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Nucleic Acids Research|December 6, 2014
Allele-specific copy number profiling by next-generation DNA sequencingHao Chen, John M Bell, Nicolas A Zavala, et al.Genome Biology|November 28, 2018
CODEX2: full-spectrum copy number variation detection by high-throughput DNA sequencingYuchao Jiang, Rujin Wang, Eugene Urrutia, et al.Nature Methods|September 1, 2019
Data denoising with transfer learning in single-cell transcriptomicsJingshu Wang, Divyansh Agarwal, Mo Huang, et al.Gigascience|July 9, 2018
SVEngine: an efficient and versatile simulator of genome structural variations with features of cancer clonal evolutionLi Charlie Xia, Dongmei Ai, Hojoon Lee, et al.Elife|April 26, 2021
A Mendelian randomization study of the role of lipoprotein subfractions in coronary artery diseaseQingyuan Zhao, Jingshu Wang, Zhen Miao, et al.Plos Genetics|June 22, 2021
Causal inference for heritable phenotypic risk factors using heterogeneous genetic instrumentsJingshu Wang, Qingyuan Zhao, Jack Bowden, et al.Bioinformatics (Oxford, England)|November 19, 2015
Global copy number profiling of cancer genomesXuefeng Wang, Mengjie Chen, Xiaoqing Yu, et al.Nucleic Acids Research|November 30, 2017
Identification of large rearrangements in cancer genomes with barcode linked readsLi C Xia, John M Bell, Christina Wood-Bouwens, et al.Proceedings of the National Academy of Sciences of the United States of America|June 28, 2018
Gene expression distribution deconvolution in single-cell RNA sequencingJingshu Wang, Mo Huang, Eduardo Torre, et al.Nature Biotechnology|May 21, 2021
Integrative single-cell analysis of allele-specific copy number alterations and chromatin accessibility in cancerChi-Yun Wu, Billy T Lau, Heon Seok Kim, et al.Pageof 10