Wei Wang
Wei Wang
Ph.D. in Computer Science, New Jersey Institute of Technology
Підтверджена електронна адреса в njit.edu - Домашня сторінка
De novo mutations in histone-modifying genes in congenital heart disease
S Zaidi, M Choi, H Wakimoto, L Ma, J Jiang, JD Overton, ...
Nature 498 (7453), 220-223, 2013
Low concordance of multiple variant-calling pipelines: practical implications for exome and genome sequencing
J O'Rawe, T Jiang, G Sun, Y Wu, W Wang, J Hu, P Bodily, L Tian, ...
Genome medicine 5 (3), 1-18, 2013
SNVer: a statistical tool for variant calling in analysis of pooled or individual next-generation sequencing data
Z Wei, W Wang, P Hu, GJ Lyon, H Hakonarson
Nucleic acids research 39 (19), e132-e132, 2011
Dysregulation of synaptogenesis genes antecedes motor neuron pathology in spinal muscular atrophy
Z Zhang, AM Pinto, L Wan, W Wang, MG Berg, I Oliva, LN Singh, ...
Proceedings of the National Academy of Sciences 110 (48), 19348-19353, 2013
Large sample size, wide variant spectrum, and advanced machine-learning technique boost risk prediction for inflammatory bowel disease
Z Wei, W Wang, J Bradfield, J Li, C Cardinale, E Frackelton, C Kim, ...
The American Journal of Human Genetics 92 (6), 1008-1012, 2013
The SLE transcriptome exhibits evidence of chronic endotoxin exposure and has widespread dysregulation of non-coding and coding RNAs
L Shi, Z Zhang, MY Angela, W Wang, Z Wei, E Akhter, K Maurer, PC Reis, ...
PloS one 9 (5), e93846, 2014
Exome sequencing and unrelated findings in the context of complex disease research: ethical and clinical implications
GJ Lyon, T Jiang, R Van Wijk, W Wang, PM Bodily, J Xing, L Tian, ...
Discovery medicine 12 (62), 41, 2011
Minor introns are embedded molecular switches regulated by highly unstable U6atac snRNA
I Younis, K Dittmar, W Wang, SW Foley, MG Berg, KY Hu, Z Wei, L Wan, ...
Elife 2, e00780, 2013
A change-point model for identifying 3′ UTR switching by next-generation RNA sequencing
W Wang, Z Wei, H Li
Bioinformatics 30 (15), 2162-2170, 2014
An empirical Bayes testing procedure for detecting variants in analysis of next generation sequencing data
Z Zhao, W Wang, Z Wei
The Annals of Applied Statistics, 2229-2248, 2013
SNVerGUI: a desktop tool for variant analysis of next-generation sequencing data
W Wang, W Hu, F Hou, P Hu, Z Wei
Journal of medical genetics 49 (12), 753-755, 2012
Low concordance of multiple variant-calling pipelines: practical implications for exome and genome sequencing. Genome Med. 2013; 5: 28
J O’Rawe, T Jiang, G Sun, Y Wu, W Wang, J Hu, P Bodily, L Tian, ...
External Resources Pubmed/Medline (NLM) CrossRef (DOI), 0
Collapsing singletons may boost signal for associating rare variants in sequencing study
W Wang, Z Wei
BMC proceedings 8 (1), 1-4, 2014
Simultaneous set-wise testing under dependence, with applications to genome-wide association studies
W Sun, W Wang, Z Wei
Statistics and its Interface 3 (4), 501-511, 2010
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