Alicia Oshlack 个人学术档案

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	总计	2019 年至今
引用	28854	18386
h 指数	57	48
i10 指数	101	92

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Gordon K SmythDivision Head, Bioinformatics, Walter and Eliza Hall Institute of Medical Research在 wehi.edu.au 的电子邮件经过验证
Belinda PhipsonLaboratory Head, The Walter and Eliza Hall Institute of Medical Research在 wehi.edu.au 的电子邮件经过验证
Jovana MaksimovicSenior Researcher, Peter MacCallum Cancer Centre在 petermac.org 的电子邮件经过验证
Nadia M DavidsonWalter and Eliza Hall Institute在 unimelb.edu.au 的电子邮件经过验证
Luke ZappiaHelmholtz Zentrum München/Technische Universität München在 helmholtz-muenchen.de 的电子邮件经过验证
Matthew D YoungWellcome Sanger Institute在 sanger.ac.uk 的电子邮件经过验证
Matthew WakefieldWalter & Eliza Hall Institute; Dept of Obstetrics and Gynaecology, Univ of Melbourne在 wehi.edu.au 的电子邮件经过验证
Mark D. RobinsonFull Professor of Statistical Genomics, University of Zurich在 mls.uzh.ch 的电子邮件经过验证
Kynan LawlorMurdoch Childrens Research Institute在 mcri.edu.au 的电子邮件经过验证
Yoav GiladUniversity of Chicago在 uchicago.edu 的电子邮件经过验证
Alexander N CombesMonash Biomedicine Discovery Institute, Department of Anatomy and Developmental Biology, Monash在 monash.edu 的电子邮件经过验证
Andrew LonsdaleThe University of Melbourne在 student.unimelb.edu.au 的电子邮件经过验证
Blewitt ME, Blewitt M, Champ MELaboratory head, Walter and Eliza Hall Institute在 wehi.edu.au 的电子邮件经过验证
Lavinia GordonUniversity of Melbourne在 unimelb.edu.au 的电子邮件经过验证
Matthew WhitingCSIRO Space & Astronomy在 csiro.au 的电子邮件经过验证
Matthew E RitchieThe Walter and Eliza Hall Institute of Medical Research在 wehi.edu.au 的电子邮件经过验证
richard saffery在 mcri.edu.au 的电子邮件经过验证
Rachel WebsterUniversity of Melbourne在 unimelb.edu.au 的电子邮件经过验证
Craig SmithAssociate Professor of Biology, Monash University在 monash.edu 的电子邮件经过验证
Harriet DashnowUniversity of Utah在 genetics.utah.edu 的电子邮件经过验证

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Alicia Oshlack

Peter MacCallum Cancer Centre

在 petermac.org 的电子邮件经过验证 - 首页

Bioinformatics RNA-seq scRNA-seq Cancer clinical genomics


标题按引用次数排序按年份排序按标题排序	引用次数引用次数	年份
A scaling normalization method for differential expression analysis of RNA-seq data MD Robinson, A Oshlack Genome biology 11, 1-9, 2010	7765	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	6138	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	1131	2007
From RNA-seq reads to differential expression results A Oshlack, MD Robinson, MD Young Genome biology 11, 1-10, 2010	957	2010
SWAN: Subset-quantile within array normalization for illumina infinium HumanMethylation450 BeadChips J Maksimovic, L Gordon, A Oshlack Genome biology 13, 1-12, 2012	885	2012
Splatter: simulation of single-cell RNA sequencing data L Zappia, B Phipson, A Oshlack Genome biology 18 (1), 174, 2017	744	2017
Transcript length bias in RNA-seq data confounds systems biology A Oshlack, MJ Wakefield Biology direct 4, 1-10, 2009	665	2009
missMethyl: an R package for analyzing data from Illumina’s HumanMethylation450 platform B Phipson, J Maksimovic, A Oshlack Bioinformatics 32 (2), 286-288, 2015	653	2015
Corset: enabling differential gene expression analysis for de novoassembled transcriptomes NM Davidson, A Oshlack Genome biology 15, 1-14, 2014	606	2014
Clustering trees: a visualization for evaluating clusterings at multiple resolutions L Zappia, A Oshlack Gigascience 7 (7), giy083, 2018	531	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	400	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	394	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	341	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	319	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	310	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	305	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	282	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	260	2010
Natural selection on gene expression Y Gilad, A Oshlack, SA Rifkin TRENDS in Genetics 22 (8), 456-461, 2006	247	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	213	2019

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