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Abstract
We present Vision, a tool for annotating the sources of variation in single cell RNA-seq data in an automated and scalable manner. Vision operates directly on the manifold of cell-cell similarity and employs a flexible annotation approach that can operate either with or without preconceived stratification of the cells into groups or along a continuum. We demonstrate the utility of Vision in several case studies and show that it can derive important sources of cellular variation and link them to experimental meta-data even with relatively homogeneous sets of cells. Vision produces an interactive, low latency and feature rich web-based report that can be easily shared among researchers, thus facilitating data dissemination and collaboration.
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1 Center for Computational Biology, University of California Berkeley, Berkeley, CA, USA
2 Biological and Medical Informatics Graduate Program, University of California, San Francisco, CA, USA
3 Department of Epidemiology and Biostatistics, Department of Bioengineering and Therapeutic Sciences, Institute for Human Genetics, University of California, San Francisco, CA, USA
4 Department of Electrical Engineering and Computer Science and Center for Computational Biology, University of California, Berkeley, Berkeley, CA, USA; Ragon Institute of Massachusetts General Hospital, MIT and Harvard, Cambridge, MA, USA; Chan-Zuckerberg Biohub, San Francisco, CA, USA