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Davis J. McCarthy

The University of Melbourne · AU
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Area of research
Molecular Biology · Cancer Research
Research interest
Research interests include Single-cell and spatial transcriptomics, Cancer Genomics and Diagnostics, Cell Image Analysis Techniques, and RNA Research and Splicing.
h-index
36
citations
65,311
works
167
NIH funding
primary concept
email

Recent publications

Demuxafy: improvement in droplet assignment by integrating multiple single-cell demultiplexing and doublet detection methods
Genome biology 2024cited by 65position: middledoi
Optimizing expression quantitative trait locus mapping workflows for single-cell studies
Genome biology 2021cited by 75position: middledoi
Optimising expression quantitative trait locus mapping workflows for single-cell studies
bioRxiv (Cold Spring Harbor Laboratory) 2021cited by 6position: middledoi
Eleven grand challenges in single-cell data science
Genome biology 2020cited by 1,402position: middledoi
Benchmarking single-cell RNA-sequencing protocols for cell atlas projects
Nature Biotechnology 2020cited by 527position: middledoi
Single-cell RNA-sequencing of differentiating iPS cells reveals dynamic genetic effects on gene expression
Nature Communications 2020cited by 363position: middledoi
Properties of structural variants and short tandem repeats associated with gene expression and complex traits
Nature Communications 2020cited by 136position: middledoi
Cardelino: computational integration of somatic clonal substructure and single-cell transcriptomes
Nature Methods 2020cited by 82position: firstdoi
Discovery and quality analysis of a comprehensive set of structural variants and short tandem repeats
Nature Communications 2020cited by 36position: middledoi
Publisher Correction: Single-cell RNA-sequencing of differentiating iPS cells reveals dynamic genetic effects on gene expression
Nature Communications 2020cited by 14position: middledoi
Combined single-cell profiling of expression and DNA methylation reveals splicing regulation and heterogeneity
Genome biology 2019cited by 73position: middledoi
Single-cell RNA-sequencing of differentiating iPS cells reveals dynamic genetic effects on gene expression
bioRxiv (Cold Spring Harbor Laboratory) 2019cited by 62position: middledoi
12 Grand Challenges in Single-Cell Data Science
2019cited by 7position: middledoi
Vireo: Bayesian demultiplexing of pooled single-cell RNA-seq data without genotype reference
bioRxiv (Cold Spring Harbor Laboratory) 2019cited by 6position: middledoi
12 Grand challenges in single-cell data science
2019cited by 5position: middledoi
12 Grand challenges in single-cell data science
2019cited by 2position: middledoi
12 Grand Challenges in Single-Cell Data Science
2019cited by 1position: middledoi
Visualization of Biomedical Data
Annual Review of Biomedical Data Science 2018cited by 91position: middledoi
Cardelino: Integrating whole exomes and single-cell transcriptomes to reveal phenotypic impact of somatic variants
bioRxiv (Cold Spring Harbor Laboratory) 2018cited by 15position: firstdoi
Visualization of Biomedical Data
2018cited by 9position: middledoi
Common genetic variation drives molecular heterogeneity in human iPSCs
Nature 2017cited by 635position: middledoi
f-scLVM: scalable and versatile factor analysis for single-cell RNA-seq
Genome biology 2017cited by 139position: middledoi
NOX1 loss-of-function genetic variants in patients with inflammatory bowel disease
Mucosal Immunology 2017cited by 90position: middledoi
Sequence data and association statistics from 12,940 type 2 diabetes cases and controls
Scientific Data 2017cited by 43position: middledoi
Scater: pre-processing, quality control, normalization and visualization of single-cell RNA-seq data in R
Bioinformatics 2016cited by 2,033position: firstdoi
A step-by-step workflow for low-level analysis of single-cell RNA-seq data with Bioconductor
F1000Research 2016cited by 1,810position: middledoi
The genetic architecture of type 2 diabetes
Nature 2016cited by 1,107position: middledoi
A step-by-step workflow for low-level analysis of single-cell RNA-seq data
F1000Research 2016cited by 821position: middledoi
Factors influencing success of clinical genome sequencing across a broad spectrum of disorders
Nature Genetics 2015cited by 386position: middledoi
Count-based differential expression analysis of RNA sequencing data using R and Bioconductor
Nature Protocols 2013cited by 1,226position: middledoi

Grants

No grants ingested yet.

Frequent collaborators

Oliver Stegle · Institut thématique Génétique, génomique et bioinformatique8 papers (2017–2020)Marc Jan Bonder · European Bioinformatics Institute8 papers (2018–2021)John C. Marioni · European Bioinformatics Institute4 papers (2016–2019)Daniel D. Seaton · University of Edinburgh3 papers (2019–2020)Yuanhua Huang · University of Edinburgh3 papers (2018–2020)Anna Cuomo · AstraZeneca (United Kingdom)3 papers (2019–2021)Aaron T. L. Lun · Walter and Eliza Hall Institute of Medical Research3 papers (2016–2016) · 2 papers (2018–2018)Petr Danecek · Wellcome Sanger Institute2 papers (2018–2020)Susan J. Clark · University of Sheffield2 papers (2018–2018)Na Cai · Helmholtz-Institute Ulm2 papers (2020–2020)Aaron E. Darling · University of California, Davis2 papers (2018–2018)Giordano Alvari · German Cancer Research Center2 papers (2021–2021)Thomas Quertermous · Cardiovascular Institute of the South2 papers (2020–2020)Matteo D’Antonio · University of Washington2 papers (2020–2020)David Jakubosky · University of California San Diego2 papers (2020–2020)Gordon K. Smyth · The University of Melbourne2 papers (2012–2013)Ludovic Vallier · Open Targets2 papers (2019–2019)Séan O’Donoghue · Commonwealth Scientific and Industrial Research Organisation2 papers (2018–2018)Yunshun Chen · Walter and Eliza Hall Institute of Medical Research2 papers (2012–2013)
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