Author details

Full Name

Ming Xiao

Affiliation

Drexel University

ORCID

Career Start Year

1998

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37372458	Single-Molecule Telomere Assay via Optical Mapping (SMTA-OM) Can Potentially Define the ALT Positivity of Cancer.	Genes (Basel)	2023
35444207	Multiplex structural variant detection by whole-genome mapping and nanopore sequencing.	Sci Rep	2022
31056507	Analysis of Subtelomeric REXTAL Assemblies Using QUAST.	IEEE/ACM Trans Comput Biol Bioinform	2021
34534648	Characterization of full-length LINE-1 insertions in 154 genomes.	Genomics	2021
34232611	Multicolor Whole-Genome Mapping in Nanochannels for Genetic Analysis.	Anal Chem	2021
33310082	Single-molecule telomere length characterization by optical mapping in nano-channel array: Perspective and review on telomere length measurement.	Environ Toxicol Pharmacol	2021
33231685	Customized optical mapping by CRISPR-Cas9 mediated DNA labeling with multiple sgRNAs.	Nucleic Acids Res	2021
32669102	Single-molecule analysis of subtelomeres and telomeres in Alternative Lengthening of Telomeres (ALT) cells.	BMC Genomics	2020
31754017	The Driver of Extreme Human-Specific Olduvai Repeat Expansion Remains Highly Active in the Human Genome.	Genetics	2020
31986135	Comprehensive Analysis of Human Subtelomeres by Whole Genome Mapping.	PLoS Genet	2020
33127893	Towards a reference genome that captures global genetic diversity.	Nat Commun	2020
30833565	Genome maps across 26 human populations reveal population-specific patterns of structural variation.	Nat Commun	2019
31640553	Genome rearrangements induce biofilm formation in Escherichia coli C - an old model organism with a new application in biofilm research.	BMC Genomics	2019
31636335	A micropatterned substrate for on-surface enzymatic labelling of linearized long DNA molecules.	Sci Rep	2019
31416423	Evaluating the quality of the 1000 genomes project data.	BMC Genomics	2019
31481461	The 22q11 low copy repeats are characterized by unprecedented size and structural variability.	Genome Res	2019
32016171	REXTAL: Regional Extension of Assemblies Using Linked-Reads.	Bioinform Res Appl (2018)	2018
29195502	OMSV enables accurate and comprehensive identification of large structural variations from nanochannel-based single-molecule optical maps.	Genome Biol	2017
28172448	OMBlast: alignment tool for optical mapping using a seed-and-extend approach.	Bioinformatics	2017
28180280	High-throughput single-molecule mapping links subtelomeric variants and long-range haplotypes with specific telomeres.	Nucleic Acids Res	2017
29025896	High-throughput single-molecule telomere characterization.	Genome Res	2017
26481349	CRISPR-CAS9 D10A nickase target-specific fluorescent labeling of double strand DNA for whole genome mapping and structural variation analysis.	Nucleic Acids Res	2016
26510793	Genome-Wide Structural Variation Detection by Genome Mapping on Nanochannel Arrays.	Genetics	2016
23405223	Rapid genome mapping in nanochannel arrays for highly complete and accurate de novo sequence assembly of the complex Aegilops tauschii genome.	PLoS One	2013
22698062	Multicolor super-resolution DNA imaging for genetic analysis.	Nano Lett	2012
22797562	Genome mapping on nanochannel arrays for structural variation analysis and sequence assembly.	Nat Biotechnol	2012
21423606	Transition between two regimes describing internal fluctuation of DNA in a nanochannel.	PLoS One	2011
20699272	Single molecule linear analysis of DNA in nano-channel labeled with sequence specific fluorescent probes.	Nucleic Acids Res	2010
19198595	Direct determination of haplotypes from single DNA molecules.	Nat Methods	2009
17175538	Rapid DNA mapping by fluorescent single molecule detection.	Nucleic Acids Res	2007
17943131	Genome-wide detection and characterization of positive selection in human populations.	Nature	2007
17943122	A second generation human haplotype map of over 3.1 million SNPs.	Nature	2007
17443670	Determination of haplotypes from single DNA molecules: a method for single-molecule barcoding.	Hum Mutat	2007
17404718	Identification of NR1I2 genetic variation using resequencing.	Eur J Clin Pharmacol	2007
16288910	In vivo expression of a conditional TGF-beta1 transgene: no evidence for TGF-beta1 transgene expression in SM22alpha-tTA transgenic mice.	J Mol Cell Cardiol	2006
16971459	A simple DNA stretching method for fluorescence imaging of single DNA molecules.	Nucleic Acids Res	2006
16100403	Kinetic fluorescence-quenching detection assay for allele frequency estimation.	Methods Mol Biol	2005
16239245	Polymorphism discovery in 51 chemotherapy pathway genes.	Hum Mol Genet	2005
16224071	Regulated transgene expression in vascular smooth muscle.	Circ Res	2005
15108275	Single-molecule analysis for molecular haplotyping.	Hum Mutat	2004
15310656	Role of excess inorganic pyrophosphate in primer-extension genotyping assays.	Genome Res	2004
15475243	Pharmacogenomic assessment of carboxylesterases 1 and 2.	Genomics	2004
12545559	Kinetic FP-TDI assay for SNP allele frequency determination.	Biotechniques	2003
15338604	SNP genotyping and molecular haplotyping of DNA pools.	Cold Spring Harb Symp Quant Biol	2003
14517965	Identification of a frequent variant in ALG6, the cause of Congenital Disorder of Glycosylation-Ic.	Hum Mutat	2003
12679807	An actin-dependent conformational change in myosin.	Nat Struct Biol	2003
12727909	DNA analysis by fluorescence quenching detection.	Genome Res	2003
11972024	Holding two heads together: stability of the myosin II rod measured by resonance energy transfer between the heads.	Proc Natl Acad Sci U S A	2002
11459485	Quantum yields of luminescent lanthanide chelates and far-red dyes measured by resonance energy transfer.	J Am Chem Soc	2001
10452801	A comparison between the sulfhydryl reductants tris(2-carboxyethyl)phosphine and dithiothreitol for use in protein biochemistry.	Anal Biochem	1999

