Oliver Stegle researcher
Stegle, Oliver
VIAF ID: 1286157282921303640007 (Personal)
Permalink: http://viaf.org/viaf/1286157282921303640007
Preferred Forms
- 100 0 _ ‡a Oliver Stegle ‡c researcher
- 100 1 _ ‡a Stegle, Oliver
4xx's: Alternate Name Forms (3)
5xx's: Related Names (4)
- 510 2 _ ‡a Deutsches Krebsforschungszentrum ‡4 affi ‡4 https://d-nb.info/standards/elementset/gnd#affiliation ‡e Affiliation
- 510 2 _ ‡a European Molecular Biology Laboratory ‡4 affi ‡4 https://d-nb.info/standards/elementset/gnd#affiliation ‡e Affiliation
- 551 _ _ ‡a Heidelberg ‡4 ortw ‡4 https://d-nb.info/standards/elementset/gnd#placeOfActivity
- 510 2 _ ‡a University of Cambridge ‡4 affi ‡4 https://d-nb.info/standards/elementset/gnd#affiliation ‡e Affiliation
Works
Title | Sources |
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Cell segmentation-free inference of cell types from in situ transcriptomics data | |
Establishing highly multiplexed microfluidic screening of protein-antibody interactions | |
Framework and baseline examination of the German National Cohort (NAKO) | |
Genomic Rearrangements in Arabidopsis Considered as Quantitative Traits | |
Genotype-environment interactions reveal causal pathways that mediate genetic effects on phenotype | |
Germline determinants of the somatic mutation landscape in 2,642 cancer genomes | |
The germline genetic component of drug sensitivity in cancer cell lines | |
GWAS for executive function and processing speed suggests involvement of the CADM2 gene. | |
The Human Cell Atlas | |
IceR improves proteome coverage and data completeness in global and single-cell proteomics | |
Identifying extrinsic versus intrinsic drivers of variation in cell behaviour in human iPS cell lines from healthy donors | |
Inference algorithms and learning theory for Bayesian sparse factor analysis | |
An integrated map of structural variation in 2,504 human genomes | |
Integrative genome-wide analysis of the determinants of RNA splicing in kidney renal clear cell carcinoma | |
Interactions between genetic variation and cellular environment in skeletal muscle gene expression. | |
It is all in the noise: Efficient multi-task Gaussian process inference with structured residuals | |
Joint genetic analysis of gene expression data with inferred cellular phenotypes | |
Joint genetic analysis using variant sets reveals polygenic gene-context interactions | |
Joint modelling of confounding factors and prominent genetic regulators provides increased accuracy in genetical genomics studies | |
The Kipoi repository accelerates community exchange and reuse of predictive models for genomics | |
KMgene: a unified R package for gene-based association analysis for complex traits. | |
LifeTime and improving European healthcare through cell-based interceptive medicine | |
LIMIX: genetic analysis of multiple traits | |
LiMMBo: a simple, scalable approach for linear mixed models in high-dimensional genetic association studies | |
Lineage-Specific Genome Architecture Links Enhancers and Non-coding Disease Variants to Target Gene Promoters | |
A linear mixed model approach to study multivariate gene-environment interactions | |
Methods for Epigenetic Analyses from Long-Read Sequencing Data | |
Modeling Cell-Cell Interactions from Spatial Molecular Data with Spatial Variance Component Analysis | |
Modelling local gene networks increases power to detect trans-acting genetic effects on gene expression | |
MOFA+: a statistical framework for comprehensive integration of multi-modal single-cell data | |
Multi-omics Characterization of Interaction-mediated Control of Human Protein Abundance levels | |
Multi-Omics Factor Analysis-a framework for unsupervised integration of multi-omics data sets. | |
Multi-omics profiling of mouse gastrulation at single-cell resolution | |
Multi-tissue DNA methylation age predictor in mouse | |
Naive Pluripotent Stem Cells Exhibit Phenotypic Variability that Is Driven by Genetic Variation | |
OME-Zarr: a cloud-optimized bioimaging file format with international community support | |
omicsPrint: DETECTION OF DATA LINKAGE ERRORS IN MULTIPLE OMICS STUDIES. | |
An omnibus test for differential distribution analysis of microbiome sequencing data | |
