Paper detail

Comparison of Clustering Methods for Time Course Genomic Data: Applications to Aging Effects

Time course microarray data provide insight about dynamic biological processes. While several clustering methods have been proposed for the analysis of these data structures, comparison and selection of appropriate clustering methods are seldom discussed. We compared $3$ probabilistic based clustering methods and $3$ distance based clustering methods for time course microarray data. Among probabilistic methods, we considered: smoothing spline clustering also known as model based functional data analysis (MFDA), functional clustering models for sparsely sampled data (FCM) and model-based clustering (MCLUST). Among distance based methods, we considered: weighted gene co-expression network analysis (WGCNA), clustering with dynamic time warping distance (DTW) and clustering with autocorrelation based distance (ACF). We studied these algorithms in both simulated settings and case study data. Our investigations showed that FCM performed very well when gene curves were short and sparse. DTW and WGCNA performed well when gene curves were medium or long ($>=10$ observations). SSC performed very well when there were clusters of gene curves similar to one another. Overall, ACF performed poorly in these applications. In terms of computation time, FCM, SSC and DTW were considerably slower than MCLUST and WGCNA. WGCNA outperformed MCLUST by generating more accurate and biological meaningful clustering results. WGCNA and MCLUST are the best methods among the 6 methods compared, when performance and computation time are both taken into account. WGCNA outperforms MCLUST, but MCLUST provides model based inference and uncertainty measure of clustering results.

preprint2014arXivOpen access
0citations
0reviews
0saves
Nocode
Nodataset
0institutions

Next steps

Decide what to do with this paper

Use like or dislike for the fast social read. The more specific scholarly feedback stays available below when needed.

Log in to curate

Reading frame

Keep the important context close to the paper

Keep the important signals around this paper in one place: votes, save state, collection context, reviews and the metadata you need before deciding what to do next.

Institutions

Add specific reaction

Move through the context

Research map

Open full explorer

Move through nearby people, institutions, topics and adjacent work without leaving the paper page.

Building this graph slice

BZPEER is loading the nearby papers, people, topics and institutions for this page.

Structured reviews

0 review(s)

ContributeLeave structured feedbackUse the review template when you have a concrete strength, concern or method question.Open review form

No structured reviews yet. High-signal critique starts here.

Work discussion

0 comment(s)

DiscussAdd a high-signal commentKeep quick notes, caveats and replication pointers separate from formal reviews.Open comment form

No discussion yet. The first strong comment sets the tone.