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      SCALE method for single-cell ATAC-seq analysis via latent feature extraction

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          Abstract

          Single-cell ATAC-seq (scATAC-seq) profiles the chromatin accessibility landscape at single cell level, thus revealing cell-to-cell variability in gene regulation. However, the high dimensionality and sparsity of scATAC-seq data often complicate the analysis. Here, we introduce a method for analyzing scATAC-seq data, called Single-Cell ATAC-seq analysis via Latent feature Extraction (SCALE). SCALE combines a deep generative framework and a probabilistic Gaussian Mixture Model to learn latent features that accurately characterize scATAC-seq data. We validate SCALE on datasets generated on different platforms with different protocols, and having different overall data qualities. SCALE substantially outperforms the other tools in all aspects of scATAC-seq data analysis, including visualization, clustering, and denoising and imputation. Importantly, SCALE also generates interpretable features that directly link to cell populations, and can potentially reveal batch effects in scATAC-seq experiments.

          Abstract

          Single-cell ATAC-seq data is challenging to analyse for reasons such as high dimensionality and sparsity. Here, the authors develop SCALE, a deep learning method that leverages latent feature extraction for various tasks of scATACseq data analysis.

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          Most cited references12

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          Proposals for the Classification of the Acute Leukaemias French-American-British (FAB) Co-operative Group

          A uniform system of classification and nomenclature of the acute leukaemias, at present lacking, should permit more accurate recording of the distribution of cases entered into clinical trials, and could provide a reference standard when newly developed cell-surface markers believed to characterize specific cell types are applied to cases of acute leukaemia. Proposals based on conventional morphological and cytochemical methods are offered following the study of peripheral blood and bone-marrow films from some 200 cases of acute leukaemia by a group of seven French, American and British haematologists. The slides were examined first independently, and then by the group working together. Two groups of acute leukaemia, 'lymphoblastic' and myeloid are further subdivided into three and six groups. Dysmyelopoietic syndromes that may be confused with acute myeloid leukaemia are also considered. Photomicrographs of each of the named conditions are presented.
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            Visualizing data using ti-SNE

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              SAVER: Gene expression recovery for single-cell RNA sequencing

              In single-cell RNA sequencing (scRNA-seq) studies, only a small fraction of the transcripts present in each cell are sequenced. This leads to unreliable quantification of lowly and moderately expressed genes which hinders downstream analysis. To address this challenge, we introduce SAVER (Single-cell Analysis Via Expression Recovery), an expression recovery method for UMI-based scRNA-seq data that borrows information across genes and cells to obtain accurate expression estimates for all genes.
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                Author and article information

                Contributors
                qczhang@tsinghua.edu.cn
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                8 October 2019
                8 October 2019
                2019
                : 10
                : 4576
                Affiliations
                [1 ]ISNI 0000 0001 0662 3178, GRID grid.12527.33, MOE Key Laboratory of Bioinformatics, Beijing Advanced Innovation Center for Structural Biology, Center for Synthetic and Systems Biology, Tsinghua-Peking Center for Life Sciences, School of Life Sciences, , Tsinghua University, ; 100084 Beijing, China
                [2 ]ISNI 0000 0001 2256 9319, GRID grid.11135.37, Beijing Advanced Innovation Center for Genomics (ICG), Biomedical Pioneering Innovation Center (BIOPIC), , Peking University, ; 100871 Beijing, China
                [3 ]ISNI 0000 0001 2256 9319, GRID grid.11135.37, State Key Laboratory of Protein and Plant Gene Research, School of Life Sciences, Center for Bioinformatics, , Peking University, ; 100871 Beijing, China
                [4 ]ISNI 0000 0001 0662 3178, GRID grid.12527.33, Bioinformatics Division, BNRist, Department of Automation, , Tsinghua University, ; 100084 Beijing, China
                [5 ]ISNI 0000 0001 2151 7939, GRID grid.267323.1, Department of Biological Sciences, Center for Systems Biology, , The University of Texas, ; Dallas 800 West Campbell Road, RL11, Richardson, TX 75080-3021 USA
                [6 ]ISNI 0000 0001 0662 3178, GRID grid.12527.33, MOE Key Laboratory of Bioinformatics, Center for Synthetic and Systems Biology, School of Medicine, , Tsinghua University, ; 100084 Beijing, China
                [7 ]ISNI 0000 0001 2222 1582, GRID grid.266097.c, Department of Computer Science and Engineering, , University of California, ; Riverside, CA 92521 USA
                [8 ]ISNI 0000 0001 0662 3178, GRID grid.12527.33, Bioinformatics Division, BNRIST; Department of Computer Science and Technology, , Tsinghua University, ; 100084 Beijing, China
                Author information
                http://orcid.org/0000-0002-2392-114X
                http://orcid.org/0000-0003-3833-4498
                http://orcid.org/0000-0002-4913-0338
                Article
                12630
                10.1038/s41467-019-12630-7
                6783552
                31594952
                362efd6b-553c-4754-9fc8-6490c4f23e49
                © The Author(s) 2019

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 26 February 2019
                : 20 September 2019
                Funding
                Funded by: FundRef https://doi.org/10.13039/501100002855, Ministry of Science and Technology of the People's Republic of China (Chinese Ministry of Science and Technology);
                Award ID: 2018YFA0107603
                Award Recipient :
                Funded by: FundRef https://doi.org/10.13039/501100001809, National Natural Science Foundation of China (National Science Foundation of China);
                Award ID: 91740204
                Award ID: 31761163007
                Award ID: 31621063
                Award Recipient :
                Categories
                Article
                Custom metadata
                © The Author(s) 2019

                Uncategorized
                functional clustering,epigenomics,chromatin,chromatin structure
                Uncategorized
                functional clustering, epigenomics, chromatin, chromatin structure

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