Shoufang Qu

发表

Integrative analyses of maternal plasma cell-free DNA nucleosome footprint differences reveal chromosomal aneuploidy fetuses gene expression profile

Yingsong Wu, Kun Li, Zhiwei Guo, 2022, Journal of Translational Medicine.

MGB-based one-step multiplex real-time PCR method for rapid detection of HPV.

Jie Huang, Lining Zhang, Li-cheng Liu, 2012, Cancer biomarkers : section A of Disease markers.

Single cell RNA-seq reveals cellular diversity and developmental characteristics of human infant retina

Fang Chen, Xinghuai Sun, Jixing Zhong, 2019, bioRxiv.

A reference human genome dataset of the BGISEQ-500 sequencer

Hui Jiang, Wenwei Zhang, Xinming Liang, 2017, GigaScience.

Sensitive detection of trace amounts of KRAS codon 12 mutations by a fast and novel one-step technique.

Weijun Chen, Jie Huang, Shujuan Wang, 2014, Clinical biochemistry.

A Deep-Learning Pipeline for TSS Coverage Imputation From Shallow Cell-Free DNA Sequencing

Yingsong Wu, Jie Huang, Kun Li, 2021, Frontiers in Medicine.

Mutation Screening of mtDNA Combined Targeted Exon Sequencing in a Cohort With Suspected Hereditary Optic Neuropathy

Fang Chen, Jian-kang Li, Lili Li, 2020, Translational vision science & technology.

Robust Benchmark Structural Variant Calls of An Asian Using State-of-the-art Long-read Sequencing Technologies

Yang Wang, Fei Fan, Ou Wang, 2021, Genom. Proteom. Bioinform..

Robust Benchmark Structural Variant Calls of An Asian Using the State-of-Art Long Fragment Sequencing Technologies

Yang Wang, Fei Fan, Ou Wang, 2020, bioRxiv.

Haplotype-resolved Chinese male genome assembly based on high-fidelity sequencing

K. Ye, Xiaofei Yang, Shenghan Gao, 2022, Fundamental Research.

A Reference System for BRCA Mutation Detection Based on Next-Generation Sequencing in the Chinese Population.

X. Yi, K. Shao, Y. Guan, 2019, The Journal of molecular diagnostics : JMD.

Detection of chromosomal abnormalities in spontaneous miscarriage by low-coverage next-generation sequencing

Yingsong Wu, Xuexi Yang, Fen-xia Li, 2020, Molecular medicine reports.

Influence of low tumor content on tumor mutational burden estimation by whole‐exome sequencing and targeted panel sequencing

Yanyan Zhang, Miao Li, Ling Yang, 2021, Clinical and translational medicine.

A Comparison of Matrix-Assisted Laser Desorption/Ionization Time-of-Flight Mass Spectrometry and Surface Plasmon Resonance for Genotyping of High-Risk Human Papillomaviruses

Weijun Chen, Jie Huang, Li-cheng Liu, 2011, Intervirology.

An integrated Asian human SNV and indel benchmark established using multiple sequencing methods

Jie Huang, Ting Yu, Yangyi Chen, 2020, Scientific Reports.

BDdb: a comprehensive platform for exploration and utilization of birth defect multi-omics data

Xiuqing Zhang, Shoufang Qu, Fang Chen, 2020, bioRxiv.

Construction of a reference material panel for detecting KRAS/NRAS/EGFR/BRAF/MET mutations in plasma ctDNA

Jie Huang, Juanli Zhang, Jun Xu, 2020, Journal of Clinical Pathology.

Simulated confined placental mosaicism proportion (SCPMP) based on cell‐free fetal DNA fraction enrichment can reduce false‐positive results in non‐invasive prenatal testing

Yingsong Wu, Shou-fang Qu, Kun Li, 2022, Prenatal diagnosis.

The Setup and Application of Reference Material in Sequencing-Based Noninvasive Prenatal Testing

Yanyan Zhang, Hui Jiang, F. Mu, 2021, Gynecologic and Obstetric Investigation.

A novel RFLP-ARMS TaqMan PCR-based method for detecting the BRAF V600E mutation in melanoma

Weijun Chen, Jie Huang, Jinyin Zhao, 2018, Oncology letters.

An integrated Asian human SNV and indel benchmark combining multiple sequencing methods

Xinming Liang, Guangyi Fan, Jiezhong Zhang, 2019, bioRxiv.

Development of a Genomic DNA Reference Material Panel for Thalassemia Genetic Testing

Fengxiang Wei, Shou-fang Qu, Jie Huang, 2019, bioRxiv.

Comprehensive evaluation of BRCA1/2 variant interpretation ability among laboratories in China

Kui Wu, K. Shao, Lusheng Wang, 2021, Journal of Medical Genetics.

Erratum to: A reference human genome dataset of the BGISEQ-500 sequencer

Wenwei Zhang, Hui Jiang, Yuxiang Li, 2018, GigaScience.

Restriction endonuclease‐mediated real‐time digestion‐PCR for somatic mutation detection

Weijun Chen, Jing Zhao, W. Zhong, 2013, International journal of cancer.

Non-cell Corynebacterium parvum generated by nanotechnology: a promising immunomodulator with less side effects.

Lining Zhang, Chun Guo, Pin Zhang, 2007, International immunopharmacology.

Detection of low-level DNA mutation by ARMS-blocker-Tm PCR.

Weijun Chen, Jie Huang, Mengzhao Wang, 2016, Clinical biochemistry.

Nanopore Third-Generation Sequencing for Comprehensive Analysis of Hemoglobinopathy Variants.

Wanjun Zhou, Wanqing Han, Weilun Huang, 2023, Clinical chemistry.

An integrated Asian human SNV and indel benchmark established using multiple sequencing methods

Guangyi Fan, Junhua Rao, Xinming Liang, 2020, Scientific Reports.

Development and characterization of reference materials for EGFR, KRAS, NRAS, BRAF, PIK3CA, ALK, and MET genetic testing.

Yingsong Wu, Shou-fang Qu, Jie Huang, 2022, Technology and health care : official journal of the European Society for Engineering and Medicine.