D. Ganesamoorthy

发表

Application of a new molecular technique for the genetic evaluation of products of conception

F. Vialard, G. Simoni, A. Aboura, 2013, Prenatal diagnosis.

Analysis of polyclonal vector integration sites using Nanopore sequencing as a scalable, cost-effective platform

L. Coin, D. Ganesamoorthy, S. H. Nguyen, 2019 .

Phase I Trial of Inducible Caspase 9 T Cells in Adult Stem Cell Transplant Demonstrates Massive Clonotypic Proliferative Potential and Long-term Persistence of Transgenic T Cells

L. Coin, M. Brown, T. Gargett, 2019, Clinical Cancer Research.

Extending the scope of diagnostic chromosome analysis: Detection of single gene defects using high‐resolution SNP microarrays

Z. Stark, P. James, D. O’Rielly, 2011, Human mutation.

High-throughput multiplexed tandem repeat genotyping using targeted long-read sequencing

Minh Duc Cao, L. Coin, V. Murigneux, 2020 .

High-throughput multiplexed tandem repeat genotyping using targeted long-read sequencing

Minh Duc Cao, L. Coin, V. Murigneux, 2019, bioRxiv.

sCNAphase: using haplotype resolved read depth to genotype somatic copy number alterations from low cellularity aneuploid tumors

L. Coin, Alan J. Robertson, D. Ganesamoorthy, 2016, bioRxiv.

Real-time identification of pathogens and antibiotic resistance using Oxford Nanopore MinION sequencing

Minh Duc Cao, L. Coin, M. Cooper, 2015 .

High‐resolution microarray in the assessment of fetal anomalies detected by ultrasound

G. McGillivray, D. Ganesamoorthy, R. Palma-Dias, 2014, The Australian & New Zealand journal of obstetrics & gynaecology.

npInv: accurate detection and genotyping of inversions using long read sub-alignment

Minh Duc Cao, C. Hoggart, L. Coin, 2018, BMC Bioinformatics.

GtTR: Bayesian estimation of absolute tandem repeat copy number using sequence capture and high throughput sequencing

Minh Duc Cao, L. Coin, D. Ganesamoorthy, 2018, bioRxiv.

Streaming algorithms for identification of pathogens and antibiotic resistance potential from real-time MinIONTM sequencing

Minh Duc Cao, Huihui Zhang, Matthew A Cooper, 2015, bioRxiv.

Further molecular and clinical delineation of co-locating 17p13.3 microdeletions and microduplications that show distinctive phenotypes

B. V. van Bon, R. Pfundt, B. D. de Vries, 2010, Journal of Medical Genetics.

npInv: accurate detection and genotyping of inversions mediated by non-allelic homologous recombination using long read sub-alignment

Minh Duc Cao, Clive J. Hoggart, Devika Ganesamoorthy, 2017, bioRxiv.

A Genotype-First Approach for the Molecular and Clinical Characterization of Uncommon De Novo Microdeletion of 20q13.33

J. Rosenfeld, B. Torchia, L. Shaffer, 2010, PloS one.

Detection of cryptic pathogenic copy number variations and constitutional loss of heterozygosity using high resolution SNP microarray analysis in 117 patients referred for cytogenetic analysis and impact on clinical practice

I. Scheffer, K. Choy, N. Pachter, 2008, Journal of Medical Genetics.

Phenotypic variability of distal 22q11.2 copy number abnormalities

J. Crolla, A. Collins, Z. Stark, 2011, American journal of medical genetics. Part A.

Meeting the challenge of interpreting high‐resolution single nucleotide polymorphism array data in prenatal diagnosis: does increased diagnostic power outweigh the dilemma of rare variants?

M. Pertile, G. McGillivray, D. Ganesamoorthy, 2013, BJOG : an international journal of obstetrics and gynaecology.

Real-time strain typing and analysis of antibiotic resistance potential using Nanopore MinION sequencing

Minh Duc Cao, L. Coin, M. Cooper, 2015 .

