Integrative analysis of single-cell genomics data by coupled nonnegative matrix factorizations
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Yong Wang | Wing Hung Wong | Howard Y. Chang | Xi Chen | Mahdi Zamanighomi | Zhana Duren | Wanwen Zeng | Ansuman T Satpathy | Howard Y Chang | Ansuman T. Satpathy | W. Wong | Mahdi Zamanighomi | Yong Wang | Wanwen Zeng | Zhana Duren | Xi Chen | W. Wong
[1] Colin N. Dewey,et al. RSEM: accurate transcript quantification from RNA-Seq data with or without a reference genome , 2011, BMC Bioinformatics.
[2] Thomas R. Gingeras,et al. STAR: ultrafast universal RNA-seq aligner , 2013, Bioinform..
[3] Clifford A. Meyer,et al. Model-based Analysis of ChIP-Seq (MACS) , 2008, Genome Biology.
[4] A. Oshlack,et al. Splatter: simulation of single-cell RNA sequencing data , 2017, Genome Biology.
[5] William J. Greenleaf,et al. chromVAR: Inferring transcription factor-associated accessibility from single-cell epigenomic data , 2017, Nature Methods.
[6] Alicia N. Schep,et al. Unsupervised clustering and epigenetic classification of single cells , 2017, Nature Communications.
[7] Steffen Bickel,et al. Multi-view clustering , 2004, Fourth IEEE International Conference on Data Mining (ICDM'04).
[8] Howard Y. Chang,et al. Single-cell chromatin accessibility reveals principles of regulatory variation , 2015, Nature.
[9] M. Schaub,et al. SC3 - consensus clustering of single-cell RNA-Seq data , 2016, Nature Methods.
[10] George M. Church,et al. Biclustering of Expression Data , 2000, ISMB.
[11] Rhonda Bacher,et al. Design and computational analysis of single-cell RNA-sequencing experiments , 2016, Genome Biology.
[12] Howard Y. Chang,et al. Lineage-specific and single cell chromatin accessibility charts human hematopoiesis and leukemia evolution , 2016, Nature Genetics.
[13] Bing Ren,et al. Systematic mapping of chromatin state landscapes during mouse development , 2017, bioRxiv.
[14] P. Kharchenko,et al. Integrative single-cell analysis of transcriptional and epigenetic states in the human adult brain , 2017, Nature Biotechnology.
[15] Aviv Regev,et al. Massively-parallel single nucleus RNA-seq with DroNc-seq , 2017, Nature Methods.
[16] Catalin C. Barbacioru,et al. mRNA-Seq whole-transcriptome analysis of a single cell , 2009, Nature Methods.
[17] Pablo Tamayo,et al. Metagenes and molecular pattern discovery using matrix factorization , 2004, Proceedings of the National Academy of Sciences of the United States of America.
[18] Phillip C. Yang,et al. In vitro differentiation of mouse embryonic stem (mES) cells using the hanging drop method. , 2008, Journal of visualized experiments : JoVE.
[19] Michael W. Berry,et al. Algorithms and applications for approximate nonnegative matrix factorization , 2007, Comput. Stat. Data Anal..
[20] Aaron R. Quinlan,et al. Bioinformatics Applications Note Genome Analysis Bedtools: a Flexible Suite of Utilities for Comparing Genomic Features , 2022 .
[21] ENCODEConsortium,et al. An Integrated Encyclopedia of DNA Elements in the Human Genome , 2012, Nature.
[22] Juan Liu,et al. A novel computational framework for simultaneous integration of multiple types of genomic data to identify microRNA-gene regulatory modules , 2011, Bioinform..
[23] O. Stegle,et al. Single-Cell Genome-Wide Bisulfite Sequencing for Assessing Epigenetic Heterogeneity , 2014, Nature Methods.
[24] M Maden,et al. Retinoic acid and development of the central nervous system , 1992, BioEssays : news and reviews in molecular, cellular and developmental biology.
[25] J. Hartigan. Direct Clustering of a Data Matrix , 1972 .
[26] W. Wong,et al. Modeling gene regulation from paired expression and chromatin accessibility data , 2017, Proceedings of the National Academy of Sciences.
[27] Data production leads,et al. An integrated encyclopedia of DNA elements in the human genome , 2012 .
[28] N. Friedman,et al. Chromatin state dynamics during blood formation , 2014, Science.
[29] Michael D. Schneider,et al. Endogenous retinoic acid regulates cardiac progenitor differentiation , 2010, Proceedings of the National Academy of Sciences.