ArticleBMC bioinformatics2017
Divisive hierarchical maximum likelihood clustering.
Article in BMC bioinformatics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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.
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.
Who cites it
5 citing papers in PubMed.
- A Real-World Cross-Sectional Study on Suspected Mast Cell Activation Syndrome: Multiple Heterogeneous Symptoms Identified.Clinical and translational allergy · 2026Article
- A divisive hierarchical clustering methodology for enhancing the ensemble prediction power in large scale population studies: the ATHLOS project.Health information science and systems · 2022Article
- K-Module Algorithm: An Additional Step to Improve the Clustering Results of WGCNA Co-Expression Networks.Genes · 2021Article
- Disentangling the Association of Hydroxychloroquine Treatment with Mortality in Covid-19 Hospitalized Patients through Hierarchical Clustering.Journal of healthcare engineering · 2021Article
- A bioinformatics potpourri.BMC genomics · 2018Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundBiological data comprises various topologies or a mixture of forms, which makes its analysis extremely complicated. With this data increasing in a daily basis, the design and development of efficient and accurate statistical methods has become absolutely necessary. Specific analyses, such as those related to genome-wide association studies and multi-omics information, are often aimed at clustering sub-conditions of cancers and other diseases. Hierarchical clustering methods, which can be categorized into agglomerative and divisive, have been widely used in such situations. However, unlike agglomerative methods divisive clustering approaches have consistently proved to be computationally expensive.
resultsThe proposed clustering algorithm (DRAGON) was verified on mutation and microarray data, and was gauged against standard clustering methods in the literature. Its validation included synthetic and significant biological data. When validated on mixed-lineage leukemia data, DRAGON achieved the highest clustering accuracy with data of four different dimensions. Consequently, DRAGON outperformed previous methods with 3-,4- and 5-dimensional acute leukemia data. When tested on mutation data, DRAGON achieved the best performance with 2-dimensional information.
conclusionsThis work proposes a computationally efficient divisive hierarchical clustering method, which can compete equally with agglomerative approaches. The proposed method turned out to correctly cluster data with distinct topologies. A MATLAB implementation can be extraced from http://www.riken.jp/en/research/labs/ims/med_sci_math/ or http://www.alok-ai-lab.com.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.