Qiang Liu

Ying-ru Zheng, Jian-xin Guo, Qiang Liu, 2011, International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics.

Analysis of Cancer Mutation Signatures in Blood by a Novel Ultra-Sensitive Assay: Monitoring of Therapy or Recurrence in Non-Metastatic Breast Cancer

S. Sommer, Jinong Feng, L. Weiss, 2009, PloS one.

Elevated frequency of ATM gene missense mutations in breast cancer relative to ethnically matched controls.

W. Bennett, M. Jung, A. Dritschilo, 2002, Cancer genetics and cytogenetics.

Microarray-based DNA resequencing using 3' blocked primers.

S. Sommer, Qiang Liu, J. Sram, 2008, Analytical biochemistry.

Detection of ultrarare somatic mutation in the human TP53 gene by bidirectional pyrophosphorolysis‐activated polymerization allele‐specific amplification

S. Sommer, Jinxiu Shi, Qiang Liu, 2007, Human mutation.

Robust Dosage PCR (RD‐PCR) for Highly Accurate Dosage Analysis

S. Sommer, Qiang Liu, V. Nguyen, 2009, Current protocols in human genetics.

A large-scale validation of dosage analysis by robust dosage-polymerase chain reaction.

S. Sommer, Qiang Liu, V. Nguyen, 2007, Analytical biochemistry.

Elimination of locus-specific inter-individual variation in quantitative PCR.

S. Sommer, Jinxiu Shi, Qiang Liu, 2004, BioTechniques.

Robust dosage-PCR for detection of heterozygous chromosomal deletions.

S. Sommer, Jiesheng Chen, Qiang Liu, 2003, BioTechniques.

Development of a PCR/Ligase Detection Reaction/Nanogold-Based Universal Array Approach for the Detection of Low-Abundant DNA Point Mutations

W. Lu, Jian-xin Guo, Qiang Liu, 2011, Cell Biochemistry and Biophysics.

Toward a fluorescent single-strand conformation polymorphism technique that detects all mutations: F-DOVAM-S.

C. Mroske, Jinong Feng, Jin Yan, 2007, Analytical biochemistry.

Single‐cell immunohistochemical mutation load assay (SCIMLA) using human paraffin‐embedded tissues

L. Weiss, K. Hill, S. Sommer, 2003, Environmental and molecular mutagenesis.

Detection of heterozygous deletions and duplications in the MECP2 gene in Rett syndrome by Robust Dosage PCR (RD‐PCR)

S. Sommer, P. Maciel, Jinong Feng, 2005, Human mutation.

Reliable multiplex sequencing with rare index mis-assignment on DNB-based NGS platform

Yuan Jiang, J. Liu, R. Drmanac, 2018, bioRxiv.

Plasma ctDNA increases tissue NGS-based detection of therapeutically targetable mutations in lung cancers

Jing Zhao, Zhenhua Huang, Wenjun Zhu, 2023, BMC Cancer.

Elevated Plasma Levels of Hypermethylated RASSF1A Gene Sequences in Pregnant Women with Intrahepatic Cholestasis

Ying-ru Zheng, Xinmei Yu, Qiang Liu, 2013, Cell Biochemistry and Biophysics.

Multiplex Detection of Mutations in Clinical Isolates of Rifampin-Resistant Mycobacterium tuberculosis by Short Oligonucleotide Ligation Assay on DNA Chips

Zhi-ping Zhang, Xian-En Zhang, Jiao-yu Deng, 2004, Journal of Clinical Microbiology.

Oligonucleotide ligation assay-based DNA chip for multiplex detection of single nucleotide polymorphism.

Y. Mang, Zhi-ping Zhang, Xian-En Zhang, 2004, Biosensors & bioelectronics.

Subcycling-PCR for multiplex long-distance amplification of regions with high and low GC content: application to the inversion hotspot in the factor VIII gene.

S. Sommer, Q. Liu, Qiang Liu, 1998, BioTechniques.

Single-tube polymerase chain reaction for rapid diagnosis of the inversion hotspot of mutation in hemophilia A.

S. Sommer, Q. Liu, G. Nozari, 1998, Blood.

An assay of gene copy number and its application based on heteroduplex products.

Jing-zhong Liu, Qiang Liu, X. Jia, 2011, Experimental and molecular pathology.

Overlapping PCR for bidirectional PCR amplification of specific alleles: a rapid one-tube method for simultaneously differentiating homozygotes and heterozygotes.

E. Thorland, J. Heit, S. Sommer, 1997, Genome research.

Reliable multiplex sequencing with rare index mis-assignment on DNB-based NGS platform

Jian Wang, Xun Xu, Hui Jiang, 2018, BMC Genomics.

Pyrophosphorolysis-activated polymerization (PAP): application to allele-specific amplification.

S. Sommer, Q. Liu, Qiang Liu, 2000, BioTechniques.

A population-based case-control study of the tumor necrosis factor alpha-308 polymorphism in multiple sclerosis

B. Weinshenker, S. Sommer, D. Wingerchuk, 1997, Neurology.

"Cryptic" repeating triplets of purines and pyrimidines (cRRY(i)) are frequent and polymorphic: analysis of coding cRRY(i) in the proopiomelanocortin (POMC) and TATA-binding protein (TBP) genes.

B. Gostout, S. Sommer, Q. Liu, 1993, American journal of human genetics.

Genotypic detection of Mycobacterium tuberculosis rifampin resistance: comparison of single-strand conformation polymorphism and dideoxy fingerprinting

D. Persing, Diana J L Williams, D. Williams, 1995, Journal of clinical microbiology.