Evidence map›Paper›PMID 34293851›Full record

ArticleBriefings in bioinformatics2021

Supervised clustering of high-dimensional data using regularized mixture modeling.

Wennan Chang, Changlin Wan, Yong Zang, Chi Zhang, Sha Cao

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Article
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  4. Generalized Matrix Local Low Rank Representation by Random Projection and Submatrix Propagation.KDD : proceedings. International Conference on Knowledge Discovery & Data Mining · 2023
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Wennan ChangDepartment of Electrical and Computer Engineering, Purdue University.
Changlin WanDepartment of Electrical and Computer Engineering, Purdue University.
Yong ZangDepartment of Biostatistics and a member of the Center for Computational Biology and Bioinformatics, Indiana University School of Medicine.
Chi ZhangDepartment of Medical and Molecular Genetics and a member of the Center for Computational Biology and Bioinformatics, Indiana University School of Medicine.
Sha CaoDepartment of Biostatistics and a member of the Center for Computational Biology and Bioinformatics, Indiana University School of Medicine.

Funding

Construction of cell specific gene co-regulations signatures based on single cell transcriptomics analysisR01GM131399 · NIGMS · SOUTH DAKOTA STATE UNIVERSITY · PI MA, QIN · 2018 to 2021
$1.3M
NIGMS NIH HHS #1R01GM131399-01NIGMS NIH HHS R01 GM131399
6 · The paper itself

Abstract

Identifying relationships between genetic variations and their clinical presentations has been challenged by the heterogeneous causes of a disease. It is imperative to unveil the relationship between the high-dimensional genetic manifestations and the clinical presentations, while taking into account the possible heterogeneity of the study subjects.We proposed a novel supervised clustering algorithm using penalized mixture regression model, called component-wise sparse mixture regression (CSMR), to deal with the challenges in studying the heterogeneous relationships between high-dimensional genetic features and a phenotype. The algorithm was adapted from the classification expectation maximization algorithm, which offers a novel supervised solution to the clustering problem, with substantial improvement on both the computational efficiency and biological interpretability. Experimental evaluation on simulated benchmark datasets demonstrated that the CSMR can accurately identify the subspaces on which subset of features are explanatory to the response variables, and it outperformed the baseline methods. Application of CSMR on a drug sensitivity dataset again demonstrated the superior performance of CSMR over the others, where CSMR is powerful in recapitulating the distinct subgroups hidden in the pool of cell lines with regards to their coping mechanisms to different drugs. CSMR represents a big data analysis tool with the potential to resolve the complexity of translating the clinical representations of the disease to the real causes underpinning it. We believe that it will bring new understanding to the molecular basis of a disease and could be of special relevance in the growing field of personalized medicine.

Indexed as

AlgorithmsGenetic VariationModels, GeneticHumansdisease heterogeneitymixture modelingsupervised learning

Identifiers

PMID34293851
PMCPMC8294591

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Registered trials

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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.