Evidence map›Paper›PMID 37710192›Full record

ArticleBMC bioinformatics2023

Scellpam: an R package/C++ library to perform parallel partitioning around medoids on scRNAseq data sets.

Juan Domingo, Teresa Leon, Esther Dura

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Article in BMC bioinformatics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Juan DomingoDepartment of Informatics, ETSE, University of Valencia, Avda. de la Universidad, s/n, 46100, Burjassot, Valencia, Spain. Juan.Domingo@uv.es.
Teresa LeonDepartment of Statistics and Operations Research, University of Valencia, Avda. Vicente Andres Estelles, 46100, Burjassot, Valencia, Spain.
Esther DuraDepartment of Informatics, ETSE, University of Valencia, Avda. de la Universidad, s/n, 46100, Burjassot, Valencia, Spain.

Funding

Spanish Ministry of Science and Education, MCIN/ AEI/10.13039/501100011033/ I+D+i funded project PGC type B with reference PID2020-117114GB-I00
6 · The paper itself

Abstract

backgroundPartitioning around medoids (PAM) is one of the most widely used and successful clustering method in many fields. One of its key advantages is that it only requires a distance or a dissimilarity between the individuals, and the fact that cluster centers are actual points in the data set means they can be taken as reliable representatives of their classes. However, its wider application is hampered by the large amount of memory needed to store the distance matrix (quadratic on the number of individuals) and also by the high computational cost of computing such distance matrix and, less importantly, by the cost of the clustering algorithm itself.

resultsTherefore, new software has been provided that addresses these issues. This software, provided under GPL license and usable as either an R package or a C++ library, calculates in parallel the distance matrix for different distances/dissimilarities ([Formula: see text], [Formula: see text], Pearson, cosine and weighted Euclidean) and also implements a parallel fast version of PAM (FASTPAM1) using any data type to reduce memory usage. Moreover, the parallel implementation uses all the cores available in modern computers which greatly reduces the execution time. Besides its general application, the software is especially useful for processing data of single cell experiments. It has been tested in problems including clustering of single cell experiments with up to 289,000 cells with the expression of about 29,000 genes per cell.

conclusionsComparisons with other current packages in terms of execution time have been made. The method greatly outperforms the available R packages for distance matrix calculation and also improves the packages that implement the PAM itself. The software is available as an R package at https://CRAN.R-project.org/package=scellpam and as C++ libraries at https://github.com/JdMDE/jmatlib and https://github.com/JdMDE/ppamlib The package is useful for single cell RNA-seq studies but it is also applicable in other contexts where clustering of large data sets is required.

Indexed as

Single-Cell Gene Expression AnalysisSoftwareAlgorithmsCluster AnalysisGene LibraryHumansDissimilarity matrixLarge datasetsParallel implementationPartitioning around medoidsSingle-cell RNA-seq analysis

Identifiers

PMID37710192
PMCPMC10503022

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.