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Description:

openTSNE 1.0.2

openTSNE is a modular Python implementation of t-Distributed Stochasitc Neighbor Embedding (t-SNE) [1], a popular dimensionality-reduction algorithm for visualizing high-dimensional data sets. openTSNE incorporates the latest improvements to the t-SNE algorithm, including the ability to add new data points to existing embeddings [2], massive speed improvements [3] [4] [5], enabling t-SNE to scale to millions of data points and various tricks to improve global alignment of the resulting visualizations [6].

A visualization of 44,808 single cell transcriptomes obtained from the mouse retina [7] embedded using the multiscale kernel trick to better preserve the global aligment of the clusters.

Documentation
User Guide and Tutorial
Examples: basic, advanced, preserving global alignment, embedding large data sets
Speed benchmarks

Installation
openTSNE requires Python 3.8 or higher in order to run.

Conda
openTSNE can be easily installed from conda-forge with
conda install --channel conda-forge opentsne
Conda package

PyPi
openTSNE is also available through pip and can be installed with
pip install opentsne
PyPi package

Installing from source
If you wish to install openTSNE from source, please run
pip install .
in the root directory to install the appropriate dependencies and compile the necessary binary files.
Please note that openTSNE requires a C/C++ compiler to be available on the system.
In order for openTSNE to utilize multiple threads, the C/C++ compiler
must support OpenMP. In practice, almost all compilers
implement this with the exception of older version of clang on OSX
systems.
To squeeze the most out of openTSNE, you may also consider installing
FFTW3 prior to installation. FFTW3 implements the Fast Fourier
Transform, which is heavily used in openTSNE. If FFTW3 is not available,
openTSNE will use numpy’s implementation of the FFT, which is slightly
slower than FFTW. The difference is only noticeable with large data sets
containing millions of data points.

A hello world example
Getting started with openTSNE is very simple. First, we’ll load up some data using scikit-learn
from sklearn import datasets

iris = datasets.load_iris()
x, y = iris["data"], iris["target"]
then, we’ll import and run
from openTSNE import TSNE

embedding = TSNE().fit(x)

Citation
If you make use of openTSNE for your work we would appreciate it if you would cite the paper
@article{Policar2024,
title={openTSNE: A Modular Python Library for t-SNE Dimensionality Reduction and Embedding},
author={Poli{\v c}ar, Pavlin G. and Stra{\v z}ar, Martin and Zupan, Bla{\v z}},
journal={Journal of Statistical Software},
year={2024},
volume={109},
number={3},
pages={1–30},
doi={10.18637/jss.v109.i03},
url={https://www.jstatsoft.org/index.php/jss/article/view/v109i03}
}
openTSNE implements two efficient algorithms for t-SNE. Please consider citing the original authors of the algorithm that you use. If you use FIt-SNE (default), then the citation is [5] below, but if you use Barnes-Hut the citations are [3] and [4].

References

[1]
Van Der Maaten, Laurens, and Hinton, Geoffrey. “Visualizing data using
t-SNE.”
Journal of Machine Learning Research 9.Nov (2008): 2579-2605.

[2]
Poličar, Pavlin G., Martin Stražar, and Blaž Zupan. “Embedding to Reference t-SNE Space Addresses Batch Effects in Single-Cell Classification.” Machine Learning (2021): 1-20.

[3]
(1,2)
Van Der Maaten, Laurens. “Accelerating t-SNE using tree-based algorithms.”
Journal of Machine Learning Research 15.1 (2014): 3221-3245.

[4]
(1,2)
Yang, Zhirong, Jaakko Peltonen, and Samuel Kaski. “Scalable optimization of neighbor embedding for visualization.” International Conference on Machine Learning. PMLR, 2013.

[5]
(1,2)
Linderman, George C., et al. “Fast interpolation-based t-SNE for improved
visualization of single-cell RNA-seq data.” Nature Methods 16.3 (2019): 243.

[6]
Kobak, Dmitry, and Berens, Philipp. “The art of using t-SNE for single-cell transcriptomics.”
Nature Communications 10, 5416 (2019).

[7]
Macosko, Evan Z., et al. “Highly parallel genome-wide expression profiling of
individual cells using nanoliter droplets.”
Cell 161.5 (2015): 1202-1214.