PT - JOURNAL ARTICLE AU - Kevin R. Moon AU - David van Dijk AU - Zheng Wang AU - Daniel Burkhardt AU - William S. Chen AU - Antonia van den Elzen AU - Matthew J. Hirn AU - Ronald R. Coifman AU - Natalia B. Ivanova AU - Guy Wolf AU - Smita Krishnaswamy TI - Visualizing Transitions and Structure for High Dimensional Data Exploration AID - 10.1101/120378 DP - 2017 Jan 01 TA - bioRxiv PG - 120378 4099 - http://biorxiv.org/content/early/2017/12/01/120378.short 4100 - http://biorxiv.org/content/early/2017/12/01/120378.full AB - In the era of ‘Big Data’ there is a pressing need for tools that provide human interpretable visualizations of emergent patterns in high-throughput high-dimensional data. Further, to enable insightful data exploration, such visualizations should faithfully capture and emphasize emergent structures and patterns without enforcing prior assumptions on the shape or form of the data. In this paper, we present PHATE (Potential of Heat-diffusion for Affinity-based Transition Embedding) - an unsupervised low-dimensional embedding for visualization of data that is aimed at solving these issues. Unlike previous methods that are commonly used for visualization, such as PCA and tSNE, PHATE is able to capture and highlight both local and global structure in the data. In particular, in addition to clustering patterns, PHATE also uncovers and emphasizes progression and transitions (when they exist) in the data, which are often missed in other visualization-capable methods. Such patterns are especially important in biological data that contain, for example, single-cell phenotypes at different phases of differentiation, patients at different stages of disease progression, and gut microbial compositions that vary gradually between individuals, even of the same enterotype.The embedding provided by PHATE is based on a novel informational distance that captures long-range nonlinear relations in the data by computing energy potentials of data-adaptive diffusion processes. We demonstrate the effectiveness of the produced visualization in revealing insights on a wide variety of biomedical data, including single-cell RNA-sequencing, mass cytometry, gut microbiome sequencing, human SNP data, Hi-C data, as well as non-biomedical data, such as facebook network and facial image data. In order to validate the capability of PHATE to enable exploratory analysis, we generate a new dataset of 31,000 single-cells from a human embryoid body differentiation system. Here, PHATE provides a comprehensive picture of the differentiation process, while visualizing major and minor branching trajectories in the data. We validate that all known cell types are recapitulated in the PHATE embedding in proper organization. Furthermore, the global picture of the system offered by PHATE allows us to connect parts of the developmental progression and characterize novel regulators associated with developmental lineages.