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Nancy Ruonan Zhang
Nancy Ruonan Zhang
Verifierad e-postadress på wharton.upenn.edu
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Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project
Management Group Liefer Laura A. 51 Wetterstrand Kris A. 51 Good Peter J. 51 ...
nature 447 (7146), 799-816, 2007
59292007
SAVER: gene expression recovery for single-cell RNA sequencing
M Huang, J Wang, E Torre, H Dueck, S Shaffer, R Bonasio, JI Murray, ...
Nature methods 15 (7), 539-542, 2018
6402018
Bulk tissue cell type deconvolution with multi-subject single-cell expression reference
X Wang, J Park, K Susztak, NR Zhang, M Li
Nature communications 10 (1), 380, 2019
6262019
Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications
DF Levinson, J Duan, S Oh, K Wang, AR Sanders, J Shi, N Zhang, ...
American Journal of Psychiatry 168 (3), 302-316, 2011
4862011
A modified Bayes information criterion with applications to the analysis of comparative genomic hybridization data
NR Zhang, DO Siegmund
Biometrics 63 (1), 22-32, 2007
4682007
The Human Tumor Atlas Network: charting tumor transitions across space and time at single-cell resolution
O Rozenblatt-Rosen, A Regev, P Oberdoerffer, T Nawy, A Hupalowska, ...
Cell 181 (2), 236-249, 2020
3702020
Opposing Functions of Interferon Coordinate Adaptive and Innate Immune Responses to Cancer Immune Checkpoint Blockade
JL Benci, LR Johnson, R Choa, Y Xu, J Qiu, Z Zhou, B Xu, D Ye, ...
Cell 178 (4), 933-948. e14, 2019
3392019
BRCA locus-specific loss of heterozygosity in germline BRCA1 and BRCA2 carriers
KN Maxwell, B Wubbenhorst, BM Wenz, D De Sloover, J Pluta, L Emery, ...
Nature communications 8 (1), 1-11, 2017
2702017
Assessing intratumor heterogeneity and tracking longitudinal and spatial clonal evolutionary history by next-generation sequencing
Y Jiang, Y Qiu, AJ Minn, NR Zhang
Proceedings of the National Academy of Sciences 113 (37), E5528-E5537, 2016
2392016
Bayesian variable selection in structured high-dimensional covariate spaces with applications in genomics
F Li, NR Zhang
Journal of the American statistical association 105 (491), 1202-1214, 2010
2332010
Detecting simultaneous changepoints in multiple sequences
NR Zhang, DO Siegmund, H Ji, JZ Li
Biometrika 97 (3), 631-645, 2010
2082010
Graph-based change-point detection
H Chen, N Zhang
The Annals of Statistics 43 (1), 139-176, 2015
1972015
Ultrasensitive detection of rare mutations using next-generation targeted resequencing
P Flaherty, G Natsoulis, O Muralidharan, M Winters, J Buenrostro, J Bell, ...
Nucleic acids research 40 (1), e2-e2, 2012
1742012
CODEX: a normalization and copy number variation detection method for whole exome sequencing
Y Jiang, DA Oldridge, SJ Diskin, NR Zhang
Nucleic acids research 43 (6), e39-e39, 2015
1672015
Data denoising with transfer learning in single-cell transcriptomics
J Wang, D Agarwal, M Huang, G Hu, Z Zhou, C Ye, NR Zhang
Nature methods 16 (9), 875-878, 2019
1622019
The Alzheimer's disease sequencing project: study design and sample selection
GW Beecham, JC Bis, ER Martin, SH Choi, AL DeStefano, CM Van Duijn, ...
Neurology Genetics 3 (5), 2017
1372017
Metastatic tumor evolution and organoid modeling implicate TGFBR2 as a cancer driver in diffuse gastric cancer
LD Nadauld, S Garcia, G Natsoulis, JM Bell, L Miotke, ES Hopmans, H Xu, ...
Genome biology 15 (8), 1-18, 2014
1362014
Gene expression distribution deconvolution in single-cell RNA sequencing
J Wang, M Huang, E Torre, H Dueck, S Shaffer, J Murray, A Raj, M Li, ...
Proceedings of the National Academy of Sciences 115 (28), E6437-E6446, 2018
1222018
Whole‐exome sequencing in 20,197 persons for rare variants in Alzheimer's disease
NS Raghavan, AM Brickman, H Andrews, JJ Manly, N Schupf, R Lantigua, ...
Annals of clinical and translational neurology 5 (7), 832-842, 2018
1152018
Detecting simultaneous variant intervals in aligned sequences
D Siegmund, B Yakir, NR Zhang
The Annals of Applied Statistics 5 (2A), 645-668, 2011
1042011
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Artiklar 1–20