1 - 50 of 51

Ryan Tewhey

University of Maine

Career Start Year 2007

Number of shared co-authors 17

Xiaobei Zhao

University of Tennessee Health Science Center

Career Start Year 2007

Number of shared co-authors 0

Stephan Ossowski

Institute of Medical Genetics and Applied Genomics, University of Tubingen

Career Start Year 2006

Number of shared co-authors 2

Kun Zhang

China Pharmaceutical University

Career Start Year 2005

Number of shared co-authors 2

Robert Sebra

Icahn School of Medicine at Mount Sinai

Career Start Year 2004

Number of shared co-authors 12

Max K??ller

KTH Royal Institute of Technology

Career Start Year 2003

Number of shared co-authors 0

Ali Bashir

Google Accelerated Science Team, Google Inc

Career Start Year 2003

Number of shared co-authors 10

John Aach

Harvard Medical School

Career Start Year 2000

Number of shared co-authors 1

Eileen T Dimalanta

New England Biolabs Inc.

Career Start Year 1999

Number of shared co-authors 1

Chao Xing

University of Texas Southwestern Medical Center

Career Start Year 1999

Number of shared co-authors 5

Sarah J Wheelan

National Human Genome Research Institute, National Institutes of Health

Career Start Year 1998

Number of shared co-authors 11

Jay Shendure

University of Washington

Career Start Year 1996

Number of shared co-authors 20

Kenneth B Beckman

University of Minnesota Genomics Center (UMNGC)

Career Start Year 1996

Number of shared co-authors 2

Marco A Azaro

The State University of New Jersey

Career Start Year 1995

Number of shared co-authors 0

Jared C Roach

Institute for Systems Biology

Career Start Year 1995

Number of shared co-authors 3

Stephen R Quake

Stanford University

Career Start Year 1994

Number of shared co-authors 2

Ivo Gut

Spain Universitat de Barcelona (UB)

