ArticlePloS one2015
Assessing Dissimilarity Measures for Sample-Based Hierarchical Clustering of RNA Sequencing Data Using Plasmode Datasets.
Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.
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13 citing papers in PubMed.
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- Transcriptomic Analysis in Human Macrophages Infected with Therapeutic Failure Clinical Isolates ofACS infectious diseases · 2022Article
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- Insights Into the Albinism Mechanism for Two Distinct Color Morphs of Northern Snakehead,Frontiers in genetics · 2020Article
- Subject level clustering using a negative binomial model for small transcriptomic studies.BMC bioinformatics · 2018Article
- Visual Pattern-Driven Exploration of Big Data.2018 International Symposium on Big Data Visual and Immersive Analytics (BDVA) : Konstanz, Germany, October 17 -19, 2018. IEEE International Symposium on Big Data Visual and Immersive Analytics (4th : 2018 : Konstanz, Germany) · 2018Article
- An integrated genomic analysis of anaplastic meningioma identifies prognostic molecular signatures.Scientific reports · 2018Article
- Silhouette Scores for Arbitrary Defined Groups in Gene Expression Data and Insights into Differential Expression Results.Biological procedures online · 2018Article
- Machine learning for epigenetics and future medical applications.Epigenetics · 2017Review
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3 authors.
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Abstract
Sample- and gene-based hierarchical cluster analyses have been widely adopted as tools for exploring gene expression data in high-throughput experiments. Gene expression values (read counts) generated by RNA sequencing technology (RNA-seq) are discrete variables with special statistical properties, such as over-dispersion and right-skewness. Additionally, read counts are subject to technology artifacts as differences in sequencing depth. This possesses a challenge to finding distance measures suitable for hierarchical clustering. Normalization and transformation procedures have been proposed to favor the use of Euclidean and correlation based distances. Additionally, novel model-based dissimilarities that account for RNA-seq data characteristics have also been proposed. Adequacy of dissimilarity measures has been assessed using parametric simulations or exemplar datasets that may limit the scope of the conclusions. Here, we propose the simulation of realistic conditions through creation of plasmode datasets, to assess the adequacy of dissimilarity measures for sample-based hierarchical clustering of RNA-seq data. Consistent results were obtained using plasmode datasets based on RNA-seq experiments conducted under widely different conditions. Dissimilarity measures based on Euclidean distance that only considered data normalization or data standardization were not reliable to represent the expected hierarchical structure. Conversely, using either a Poisson-based dissimilarity or a rank correlation based dissimilarity or an appropriate data transformation, resulted in dendrograms that resemble the expected hierarchical structure. Plasmode datasets can be generated for a wide range of scenarios upon which dissimilarity measures can be evaluated for sample-based hierarchical clustering analysis. We showed different ways of generating such plasmodes and applied them to the problem of selecting a suitable dissimilarity measure. We report several measures that are satisfactory and the choice of a particular measure may rely on the availability on the software pipeline of preference.
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