Oliver Stegle 个人学术档案

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引用	60572	46111
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John MarioniGenentech在 gene.com 的电子邮件经过验证
Karsten BorgwardtDirector, Max Planck Institute of Biochemistry在 biochem.mpg.de 的电子邮件经过验证
Wolf ReikHead, Epigenetics Programme, Babraham Institute Cambridge, UK在 babraham.ac.uk 的电子邮件经过验证
Sarah A. TeichmannWellcome Sanger Institute & University of Cambridge在 cam.ac.uk 的电子邮件经过验证
Christoph LippertProfessor, Hasso Plattner Institute, Universität Potsdam在 hpi.de 的电子邮件经过验证
Francesco Paolo CasaleHelmholtz Pioneer Campus, Institute of AI for Health, Helmholtz Zentrum München在 helmholtz-muenchen.de 的电子邮件经过验证
Marc Jan BonderPostdoctoral researcher UMCG在 umcg.nl 的电子邮件经过验证
Gunnar RätschProfessor, ETH Zürich在 inf.ethz.ch 的电子邮件经过验证
Leopold PartsFaculty at Wellcome Sanger Institute; Senior Researcher (part-time) at University of Tartu在 sanger.ac.uk 的电子邮件经过验证
Richard DurbinDept of Genetics, University of Cambridge在 cam.ac.uk 的电子邮件经过验证
Ricard ArgelaguetAltos Labs在 altoslabs.com 的电子邮件经过验证
Detlef WeigelMax Planck Institute for Biology Tübingen在 weigelworld.org 的电子邮件经过验证
John WinnPrincipal Researcher, Machine Learning Group, Microsoft Research Cambridge在 microsoft.com 的电子邮件经过验证
Neil D. LawrenceUniversity of Cambridge在 cl.cam.ac.uk 的电子邮件经过验证
Stephen ClarkBabraham Institute在 babraham.ac.uk 的电子邮件经过验证
Richard MottWeldon Professor of Computational Genetics, University College London, UK在 ucl.ac.uk 的电子邮件经过验证
Magnus NordborgGregor Mendel Institute, Austrian Academy of Sciences在 gmi.oeaw.ac.at 的电子邮件经过验证
Bernhard SchölkopfDirector, Max Planck Institute for Intelligent Systems & ELLIS Institute Tübingen; Professor at ETH在 tuebingen.mpg.de 的电子邮件经过验证
Ewan BirneyDirector, EMBL-EBI在 ebi.ac.uk 的电子邮件经过验证
David MacKayProfessor of Natural Philosophy, Cavendish Laboratory, University of Cambridge在 mrao.cam.ac.uk 的电子邮件经过验证

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Oliver Stegle

German Cancer Research Center (DKFZ) & EMBL Heidelberg

在 dkfz.de 的电子邮件经过验证 - 首页

Systems Genetics Single-cell genomics Computational Biology Statistical 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 global reference for human genetic variation 1000 Genomes Project Consortium Nature 526 (7571), 68, 2015	15036	2015
An integrated map of structural variation in 2,504 human genomes PH Sudmant, T Rausch, EJ Gardner, RE Handsaker, A Abyzov, ... Nature 526 (7571), 75-81, 2015	2395	2015
The human cell atlas A Regev, SA Teichmann, ES Lander, I Amit, C Benoist, E Birney, ... elife 6, e27041, 2017	2068	2017
Transcriptome and genome sequencing uncovers functional variation in humans T Lappalainen, M Sammeth, MR Friedländer, PAC ‘t Hoen, J Monlong, ... Nature 501 (7468), 506-511, 2013	2060	2013
Pan-cancer analysis of whole genomes Nature 578 (7793), 82-93, 2020	1805*	2020
Deep learning for computational biology C Angermueller, T Pärnamaa, L Parts, O Stegle Molecular systems biology 12 (7), 878, 2016	1537	2016
Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression U Võsa, A Claringbould, HJ Westra, MJ Bonder, P Deelen, B Zeng, ... Nature genetics 53 (9), 1300-1310, 2021	1306*	2021
Severe COVID-19 is marked by a dysregulated myeloid cell compartment J Schulte-Schrepping, N Reusch, D Paclik, K Baßler, S Schlickeiser, ... Cell 182 (6), 1419-1440. e23, 2020	1292	2020
Computational and analytical challenges in single-cell transcriptomics O Stegle, SA Teichmann, JC Marioni Nature Reviews Genetics 16 (3), 133-145, 2015	1266	2015
Computational analysis of cell-to-cell heterogeneity in single-cell RNA-sequencing data reveals hidden subpopulations of cells F Buettner, KN Natarajan, FP Casale, V Proserpio, A Scialdone, FJ Theis, ... Nature biotechnology 33 (2), 155-160, 2015	1240	2015
Single-cell genome-wide bisulfite sequencing for assessing epigenetic heterogeneity SA Smallwood, HJ Lee, C Angermueller, F Krueger, H Saadeh, J Peat, ... Nature methods 11 (8), 817-820, 2014	1137	2014
Whole-genome sequencing of multiple Arabidopsis thaliana populations J Cao, K Schneeberger, S Ossowski, T Günther, S Bender, J Fitz, ... Nature Genetics 43 (10), 956-963, 2011	1091	2011
Eleven grand challenges in single-cell data science D Lähnemann, J Köster, E Szczurek, DJ McCarthy, SC Hicks, ... Genome biology 21, 1-35, 2020	1002	2020
Lineage-specific genome architecture links enhancers and non-coding disease variants to target gene promoters BM Javierre, OS Burren, SP Wilder, R Kreuzhuber, SM Hill, S Sewitz, ... Cell 167 (5), 1369-1384. e19, 2016	988	2016
Using probabilistic estimation of expression residuals (PEER) to obtain increased power and interpretability of gene expression analyses O Stegle, L Parts, M Piipari, J Winn, R Durbin Nature protocols 7 (3), 500-507, 2012	975	2012
Multi‐Omics Factor Analysis—a framework for unsupervised integration of multi‐omics data sets R Argelaguet, B Velten, D Arnol, S Dietrich, T Zenz, JC Marioni, F Buettner, ... Molecular systems biology 14 (6), e8124, 2018	875	2018
A comprehensive assessment of RNA-seq accuracy, reproducibility and information content by the Sequencing Quality Control Consortium. SMIII Consortium Nature Biotechnology 32 (9), 903-914, 2014	849	2014
Spontaneous epigenetic variation in the Arabidopsis thaliana methylome C Becker, J Hagmann, J Müller, D Koenig, O Stegle, K Borgwardt, ... Nature 480 (7376), 245-249, 2011	771	2011
Multiple reference genomes and transcriptomes for Arabidopsis thaliana X Gan, O Stegle, J Behr, JG Steffen, P Drewe, KL Hildebrand, R Lyngsoe, ... Nature 477 (7365), 419-423, 2011	743	2011
Comprehensive analysis of alternative splicing across tumors from 8,705 patients A Kahles, KV Lehmann, NC Toussaint, M Hüser, SG Stark, ... Cancer cell 34 (2), 211-224. e6, 2018	736	2018

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