Enhancing Clustering of Single-Cell RNA-Seq Data by Proximity Learning on Random Projected Spaces

Vrahatis, A. G., Dimitrakopoulos, G. N., Tasoulis, S. K., & Plagianakos, V. P. (2019). Enhancing Clustering of Single-Cell RNA-Seq Data by Proximity Learning on Random Projected Spaces. In 2019 IEEE 19th International Conference on Bioinformatics and Bioengineering (BIBE) (pp. 846–849). IEEE. https://doi.org/10.1109/bibe.2019.00157

Περίληψη

We are in the era of single-cell RNA sequencing technology, which offers a great potential for uncovering cellular differences with a higher resolution, shedding light in various complex biological processes and complex human diseases. However, such studies create extremely high dimensional data isolating expression profiles for thousands or even millions of cells. Consequently, dealing with single-cell RNA-seq (scRNA-seq) data is considered the main challenge for unsupervised clustering, which can be used in order to identify grouped cell types. Towards this direction, we present a framework that enhances hierarchical clustering utilizing Proximity Learning on Random Projected spaces (PLRP). The proposed method's efficiency lies in the fact that we exploit the distances from multiple significantly lower dimension spaces defined by Random Projections using ensembles of k-nearest neighbor searches. In the transformed data we applied hierarchical agglomerative clustering (HAC) improving significantly its performance when compared against using the original space. The performance of the proposed PLRP was evaluated in a publicly available experimental dataset with scRNA-seq expression profiles, against three well-established clustering tools. The results showed that our approach greatly enhances clustering performance exposing its applicability in ultra-high dimensions and imposing further development towards this direction.

DOI
10.1109/bibe.2019.00157
Τύπος
Άρθρο σε Πρακτικά Συνεδρίου
Έτος
2019

Σύνδεσμοι

BibTeX

@inproceedings{vrahatis2019enhancing,
title = {Enhancing Clustering of Single-Cell RNA-Seq Data by Proximity Learning on Random Projected Spaces},
author = {Aristidis G. Vrahatis and Georgios N. Dimitrakopoulos and Sotiris K. Tasoulis and Vassilis P. Plagianakos},
url = {https://doi.org/10.1109/bibe.2019.00157},
doi = {10.1109/bibe.2019.00157},
year  = {2019},
date = {2019-01-01},
booktitle = {2019 IEEE 19th International Conference on Bioinformatics and Bioengineering (BIBE)},
volume = {3},
pages = {846–849},
publisher = {IEEE},
abstract = {We are in the era of single-cell RNA sequencing technology, which offers a great potential for uncovering cellular differences with a higher resolution, shedding light in various complex biological processes and complex human diseases. However, such studies create extremely high dimensional data isolating expression profiles for thousands or even millions of cells. Consequently, dealing with single-cell RNA-seq (scRNA-seq) data is considered the main challenge for unsupervised clustering, which can be used in order to identify grouped cell types. Towards this direction, we present a framework that enhances hierarchical clustering utilizing Proximity Learning on Random Projected spaces (PLRP). The proposed method's efficiency lies in the fact that we exploit the distances from multiple significantly lower dimension spaces defined by Random Projections using ensembles of k-nearest neighbor searches. In the transformed data we applied hierarchical agglomerative clustering (HAC) improving significantly its performance when compared against using the original space. The performance of the proposed PLRP was evaluated in a publicly available experimental dataset with scRNA-seq expression profiles, against three well-established clustering tools. The results showed that our approach greatly enhances clustering performance exposing its applicability in ultra-high dimensions and imposing further development towards this direction.},
keywords = {},
pubstate = {published},
tppubtype = {inproceedings}
}

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