Evidence map›Paper›PMID 31135022›Full record

ArticleBioinformatics (Oxford, England)2019

Deep fusion of contextual and object-based representations for delineation of multiple nuclear phenotypes.

Mina Khoshdeli, Garrett Winkelmaier, Bahram Parvin

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. CD36International journal of molecular sciences · 2022
    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

3 authors.

Mina KhoshdeliDepartment of Electrical and Biomedical Engineering, University of Nevada, Reno, NV 89557-0260, USA.
Garrett WinkelmaierDepartment of Electrical and Biomedical Engineering, University of Nevada, Reno, NV 89557-0260, USA.
Bahram ParvinDepartment of Electrical and Biomedical Engineering, University of Nevada, Reno, NV 89557-0260, USA.

Funding

Stratifying brain tumors by structural subtyping and heterogeneityR15CA235430 · NCI · UNIVERSITY OF NEVADA RENO · PI PARVIN, BAHRAM A. · 2019 to 2019
$430k
NCI NIH HHS R15 CA235430
6 · The paper itself

Abstract

motivationNuclear delineation and phenotypic profiling are important steps in the automated analysis of histology sections. However, these are challenging problems due to (i) technical variations (e.g. fixation, staining) that originate as a result of sample preparation; (ii) biological heterogeneity (e.g. vesicular versus high chromatin phenotypes, nuclear atypia) and (iii) overlapping nuclei. This Application-Note couples contextual information about the cellular organization with the individual signature of nuclei to improve performance. As a result, routine delineation of nuclei in H&E stained histology sections is enabled for either computer-aided pathology or integration with genome-wide molecular data.

resultsThe method has been evaluated on two independent datasets. One dataset originates from our lab and includes H&E stained sections of brain and breast samples. The second dataset is publicly available through IEEE with a focus on gland-based tissue architecture. We report an approximate AJI of 0.592 and an F1-score 0.93 on both datasets. AVAILABILITY AND IMPLEMENTATION: The code-base, modified dataset and results are publicly available. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

Cell NucleusHistological TechniquesChromatinGenomePhenotypeChromatin

Identifiers

PMID31135022
PMCPMC6853689

What OpenQuestion holds

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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.