Evidence map›Paper›PMID 25592847›Full record

ArticleBMC bioinformatics2015

Semi-supervised adaptive-height snipping of the hierarchical clustering tree.

Askar Obulkasim, Gerrit A Meijer, Mark A van de Wiel

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Article in BMC bioinformatics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Askar ObulkasimDepartment of Epidemiology and Biostatistics, VU University Medical Center, Amsterdam, The Netherlands. a.wubulikasimu@erasmusmc.nl.
Gerrit A MeijerDepartment of Pathology, VU University Medical Center, Amsterdam, The Netherlands. ga.meijer@vumc.nl.
Mark A van de WielDepartment of Epidemiology and Biostatistics, VU University Medical Center, Amsterdam, The Netherlands. mark.vdwiel@vumc.nl.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn genomics, hierarchical clustering (HC) is a popular method for grouping similar samples based on a distance measure. HC algorithms do not actually create clusters, but compute a hierarchical representation of the data set. Usually, a fixed height on the HC tree is used, and each contiguous branch of samples below that height is considered a separate cluster. Due to the fixed-height cutting, those clusters may not unravel significant functional coherence hidden deeper in the tree. Besides that, most existing approaches do not make use of available clinical information to guide cluster extraction from the HC. Thus, the identified subgroups may be difficult to interpret in relation to that information.

resultsWe develop a novel framework for decomposing the HC tree into clusters by semi-supervised piecewise snipping. The framework, called guided piecewise snipping, utilizes both molecular data and clinical information to decompose the HC tree into clusters. It cuts the given HC tree at variable heights to find a partition (a set of non-overlapping clusters) which does not only represent a structure deemed to underlie the data from which HC tree is derived, but is also maximally consistent with the supplied clinical data. Moreover, the approach does not require the user to specify the number of clusters prior to the analysis. Extensive results on simulated and multiple medical data sets show that our approach consistently produces more meaningful clusters than the standard fixed-height cut and/or non-guided approaches.

conclusionsThe guided piecewise snipping approach features several novelties and advantages over existing approaches. The proposed algorithm is generic, and can be combined with other algorithms that operate on detected clusters. This approach represents an advancement in several regards: (1) a piecewise tree snipping framework that efficiently extracts clusters by snipping the HC tree possibly at variable heights while preserving the HC tree structure; (2) a flexible implementation allowing a variety of data types for both building and snipping the HC tree, including patient follow-up data like survival as auxiliary information. The data sets and R code are provided as supplementary files. The proposed method is available from Bioconductor as the R-package HCsnip.

Indexed as

AlgorithmsCluster AnalysisData MiningDNA Copy Number VariationsGene Expression ProfilingGenomicsHumansNeoplasmsSurvival Analysis

Identifiers

PMID25592847
PMCPMC4302100

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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.