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Biometrics|April 1, 2018
Sensitivity analysis and power for instrumental variable studiesXuran Wang, Yang Jiang, Nancy R Zhang, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 31, 2016
Assessing intratumor heterogeneity and tracking longitudinal and spatial clonal evolutionary history by next-generation sequencingYuchao Jiang, Yu Qiu, Andy J Minn, et al.
Frontiers in Genetics|March 6, 2023
Destin2: Integrative and cross-modality analysis of single-cell chromatin accessibility dataPeter Y Guan, Jin Seok Lee, Lihao Wang, et al.
Nature Communications|January 24, 2019
Bulk tissue cell type deconvolution with multi-subject single-cell expression referenceXuran Wang, Jihwan Park, Katalin Susztak, et al.
Bioinformatics (Oxford, England)|February 8, 2018
Integrative pipeline for profiling DNA copy number and inferring tumor phylogenyEugene Urrutia, Hao Chen, Zilu Zhou, et al.
Nucleic Acids Research|January 26, 2015
CODEX: a normalization and copy number variation detection method for whole exome sequencingYuchao Jiang, Derek A Oldridge, Sharon J Diskin, et al.
Biometrika|July 24, 2012
Detecting simultaneous changepoints in multiple sequencesNancy R Zhang, David O Siegmund, Hanlee Ji, et al.
NPJ Breast Cancer|November 28, 2017
Functional germline variants as potential co-oncogenesDivyansh Agarwal, Christoph Nowak, Nancy R Zhang, et al.
Nucleic Acids Research|October 17, 2017
Accounting for technical noise in differential expression analysis of single-cell RNA sequencing dataCheng Jia, Yu Hu, Derek Kelly, et al.
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