Evidence map›Paper›PMID 31054503›Full record

ArticleComputers in biology and medicine2019

Sensitivity analysis in digital pathology: Handling large number of parameters with compute expensive workflows.

Jeremias Gomes, Willian Barreiros, Tahsin Kurc, Alba C M A Melo, Jun Kong, Joel H Saltz, George Teodoro

Abstract read
In one paragraph

Article in Computers in biology and medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Jeremias GomesDepartment of Computer Science, University of Brasília, Brazil.
Willian BarreirosDepartment of Computer Science, University of Brasília, Brazil.
Tahsin KurcBiomedical Informatics Department, Stony Brook University, Stony Brook, USA; Scientific Data Group, Oak Ridge National Laboratory, Oak Ridge, USA.
Alba C M A MeloDepartment of Computer Science, University of Brasília, Brazil.
Jun KongBiomedical Informatics Department, Emory University, Atlanta, USA; Department of Biomedical Engineering, Emory-Georgia Institute of Technology, Atlanta, USA; Department of Mathematics and Statistics, Georgia State University, Atlanta, USA.
Joel H SaltzBiomedical Informatics Department, Stony Brook University, Stony Brook, USA.
George TeodoroDepartment of Computer Science, University of Brasília, Brazil; Biomedical Informatics Department, Stony Brook University, Stony Brook, USA. Electronic address: teodoro@unb.br.

Funding

TCIA Sustainment and Scalability - Platforms for Quantitative Imaging Informatics in Precision MedicineU24CA215109 · NCI · UNIV OF ARKANSAS FOR MED SCIS · PI BANERJEE, IMON, PRIOR, FRED WILLIAM · 2017 to 2021
$8.5M
Image Mining for Comparative Analysis of Expression Patterns in Tissue MicroarrayR01LM009239 · NLM · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI FORAN, DAVID J, SALTZ, JOEL H. · 2007 to 2016
$4.5M
Tools to Analyze Morphology and Spatially Mapped Molecular DataU24CA180924 · NCI · STATE UNIVERSITY NEW YORK STONY BROOK · PI SALTZ, JOEL H. · 2014 to 2019
$3.6M
Informatics for Integrative Brain Tumor Whole Slide AnalysisR01LM011119 · NLM · STATE UNIVERSITY NEW YORK STONY BROOK · PI FORAN, DAVID J, SALTZ, JOEL H. · 2011 to 2014
$1.8M
Methods and Tools for Integrating Pathomics Data into Cancer RegistriesUG3CA225021 · NCI · STATE UNIVERSITY NEW YORK STONY BROOK · PI DURBIN, ERIC B., FORAN, DAVID J · 2018 to 2019
$815k
Quantitative Analysis of GBM Invasion Mechanisms with New Imaging ProtocolK25CA181503 · NCI · GEORGIA STATE UNIVERSITY · PI KONG, JUN · 2014 to 2018
$592k
NCI NIH HHS K25 CA181503NCI NIH HHS U24 CA180924NCI NIH HHS U24 CA215109NCI NIH HHS UG3 CA225021NLM NIH HHS R01 LM009239NLM NIH HHS R01 LM011119
6 · The paper itself

Abstract

Digital pathology imaging enables valuable quantitative characterizations of tissue state at the sub-cellular level. While there is a growing set of methods for analysis of whole slide tissue images, many of them are sensitive to changes in input parameters. Evaluating how analysis results are affected by variations in input parameters is important for the development of robust methods. Executing algorithm sensitivity analyses by systematically varying input parameters is an expensive task because a single evaluation run with a moderate number of tissue images may take hours or days. Our work investigates the use of Surrogate Models (SMs) along with parallel execution to speed up parameter sensitivity analysis (SA). This approach significantly reduces the SA cost, because the SM execution is inexpensive. The evaluation of several SM strategies with two image segmentation workflows demonstrates that a SA study with SMs attains results close to a SA with real application runs (mean absolute error lower than 0.022), while the SM accelerates the SA execution by 51 × . We also show that, although the number of parameters in the example workflows is high, most of the uncertainty can be associated with a few parameters. In order to identify the impact of variations in segmentation results to downstream analyses, we carried out a survival analysis with 387 Lung Squamous Cell Carcinoma cases. This analysis was repeated using 3 values for the most significant parameters identified by the SA for the two segmentation algorithms; about 600 million cell nuclei were segmented per run. The results show that significance of the survival correlations of patient groups, assessed by a logrank test, are strongly affected by the segmentation parameter changes. This indicates that sensitivity analysis is an important tool for evaluating the stability of conclusions from image analyses.

Indexed as

AlgorithmsCarcinoma, Squamous CellImage Processing, Computer-AssistedLung NeoplasmsPattern Recognition, AutomatedWorkflowCell NucleusDatabases, FactualFemaleHumansMaleMicroscopySensitivity analysisSurrogate modelsSurvival analysisUncertainty propagationWhole Slide Image Analysis

Identifiers

PMID31054503
PMCPMC7363453

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.