Alicia Oshlack

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Gordon K SmythDivision Head, Bioinformatics, Walter and Eliza Hall Institute of Medical ResearchEmail verificata su wehi.edu.au
Belinda PhipsonLaboratory Head, The Walter and Eliza Hall Institute of Medical ResearchEmail verificata su wehi.edu.au
Jovana MaksimovicSenior Researcher, Peter MacCallum Cancer CentreEmail verificata su petermac.org
Nadia M DavidsonWalter and Eliza Hall InstituteEmail verificata su unimelb.edu.au
Luke ZappiaHelmholtz Zentrum München/Technische Universität MünchenEmail verificata su helmholtz-muenchen.de
Matthew D YoungWellcome Sanger InstituteEmail verificata su sanger.ac.uk
Matthew WakefieldWalter & Eliza Hall Institute; Dept of Obstetrics and Gynaecology, Univ of MelbourneEmail verificata su wehi.edu.au
Mark D. RobinsonFull Professor of Statistical Genomics, University of ZurichEmail verificata su mls.uzh.ch
Kynan LawlorMurdoch Childrens Research InstituteEmail verificata su mcri.edu.au
Yoav GiladUniversity of ChicagoEmail verificata su uchicago.edu
Alexander N CombesMonash Biomedicine Discovery Institute, Department of Anatomy and Developmental Biology, MonashEmail verificata su monash.edu
Andrew LonsdaleThe University of MelbourneEmail verificata su student.unimelb.edu.au
Blewitt ME, Blewitt M, Champ MELaboratory head, Walter and Eliza Hall InstituteEmail verificata su wehi.edu.au
Lavinia GordonUniversity of MelbourneEmail verificata su unimelb.edu.au
Matthew WhitingCSIRO Space & AstronomyEmail verificata su csiro.au
Lauren BrownResearch Officer, Children's Cancer InstituteEmail verificata su ccia.org.au
Matthew E RitchieThe Walter and Eliza Hall Institute of Medical ResearchEmail verificata su wehi.edu.au
richard safferyEmail verificata su mcri.edu.au
Rachel WebsterUniversity of MelbourneEmail verificata su unimelb.edu.au
Craig SmithAssociate Professor of Biology, Monash UniversityEmail verificata su monash.edu

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Alicia Oshlack

Peter MacCallum Cancer Centre

Email verificata su petermac.org - Home page

Bioinformatics RNA-seq scRNA-seq Cancer clinical genomics


Titolo Ordina per citazioni Ordina per anno Ordina per titolo	Citata da Citata da	Anno
A scaling normalization method for differential expression analysis of RNA-seq data MD Robinson, A Oshlack Genome biology 11, 1-9, 2010	8144	2010
Gene ontology analysis for RNA-seq: accounting for selection bias MD Young, MJ Wakefield, GK Smyth, A Oshlack Genome biology 11, 1-12, 2010	6386	2010
A comparison of background correction methods for two-colour microarrays ME Ritchie, J Silver, A Oshlack, M Holmes, D Diyagama, A Holloway, ... Bioinformatics 23 (20), 2700-2707, 2007	1143	2007
From RNA-seq reads to differential expression results A Oshlack, MD Robinson, MD Young Genome biology 11, 1-10, 2010	978	2010
SWAN: Subset-quantile within array normalization for illumina infinium HumanMethylation450 BeadChips J Maksimovic, L Gordon, A Oshlack Genome biology 13, 1-12, 2012	901	2012
Splatter: simulation of single-cell RNA sequencing data L Zappia, B Phipson, A Oshlack Genome biology 18 (1), 174, 2017	797	2017
missMethyl: an R package for analyzing data from Illumina’s HumanMethylation450 platform B Phipson, J Maksimovic, A Oshlack Bioinformatics 32 (2), 286-288, 2015	699	2015
Transcript length bias in RNA-seq data confounds systems biology A Oshlack, MJ Wakefield Biology direct 4, 1-10, 2009	683	2009
Corset: enabling differential gene expression analysis for de novoassembled transcriptomes NM Davidson, A Oshlack Genome biology 15, 1-14, 2014	650	2014
Clustering trees: a visualization for evaluating clusterings at multiple resolutions L Zappia, A Oshlack Gigascience 7 (7), giy083, 2018	628	2018
A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders Z Stark, TY Tan, B Chong, GR Brett, P Yap, M Walsh, A Yeung, H Peters, ... Genetics in medicine 18 (11), 1090-1096, 2016	412	2016
Expression profiling in primates reveals a rapid evolution of human transcription factors Y Gilad, A Oshlack, GK Smyth, TP Speed, KP White Nature 440 (7081), 242-245, 2006	396	2006
ChIP-seq analysis reveals distinct H3K27me3 profiles that correlate with transcriptional activity MD Young, TA Willson, MJ Wakefield, E Trounson, DJ Hilton, ME Blewitt, ... Nucleic acids research 39 (17), 7415-7427, 2011	352	2011
Disorders of sex development: insights from targeted gene sequencing of a large international patient cohort S Eggers, S Sadedin, JA Van Den Bergen, G Robevska, T Ohnesorg, ... Genome biology 17, 1-21, 2016	342	2016
Diagnostic impact and cost-effectiveness of whole-exome sequencing for ambulant children with suspected monogenic conditions TY Tan, OJ Dillon, Z Stark, D Schofield, K Alam, R Shrestha, B Chong, ... JAMA pediatrics 171 (9), 855-862, 2017	322	2017
Array-based gene discovery with three unrelated subjects shows SCARB2/LIMP-2 deficiency causes myoclonus epilepsy and glomerulosclerosis SF Berkovic, LM Dibbens, A Oshlack, JD Silver, M Katerelos, DF Vears, ... The American Journal of Human Genetics 82 (3), 673-684, 2008	311	2008
Exploring the single-cell RNA-seq analysis landscape with the scRNA-tools database L Zappia, B Phipson, A Oshlack PLoS computational biology 14 (6), e1006245, 2018	298	2018
Optimizing the noise versus bias trade-off for Illumina whole genome expression BeadChips W Shi, A Oshlack, GK Smyth Nucleic acids research 38 (22), e204-e204, 2010	268	2010
Natural selection on gene expression Y Gilad, A Oshlack, SA Rifkin TRENDS in Genetics 22 (8), 456-461, 2006	258	2006
Evaluation of variability in human kidney organoids B Phipson, PX Er, AN Combes, TA Forbes, SE Howden, L Zappia, HJ Yen, ... Nature methods 16 (1), 79-87, 2019	224	2019

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