Nancy R. Zhang, Ph.D.
Affiliations: | 2005 | Stanford University, Palo Alto, CA |
Area:
Statistics, Biostatistics BiologyGoogle:
"Nancy Zhang"Parents
Sign in to add mentorDavid O. Siegmund | grad student | 2005 | Stanford | |
(Change -point detection and sequence alignment: Statistical problems of genomics.) |
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Publications
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Zhou Z, Xu B, Minn A, et al. (2020) DENDRO: genetic heterogeneity profiling and subclone detection by single-cell RNA sequencing. Genome Biology. 21: 10 |
Agarwal D, Wang J, Zhang NR. (2020) Data Denoising and Post-Denoising Corrections in Single Cell RNA Sequencing Statistical Science. 35: 112-128 |
Agarwal D, Zhang NR. (2019) Semblance: An empirical similarity kernel on probability spaces. Science Advances. 5: eaau9630 |
Jiang Y, Wang R, Urrutia E, et al. (2018) CODEX2: full-spectrum copy number variation detection by high-throughput DNA sequencing. Genome Biology. 19: 202 |
Zhou Z, Wang W, Wang LS, et al. (2018) Integrative DNA copy number detection and genotyping from sequencing and array-based platforms. Bioinformatics (Oxford, England). 34: 2349-2355 |
Xia LC, Ai D, Lee H, et al. (2018) SVEngine: an efficient and versatile simulator of genome structural variations with features of cancer clonal evolution. Gigascience |
Wang J, Huang M, Torre E, et al. (2018) Gene expression distribution deconvolution in single-cell RNA sequencing. Proceedings of the National Academy of Sciences of the United States of America |
Huang M, Wang J, Torre E, et al. (2018) SAVER: gene expression recovery for single-cell RNA sequencing. Nature Methods |
Urrutia E, Chen H, Zhou Z, et al. (2018) Integrative pipeline for profiling DNA copy number and inferring tumor phylogeny. Bioinformatics (Oxford, England) |
Xia LC, Bell JM, Wood-Bouwens C, et al. (2017) Identification of large rearrangements in cancer genomes with barcode linked reads. Nucleic Acids Research |