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Nathan Skene
Nathan Skene
Lecturer ; UKRI Future Leaders Fellow ; UK DRI group leader at the UK Dementia Research Institute
在 imperial.ac.uk 的电子邮件经过验证 - 首页
标题
引用次数
年份
Predicting cell type-specific epigenomic profiles accounting for distal genetic effects
AE Murphy, W Beardall, M Rei, M Phuycharoen, NG Skene
bioRxiv, 2024.02. 15.580484, 2024
2024
rworkflows: automating reproducible practices for the R community
BM Schilder, AE Murphy, NG Skene
Nature Communications 15 (1), 149, 2024
2024
Predicting gene expression from histone marks using chromatin deep learning models depends on histone mark function, regulatory distance and cellular states
AE Murphy, A Askarova, BE Lenhard, NG Skene, SJ Marzi
bioRxiv, 2024.03. 29.587323, 2024
2024
Avoiding false discoveries in single-cell RNA-seq by revisiting the first Alzheimer’s disease dataset
AE Murphy, N Fancy, N Skene
Elife 12, RP90214, 2023
12023
Artificial intelligence for dementia genetics and omics
C Bettencourt, N Skene, S Bandres‐Ciga, E Anderson, LM Winchester, ...
Alzheimer's & Dementia 19 (12), 5905-5921, 2023
92023
Harnessing the potential of machine learning and artificial intelligence for dementia research
JM Ranson, M Bucholc, D Lyall, D Newby, L Winchester, NP Oxtoby, ...
Brain Informatics 10 (1), 6, 2023
132023
miR-483-5p offsets functional and behavioural effects of stress in male mice through synapse-targeted repression of Pgap2 in the basolateral amygdala
M Mucha, AE Skrzypiec, JB Kolenchery, V Brambilla, S Patel, ...
Nature Communications 14 (1), 2134, 2023
62023
Avoiding false discoveries: Revisiting an Alzheimer’s disease snRNA-Seq dataset
AE Murphy, NN Fancy, NG Skene
bioRxiv, 2023.04. 01.535040, 2023
22023
Single-cell mRNA-regulation analysis reveals cell type-specific mechanisms of type 2 diabetes
JA Martínez-López, A Lindqvist, A Lopez-Pascual, P Chen, L Shcherbina, ...
bioRxiv, 2023.03. 23.533985, 2023
2023
Transcriptomic analyses reveal neuronal specificity of Leigh syndrome associated genes
A Wahedi, C Soondram, AE Murphy, N Skene, S Rahman
Journal of Inherited Metabolic Disease 46 (2), 243-260, 2023
42023
Identification of cell type-specific gene targets underlying thousands of rare diseases and subtraits
KB Murphy, R Gordon-Smith, J Chapman, M Otani, BM Schilder, ...
medRxiv, 2023.02. 13.23285820, 2023
2023
The rworkflows suite: automated continuous integration for quality checking, documentation website creation, and containerised deployment of R packages
BM Schilder, AE Murphy, NG Skene
2023
EpiCompare: R package for the comparison and quality control of epigenomic peak files
S Choi, BM Schilder, L Abbasova, AE Murphy, NG Skene
Bioinformatics Advances 3 (1), vbad049, 2023
2023
Reply to: A balanced measure shows superior performance of pseudobulk methods in single-cell RNA-sequencing analysis
KD Zimmerman, C Evans, CD Langefeld
Nature communications 13 (1), 7852, 2022
232022
The Deep Dementia Phenotyping (DEMON) Network: A global platform for innovation using data science and artificial intelligence
JM Ranson, AA Khleifat, DM Lyall, D Newby, LM Winchester, P Proitsi, ...
Alzheimer's & Dementia 18, e067873, 2022
2022
The Emerging Role of AI in Dementia Research and Healthcare
JM Ranson, M Bucholc, D Lyall, D Newby, L Winchester, N Oxtoby, ...
Artificial Intelligence in Healthcare: Recent Applications and Developments …, 2022
2022
CELL-AND TISSUE-TYPE ENRICHMENT TESTING BASED ON GENETIC ASSOCIATION STUDIES
A McIntosh, Y Lu, N Skene
European Neuropsychopharmacology 63, e35, 2022
2022
CUT&Tag recovers up to half of ENCODE ChIP-seq peaks in modifications of H3K27
D Hu, L Abbasova, BM Schilder, A Nott, NG Skene, SJ Marzi
bioRxiv, 2022.03. 30.486382, 2022
22022
A balanced measure shows superior performance of pseudobulk methods over mixed models and pseudoreplication approaches in single-cell RNA-sequencing analysis
AE Murphy, NG Skene
bioRxiv, 2022.02. 16.480517, 2022
22022
Multidimensional dynamics of the proteome in the neurodegenerative and aging mammalian brain
B Andrews, AE Murphy, M Stofella, S Maslen, L Almeida-Souza, ...
Molecular & Cellular Proteomics 21 (2), 2022
72022
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