prenatal Paternity Testing with a Combination of Well-Established SNP and STR Markers Using Massively Parallel Sequencing

N. Qu, Hai-xia Li, D. Peng, 2021, Genes.

Transcriptome and Network Changes in Climbers at Extreme Altitudes

Christopher D. Green, Huanming Yang, Jian Wang, 2012, PloS one.

The sequence and de novo assembly of the giant panda genome

Dawei Li, Huanming Yang, Jian Wang, 2010, Nature.

A novel mutation of the SLC25A13 gene in a Chinese patient with citrin deficiency detected by target next-generation sequencing.

X. Yi, N. Qu, Hanlin Zhou, 2014, Gene.

Noninvasive prenatal paternity testing by maternal plasma DNA sequencing in twin pregnancies

Yanyan Zhang, Xiuqing Zhang, N. Qu, 2020, Electrophoresis.

Noninvasive prenatal paternity testing using targeted massively parallel sequencing

N. Qu, Shaobin Lin, X. Ou, 2018, Transfusion.

Targeted next-generation sequencing as a comprehensive test for patients with and female carriers of DMD/BMD: a multi-population diagnostic study

X. Yi, Jun Wang, L. Cui, 2013, European Journal of Human Genetics.

Evaluation of the Genetic Variation Spectrum Related to Corneal Dystrophy in a Large Cohort

W. He, K. Shao, N. Qu, 2021, Frontiers in Cell and Developmental Biology.

Identification of Sequence Variants in Genetic Disease-Causing Genes Using Targeted Next-Generation Sequencing

Hui Jiang, Xin Yi, Qian Zhu, 2011, PloS one.

Analysis of a Chinese pedigree with Zellweger syndrome reveals a novel PEX1 mutation by next-generation sequencing.

X. Yi, N. Qu, Shuang Yang, 2013, Clinica chimica acta; international journal of clinical chemistry.

Next-generation sequencing identifies a novel compound heterozygous mutation in MYO7A in a Chinese patient with Usher Syndrome 1B.

X. Yi, N. Qu, Yu Liang, 2012, Clinica chimica acta; international journal of clinical chemistry.

Detection of truncated dystrophin lacking the C-terminal domain in a Chinese pedigree by next-generation sequencing.

X. Yi, N. Qu, P. Yu, 2012, Gene.

A novel mutation of IDS gene in a Chinese patient with mucopolysaccharidosis II by next-generation sequencing.

X. Yi, N. Qu, F. Jin, 2011, Clinica chimica acta; international journal of clinical chemistry.

The sequence and de novo assembly of the giant panda genome

Dawei Li, Huanming Yang, Jian Wang, 2010, Nature.

Detection of fetal sex chromosome aneuploidy by massively parallel sequencing of maternal plasma DNA: initial experience in a Chinese hospital

Y. Liu, H. Zhang, N. Qu, 2014, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Analysis of genetic polymorphisms and mutations at 23 autosomal STR loci in Guangdong Han population.

N. Qu, X. Ou, H. Liang, 2019, Forensic science international. Genetics.

Noninvasive prenatal paternity testing by target sequencing microhaps.

N. Qu, X. Ou, 2020, Forensic science international. Genetics.

A microhap panel for kinship analysis through massively parallel sequencing technology

N. Qu, Shaobin Lin, X. Ou, 2019, Electrophoresis.

The sequence and de novo assembly of the giant panda genome

Dawei Li, Huanming Yang, Jian Wang, 2010, Nature.