PhEMD
"PhEMD" (Phenotypic Earth Mover's Distance) is a computational method to identify axes of variation among multicellular biospecimens profiled at single-cell resolution. Recognizing the gap in tools for analyzing variation among complex biospecimens rather than individual cells, PhEMD introduces a unique approach by embedding a "manifold of manifolds," where each datapoint in the higher-level manifold represents a collection of points within a lower-level manifold of cells.
Key Features and Functionalities:
- Identification of Axes of Variation: PhEMD is tailored to uncover axes of subpopulational variation among biospecimens under various perturbation conditions, enriching our understanding of complex biological and clinical phenomena.
- Inference of Unprofiled Phenotypes: A distinctive feature of PhEMD is its ability to infer the phenotypes of biospecimens that have not been directly profiled, providing valuable insights into potential biological states based on existing data.
- Application to Clinical Datasets: When applied to clinical datasets, PhEMD can generate a map of patient-state space, illuminating sources of variation from one patient to another and potentially uncovering novel aspects of disease mechanisms and patient responses.
- Scalability and Compatibility: PhEMD is designed to be scalable to large datasets, ensuring its applicability in high-throughput experiments. It is also compatible with leading batch-effect correction techniques, making it versatile across different experimental designs.
- Generalizability: The method is generalizable to multiple experimental designs, offering flexibility for researchers in diverse biological and clinical research fields.
Topic
Genotype and phenotype;Oncology;Cytometry;Sample collections;RNA-Seq
Detail
Operation: Deisotoping;Regression analysis;Clustering
Software interface: Command-line interface
Language: R
License: GNU General Public License, version 2
Cost: Free with restrictions
Version name: 1.15.1
Credit: The Chan-Zuckerberg Initiative, the Swiss National Science Foundation, the European Research Council, and the National Institutes of Health (NIH).
Input: -
Output: -
Contact: Bernd Bodenmiller bernd.bodenmiller@imls.uzh.ch ,Smita Krishnaswamy smita.krishnaswamy@yale.edu
Collection: -
Maturity: Stable
Publications
- Uncovering axes of variation among single-cell cancer specimens.
- Chen WS, et al. Uncovering axes of variation among single-cell cancer specimens. Uncovering axes of variation among single-cell cancer specimens. 2020; 17:302-310. doi: 10.1038/s41592-019-0689-z
- https://doi.org/10.1038/S41592-019-0689-Z
- PMID: 31932777
- PMC: PMC7339867
Download and documentation
Source: https://github.com/wschen/phemd
Documentation: https://github.com/KrishnaswamyLab/phemd/blob/master/README.md
Home page: https://github.com/wschen/phemd
Links: https://github.com/KrishnaswamyLab/phemd/tree/master/vignettes
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