Career Start Year 1991

Number of shared co-authors 22

Joakim Lundeberg

KTH Royal Institute of Technology

Career Start Year 1990

Number of shared co-authors 2

Anthony J Brookes

University of Leicester

Career Start Year 1989

Number of shared co-authors 24

Mats Nilsson

Stockholm University

Career Start Year 1988

Number of shared co-authors 3

Ian Dunham

European Bioinformatics Institute (EMBL-EBI)

Career Start Year 1987

Number of shared co-authors 53

Jiannis Ragoussis

McGill University

Career Start Year 1986

Number of shared co-authors 20

John D McPherson

Ontario Institute for Cancer Research

Career Start Year 1986

Number of shared co-authors 48

Andreas Gnirke

The Center for Genome Architecture, Baylor College of Medicine

Career Start Year 1986

Number of shared co-authors 18

David C Schwartz

University of Wisconsin-Madison

Career Start Year 1983

Number of shared co-authors 13

Peter K Rogan

CytoGnomix Inc.

Career Start Year 1981

Number of shared co-authors 1

Richard M Myers

HudsonAlpha Institute for Biotechnology

Career Start Year 1980

Number of shared co-authors 54

George M Church

Harvard Medical School

Career Start Year 1977

Number of shared co-authors 13

Deborah A Nickerson

University of Washington

Career Start Year 1976

Number of shared co-authors 43

Ronald W Davis

Stanford University

Career Start Year 1968

Number of shared co-authors 36

row(s) 1 - 30 of 30

Pui-Yan Kwok

Cardiovascular Research Institute, University of California San Francisco

Co-authored papers 29

Alex R Hastie

Co-authored papers 5

Dongmei Cai

Fudan University

Co-authored papers 5

Kevin Y Yip

Co-authored papers 4

Howard L McLeod

Center for Precision Medicine and Functional Genomics, Utah Tech University

Co-authored papers 3

Yangfan Liu

Co-authored papers 2

IkeOluwapo O Ajayi

University of Ibadan

Co-authored papers 2

Michael Feolo

University of Massachusetts Medical School

Co-authored papers 2

Marcos Delgado

Co-authored papers 2

Ruth Jamieson

Newcastle University

Co-authored papers 2

John W Belmont

Illumina Inc.

Co-authored papers 2

Alexandre Montpetit

McGill University and Genome Quebec Innovation Centre

Co-authored papers 2

Chris Clee

Co-authored papers 2

Mark F Leppert

University of Utah

Co-authored papers 2

Panos Deloukas

William Harvey Research Institute, Queen Mary University of London

Co-authored papers 2

Fanny Chagnon

McGill University

Co-authored papers 2

Hongbin Zhao

First Hospital of Xingtai

Co-authored papers 2

E Clayton

Harvard Medical School, Vanderbilt University, Yale University Yale Law School

Co-authored papers 2

Jeffrey Barrett

Wellcome Trust Sanger Institute

Co-authored papers 2

Li Jin

Fudan University

Co-authored papers 2

Thomas D Willis

Adaptive Biotechnologies

Co-authored papers 2

Suzanne M Leal

Center for Statistical Genetics, Columbia University Medical Center

Co-authored papers 2

David A Hinds

23andMe Inc.

Co-authored papers 2

Ludmila Pawlikowska

Center for Cerebrovascular Research

Co-authored papers 2

Albert V Smith

University of Michigan School of Public Health ann arbor

Co-authored papers 2

Jun Yu

Beijing Institute of Genomics, Chinese Academy of Sciences

Co-authored papers 2

Jessica Roy

Co-authored papers 2

Jian-Bing Fan

Nanfang Hospital and Basic Medical College, Southern Medical University

Co-authored papers 2

Jean-Fran??ois Olivier

McGill University Health Center

Co-authored papers 2

Robert W Plumb

Co-authored papers 2

1 - 30

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