Evidence map›Paper›PMID 28018994›Full record

ArticleMedical image computing and computer-assisted intervention : MICCAI ... International Conference on Medical Image Computing and Computer-Assisted Intervention2016

Integrative Analysis of Cellular Morphometric Context Reveals Clinically Relevant Signatures in Lower Grade Glioma.

Ju Han, Yunfu Wang, Weidong Cai, Alexander Borowsky, Bahram Parvin, Hang Chang

Open access · greenAbstract read
In one paragraph

Article in Medical image computing and computer-assisted intervention : MICCAI ... International Conference on Medical Image Computing and Computer-Assisted Intervention, 2016. 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
2.7field-weighted citation impact, top 10% of its field
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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Article
  3. Unsupervised Transfer Learning via Multi-Scale Convolutional Sparse Coding for Biomedical Applications.IEEE transactions on pattern analysis and machine intelligence · 2018
    Article
4 · The record

Corrections and comments

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

6 authors at 4 institutions in 2 countries.

Ju HanLawrence Berkeley National Laboratory, Berkeley, California, U.S.A; Department of Electrical and Biomedical Engineering, University of Nevada, Reno, U.S.A.
Yunfu WangLawrence Berkeley National Laboratory, Berkeley, California, U.S.A; Department of Neurology, Taihe Hospital, Hubei University of Medicine, Hubei, China.
Weidong CaiSchool of Information Technologies, University of Sydney, Sydney, NSW, Australia.
Alexander BorowskyCenter for Comparative Medicine, University of California, Davis, California, U.S.A.
Bahram ParvinLawrence Berkeley National Laboratory, Berkeley, California, U.S.A; Department of Electrical and Biomedical Engineering, University of Nevada, Reno, U.S.A.
Hang ChangLawrence Berkeley National Laboratory, Berkeley, California, U.S.A; Department of Electrical and Biomedical Engineering, University of Nevada, Reno, U.S.A.
Lawrence Berkeley National Laboratory · USUniversity of Nevada, Reno · USUniversity of California, Davis · USUniversity of Sydney · AU

Funding

Molecular and Therapeutic Basis of Morphometric Aberrations in Brain TumorsR01CA184476 · NCI · UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB · PI CHANG, HANG · 2015 to 2019
$2.0M
NCI NIH HHS R01 CA184476
6 · The paper itself

Abstract

Integrative analysis based on quantitative representation of whole slide images (WSIs) in a large histology cohort may provide predictive models of clinical outcome. On one hand, the efficiency and effectiveness of such representation is hindered as a result of large technical variations (e.g., fixation, staining) and biological heterogeneities (e.g., cell type, cell state) that are always present in a large cohort. On the other hand, perceptual interpretation/validation of important multivariate phenotypic signatures are often difficult due to the loss of visual information during feature transformation in hyperspace. To address these issues, we propose a novel approach for integrative analysis based on cellular morphometric context, which is a robust representation of WSI, with the emphasis on tumor architecture and tumor heterogeneity, built upon cellular level morphometric features within the spatial pyramid matching (SPM) framework. The proposed approach is applied to The Cancer Genome Atlas (TCGA) lower grade glioma (LGG) cohort, where experimental results (i) reveal several clinically relevant cellular morphometric types, which enables both perceptual interpretation/validation and further investigation through gene set enrichment analysis; and (ii) indicate the significantly increased survival rates in one of the cellular morphometric context subtypes derived from the cellular morphometric context.

Indexed as

cellular morphometric contextcellular morphometric typeconsensus clusteringgene set enrichment analysislower grade gliomaspatial pyramid matchingsurvival analysis

Identifiers

PMID28018994
PMCPMC5181644
OpenAlexW2527477825

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.