Evidence map›Paper›PMID 38553996›Full record

ArticleStatistics in medicine2024

Information-incorporated sparse hierarchical cancer heterogeneity analysis.

Wei Han, Sanguo Zhang, Shuangge Ma, Mingyang Ren

Abstract read
In one paragraph

Article in Statistics in medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Wei HanSchool of Mathematical Sciences, University of Chinese Academy of Sciences, Beijing, China.ORCID 0009-0004-1344-9365
Sanguo ZhangSchool of Mathematical Sciences, University of Chinese Academy of Sciences, Beijing, China.
Shuangge MaDepartment of Biostatistics, Yale School of Public Health, New Haven, Connecticut.ORCID 0000-0001-9001-4999
Mingyang RenSchool of Mathematical Sciences, Shanghai Jiao Tong University, Shanghai, China.ORCID 0000-0002-8061-9940

Funding

Novel methods for identifying genetic interactions in cancer prognosisR01CA204120 · NCI · YALE UNIVERSITY · PI Shuangge Ma · 2016 to 2026
$3.5M
National Natural Science Foundation of China 12171454National Science Foundation 2209685NCI NIH HHS R01 CA204120NIH HHS CA204120
6 · The paper itself

Abstract

Cancer heterogeneity analysis is essential for precision medicine. Most of the existing heterogeneity analyses only consider a single type of data and ignore the possible sparsity of important features. In cancer clinical practice, it has been suggested that two types of data, pathological imaging and omics data, are commonly collected and can produce hierarchical heterogeneous structures, in which the refined sub-subgroup structure determined by omics features can be nested in the rough subgroup structure determined by the imaging features. Moreover, sparsity pursuit has extraordinary significance and is more challenging for heterogeneity analysis, because the important features may not be the same in different subgroups, which is ignored by the existing heterogeneity analyses. Fortunately, rich information from previous literature (for example, those deposited in PubMed) can be used to assist feature selection in the present study. Advancing from the existing analyses, in this study, we propose a novel sparse hierarchical heterogeneity analysis framework, which can integrate two types of features and incorporate prior knowledge to improve feature selection. The proposed approach has satisfactory statistical properties and competitive numerical performance. A TCGA real data analysis demonstrates the practical value of our approach in analyzing data heterogeneity and sparsity.

Indexed as

NeoplasmsComputer SimulationGenetic HeterogeneityHumansModels, StatisticalPrecision Medicinedata integrationfeature selectionheterogeneity analysishierarchyprior information

Identifiers

PMID38553996
PMCPMC12201913

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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.