Open Targets: a platform for therapeutic target identification and validation | |
The Organoid Cell Atlas: A Rosetta Stone for Biomedical Discovery and Regenerative Therapy | |
Patterns of cis regulatory variation in diverse human populations | |
Personalized medicine: from genotypes, molecular phenotypes and the quantified self, towards improved medicine. | |
Platelet function is modified by common sequence variation in megakaryocyte super enhancers | |
The Polygenic and Monogenic Basis of Blood Traits and Diseases | |
Population-scale proteome variation in human induced pluripotent stem cells | |
Population-scale single-cell RNA-seq profiling across dopaminergic neuron differentiation | |
Predicting and understanding the stability of G-quadruplexes | |
Probabilistic latent variable models for distinguishing between cause and effect | |
Promoter shape varies across populations and affects promoter evolution and expression noise. | |
Properties of structural variants and short tandem repeats associated with gene expression and complex traits | |
A random forest approach to capture genetic effects in the presence of population structure | |
Reply | |
A robust Bayesian two-sample test for detecting intervals of differential gene expression in microarray time series | |
Robustness and applicability of transcription factor and pathway analysis tools on single-cell RNA-seq data | |
scDALI: modeling allelic heterogeneity in single cells reveals context-specific genetic regulation | |
scNMT-seq enables joint profiling of chromatin accessibility DNA methylation and transcription in single cells. | |
Screening for genes that accelerate the epigenetic aging clock in humans reveals a role for the H3K36 methyltransferase NSD1 | |
scRNA-seq assessment of the human lung, spleen, and esophagus tissue stability after cold preservation | |
Selenzyme: Enzyme selection tool for pathway design. | |
ShapePheno: unsupervised extraction of shape phenotypes from biological image collections. | |
Single-cell Atlas of common variable immunodeficiency shows germinal center-associated epigenetic dysregulation in B-cell responses | |
Single-cell epigenomics: Recording the past and predicting the future. | |
The single-cell eQTLGen consortium | |
Single-cell genome-wide bisulfite sequencing for assessing epigenetic heterogeneity | |
Single cell multi-omics profiling reveals a hierarchical epigenetic landscape during mammalian germ layer specification: Supplementary Figures | |
Single-cell RNA-sequencing of differentiating iPS cells reveals dynamic genetic effects on gene expression | |
SpatialDE: identification of spatially variable genes | |
Spontaneous epigenetic variation in the Arabidopsis thaliana methylome. | |
Statistical Tests for Detecting Differential RNA-Transcript Expression from Read Counts | |
Structural rearrangements generate cell-specific, gene-independent CRISPR-Cas9 loss of fitness effects | |
Structured data abstractions and interpretable latent representations for single-cell multimodal genomics | |
Systematic genetic analysis of the MHC region reveals mechanistic underpinnings of HLA type associations with disease | |
Temporal mixture modelling of single-cell RNA-seq data resolves a CD4+ T cell fate bifurcation | |
Transcriptome and genome sequencing uncovers functional variation in humans | |
UC2 search: Using unique connectivity of uncharged compounds for metabolite annotation by database searching in mass spectrometry-based metabolomics. | |
Unraveling the polygenic architecture of complex traits using blood eQTL meta-analysis | |
Using probabilistic estimation of expression residuals (PEER) to obtain increased power and interpretability of gene expression analyses | |
Using the past to estimate sensory uncertainty | |
Vireo: Bayesian demultiplexing of pooled single-cell RNA-seq data without genotype reference | |
Vitamin A-Retinoic Acid Signaling Regulates Hematopoietic Stem Cell Dormancy. | |
Warped linear mixed models for the genetic analysis of transformed phenotypes | |
Warped Matrix Factorisation for Multi-view Data Integration | |
Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits | |
Whole-genome sequencing of multiple Arabidopsis thaliana populations. | |
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