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Author Details
Full Name
Mark S Chee
Affiliation
Medical Research Council Laboratory of Molecular Biology
ORCID
Career Start Year
1989
Papers
51
H Index
38
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
33495758
Epitope-resolved profiling of the SARS-CoV-2 antibody response identifies cross-reactivity with endemic human coronaviruses.
Cell Rep Med
2021
32163288
National Cancer Institute Think-Tank Meeting Report on Proteomic Cartography and Biomarkers at the Single-Cell Level: Interrogation of Premalignant Lesions.
J Proteome Res
2020
32743570
Epitope-resolved profiling of the SARS-CoV-2 antibody response identifies cross-reactivity with an endemic human CoV.
bioRxiv
2020
24563622
Personalized ovarian cancer disease surveillance and detection of candidate therapeutic drug target in circulating tumor DNA.
Neoplasia
2014
23335997
High-resolution analysis and functional mapping of cleavage sites and substrate proteins of furin in the human proteome.
PLoS One
2013
22558217
New details of HCV NS3/4A proteinase functionality revealed by a high-throughput cleavage assay.
PLoS One
2012
22701568
A highly scalable peptide-based assay system for proteomics.
PLoS One
2012
21036922
Discovery of non-ETS gene fusions in human prostate cancer using next-generation RNA sequencing.
Genome Res
2011
22185227
Detection of low prevalence somatic mutations in solid tumors with ultra-deep targeted sequencing.
Genome Biol
2011
20964841
FusionSeq: a modular framework for finding gene fusions by analyzing paired-end RNA-sequencing data.
Genome Biol
2010
19638418
Microarray-based multicycle-enrichment of genomic subsets for targeted next-generation sequencing.
Genome Res
2009
19622793
Quantitative phenotyping via deep barcode sequencing.
Genome Res
2009
19649210
N-myc downstream regulated gene 1 (NDRG1) is fused to ERG in prostate cancer.
Neoplasia
2009
17943122
A second generation human haplotype map of over 3.1 million SNPs.
Nature
2007
17943131
Genome-wide detection and characterization of positive selection in human populations.
Nature
2007
16449502
High-throughput DNA methylation profiling using universal bead arrays.
Genome Res
2006
16847463
Highly parallel genomic assays.
Nat Rev Genet
2006
15838508
A genome-wide scalable SNP genotyping assay using microarray technology.
Nat Genet
2005
15078854
Decoding randomly ordered DNA arrays.
Genome Res
2004
15520296
A novel, high-performance random array platform for quantitative gene expression profiling.
Genome Res
2004
15782173
A highly informative SNP linkage panel for human genetic studies.
Nat Methods
2004
15509548
Quantitative gene expression profiling in formalin-fixed, paraffin-embedded tissues using universal bead arrays.
Am J Pathol
2004
15048786
Efficient strategies for the conjugation of oligonucleotides to antibodies enabling highly sensitive protein detection.
Biopolymers
2004
15123585
A versatile assay for high-throughput gene expression profiling on universal array matrices.
Genome Res
2004
15338605
Highly parallel SNP genotyping.
Cold Spring Harb Symp Quant Biol
2003
11923840
Profiling alternative splicing on fiber-optic arrays.
Nat Biotechnol
2002
12083399
BeadArray technology: enabling an accurate, cost-effective approach to high-throughput genotyping.
Biotechniques
2002
10958631
Genome-wide detection of allelic imbalance using human SNPs and high-density DNA arrays.
Genome Res
2000
10037810
A novel method for determining linkage between DNA sequences: hybridization to paired probe arrays.
Nucleic Acids Res
1999
9847078
Mutation detection by ligation to complete n-mer DNA arrays.
Genome Res
1998
9582121
Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome.
Science
1998
9191940
Genetic content and preliminary transcriptional analysis of a representative region of murine gammaherpesvirus 68.
J Gen Virol
1997
8673920
Extensive polymorphisms observed in HIV-1 clade B protease gene using high-density oligonucleotide arrays.
Nat Med
1996
9634850
Expression monitoring by hybridization to high-density oligonucleotide arrays.
Nat Biotechnol
1996
8944024
Detection of heterozygous mutations in BRCA1 using high density oligonucleotide arrays and two-colour fluorescence analysis.
Nat Genet
1996
8849452
Accessing genetic information with high-density DNA arrays.
Science
1996
7495558
Using oligonucleotide probe arrays to access genetic diversity.
Biotechniques
1995
8510532
Preparation and fluorescent sequencing of M13 clones: microtiter methods.
Methods Enzymol
1993
1319559
Human cytomegalovirus UL97 open reading frame encodes a protein that phosphorylates the antiviral nucleoside analogue ganciclovir.
Nature
1992
1666311
The DNA sequence of the human cytomegalovirus genome.
DNA Seq
1991
1753940
Subfamilies of serine tRNA genes in the bovine genome.
Mol Gen Genet
1991
1762928
A simple method for sequencing the complementary strand of ssDNA from M13 clones.
Nucleic Acids Res
1991
1648828
The HCMV genome project: what has been learned and what can be expected in the future.
Transplant Proc
1991
1891372
Single stranded rescue from phagemids in microtitre plates.
Nucleic Acids Res
1991
2062645
Enzymatic multiplex DNA sequencing.
Nucleic Acids Res
1991
2183417
Herpesviruses: a study of parts.
Trends Genet
1990
2152817
Human herpesvirus 6 is closely related to human cytomegalovirus.
J Virol
1990
2158627
Human cytomegalovirus encodes three G protein-coupled receptor homologues.
Nature
1990
2161319
Analysis of the protein-coding content of the sequence of human cytomegalovirus strain AD169.
Curr Top Microbiol Immunol
1990
2536837
Identification of the major capsid protein gene of human cytomegalovirus.
J Virol
1989
1 - 50 of 51
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