Whole genome deep sequencing analysis of cell-free DNA in samples with low tumour content

Minh Duc Cao, Michael B. Hall, L. Coin, 2022, BMC Cancer.

phenotypes microduplications that show distinctive co-locating 17 p 13 . 3 microdeletions and Further molecular and clinical delineation of

R. Pfundt, C. Martin, A. Wallin, 2022 .

Methylation of novel markers of fragile X alleles is inversely correlated with FMRP expression and FMR1 activation ratio.

D. Loesch, F. Tassone, R. Hagerman, 2010, Human molecular genetics.

Molecular and clinical characterization of 25 individuals with exonic deletions of NRXN1 and comprehensive review of the literature

S. Antonarakis, S. Gimelli, F. Béna, 2013, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Octapeptin C4 and polymyxin resistance occur via distinct pathways in an epidemic XDR Klebsiella pneumoniae ST258 isolate

Minh Duc Cao, L. Coin, M. Cooper, 2018, The Journal of antimicrobial chemotherapy.

Octapeptin C4 Induces Less Resistance and Novel Mutations in an Epidemic Carbapenemase-producing Klebsiella pneumoniae ST258 Clinical Isolate Compared to Polymyxins

Minh Duc Cao, L. Coin, M. Cooper, 2018, bioRxiv.

Development of a multiplex ligation-dependent probe amplification assay for diagnosis and estimation of the frequency of spinocerebellar ataxia type 15.

E. Storey, M. Delatycki, J. Schoumans, 2009, Clinical chemistry.

Pathogenic aberrations revealed exclusively by single nucleotide polymorphism (SNP) genotyping data in 5000 samples tested by molecular karyotyping

Z. Stark, M. Pertile, D. Francis, 2011, Journal of Medical Genetics.

Investigating and Correcting Plasma DNA Sequencing Coverage Bias to Enhance Aneuploidy Discovery

Terence P. Speed, Melanie Bahlo, Devika Ganesamoorthy, 2014, PloS one.

Scaffolding and completing genome assemblies in real-time with nanopore sequencing

Minh Duc Cao, Son Hoang Nguyen, Matthew A Cooper, 2016, Nature Communications.

Profiling copy number alterations in cell-free tumour DNA using a single-reference

Peter T. Simpson, Qinying Xu, Sunil R. Lakhani, 2018, bioRxiv.

Multifactorial chromosomal variants regulate polymyxin resistance in extensively drug-resistant Klebsiella pneumoniae

Minh Duc Cao, L. Coin, M. Cooper, 2017, bioRxiv.

Use of copy number deletion polymorphisms to assess DNA chimerism.

N. Thorne, D. Power, M. Bahlo, 2014, Clinical chemistry.

Simulating the dynamics of targeted capture sequencing with CapSim

Lachlan James M. Coin, Minh Duc Cao, Chenxi Zhou, 2017, bioRxiv.

Nanopore sequencing as a scalable, cost-effective platform for analyzing polyclonal vector integration sites following clinical T cell therapy

L. Coin, D. Ganesamoorthy, S. H. Nguyen, 2020, Journal for immunotherapy of cancer.

GtTR: Bayesian estimation of absolute tandem repeat copy number using sequence capture and high throughput sequencing

Lachlan James M. Coin, Minh Duc Cao, Tania P. S. Duarte, 2018, BMC Bioinformatics.

npInv: accurate detection and genotyping of inversions using long read sub-alignment

Lachlan James M. Coin, Minh Duc Cao, Tania P. S. Duarte, 2018, BMC Bioinformatics.

Complete Genome Sequence of Klebsiella quasipneumoniae subsp. similipneumoniae Strain ATCC 700603

Minh Duc Cao, Matthew A. Cooper, Devika Ganesamoorthy, 2016, Genome Announcements.

Host gene expression signatures to identify infection type and organ dysfunction in children evaluated for sepsis: a multicentre cohort study.

M. Kaforou, S. Bialasiewicz, D. Ganesamoorthy, 2024, The Lancet. Child & adolescent health.