R. K. Cheetham

发表

Accurate Whole Human Genome Sequencing using Reversible Terminator Chemistry

Nancy F. Hansen, Lisa J. Murray, Phillip J. Black, 2008, Nature.

Mapping copy number variation by population scale genome sequencing

Kenny Q. Ye, G. T. Marth, Hugo Y. K. Lam, 2010, Nature.

A comprehensive catalogue of somatic mutations from a human cancer genome

Tom Royce, D. Bentley, L. Chin, 2010, Nature.

Genomic Hallmarks and Structural Variation in Metastatic Prostate Cancer

Joshua M. Stuart, Donavan T. Cheng, Luke A. Gilbert, 2018, Cell.

Genomic Diversity among Drug Sensitive and Multidrug Resistant Isolates of Mycobacterium tuberculosis with Identical DNA Fingerprints

Lisa J. Murray, G. Smith, Helen Bignell, 2009, PloS one.

PhyloSift: phylogenetic analysis of genomes and metagenomes

Henry C. M. Leung, Brian C. Thomas, Ocn, 2014, PeerJ.

Consortium, G.P A map of human genome variation from population-scale sequencing. Nature 467, 1061-1073

Ken Chen, Joshua M. Korn, Afidalina Tumian, 2010 .

Genome Sequencing and Analysis of the Tasmanian Devil and Its Transmissible Cancer

Carolyn Tregidgo, Albert J. Vilella, Peter J. Campbell, 2012, Cell.

TP53 mutations, tetraploidy and homologous recombination repair defects in early stage high-grade serous ovarian cancer

D. Bentley, R. K. Cheetham, S. Humphray, 2015, Nucleic acids research.

BIOINFORMATICS CNAseg—a novel framework for identiﬁcation of copy number changes in cancer from second-generation sequencing data

Tom Royce, S. Tavaré, D. Evers, 2010 .

Strelka: accurate somatic small-variant calling from sequenced tumor-normal sample pairs

Wendy S. W. Wong, Christopher T. Saunders, Sajani Swamy, 2012, Bioinform..

TP 53 mutations , tetraploidy and homologous recombination repair defects in early stage high-grade serous ovarian cancer

Julie, D. Bentley, R. K. Cheetham, 2015 .

APOBEC3B upregulation and genomic mutation patterns in serous ovarian carcinoma.

Jason B. Nikas, D. Bentley, R. K. Cheetham, 2013, Cancer research.

Whole-genome sequencing provides new insights into the clonal architecture of Barrett’s esophagus and esophageal adenocarcinoma

S. Tavaré, D. Bentley, R. K. Cheetham, 2015, Nature Genetics.

CNAseg - a novel framework for identification of copy number changes in cancer from second-generation sequencing data

Simon Tavaré, Anthony J. Cox, Dirk J. Evers, 2010, Bioinform..

Genomic Hallmarks and Structural Variation in Metastatic Prostate Cancer

Joshua M. Stuart, Donavan T. Cheng, Luke A. Gilbert, 2018, Cell.

Somatic genetic alterations in synchronous and metachronous low‐grade serous tumours and high‐grade carcinomas of the adnexa

Donavan T. Cheng, R. K. Cheetham, B. Weigelt, 2019, Histopathology.

Erratum: Genomic Hallmarks and Structural Variation in Metastatic Prostate Cancer (Cell (2018) 174(3) (758–769.e9), (S0092867418308420) (10.1016/j.cell.2018.06.039))

Joshua M. Stuart, Donavan T. Cheng, Luke A. Gilbert, 2018 .

Mapping copy number variation by population scale genome sequencing

Joshua M. Korn, Kenny Q. Ye, G. T. Marth, 2010, Nature.

APOBEC3B upregulation and genomic mutation patterns in serous ovarian carcinoma.

Jason B. Nikas, D. Bentley, R. K. Cheetham, 2013, Cancer Research.