Evidence map›Paper›PMID 38032776›Full record

ArticleIEEE journal of biomedical and health informatics2024

Estimation of Circular Statistics in the Presence of Measurement Bias.

Abdallah Alsammani, William C Stacey, Stephen V Gliske

Abstract read
In one paragraph

Article in IEEE journal of biomedical and health informatics, 2024. 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

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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. Article
  2. 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.

Abdallah Alsammani
William C Stacey
Stephen V Gliske

Funding

Michigan Institute for Clinical and Health Research (MCHR)UL1TR000433 · NCATS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MASHOUR, GEORGE ALEXANDER · 2012 to 2016
$49.9M
Characterizing High Frequency Oscillations as an epilepsy biomarker with Big Data toolsR01NS094399 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI STACEY, WILLIAM CHARLES · 2015 to 2025
$4.1M
Modeling seizure precursors and antiepileptic brain stimulationK08NS069783 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI STACEY, WILLIAM CHARLES · 2011 to 2015
$886k
Epileptic biomarkers and big data: identifying brain regions to resect in patients with refractory epilepsyK01ES026839 · NIEHS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GLISKE, STEPHEN V · 2015 to 2019
$734k
Doris Duke Charitable Foundation 2015096NCATS NIH HHS UL1 TR000433NIEHS NIH HHS K01 ES026839NINDS NIH HHS K08 NS069783NINDS NIH HHS R01 NS094399
6 · The paper itself

Abstract

Circular statistics and Rayleigh tests are important tools for analyzing cyclic events. However, current methods are not robust to significant measurement bias, especially incomplete or otherwise non-uniform sampling. One example is studying 24-cyclicity but having data not recorded uniformly over the full 24-hour cycle. Our objective is to present a robust method to estimate circular statistics and their statistical significance in the presence of incomplete or otherwise non-uniform sampling. Our method is to solve the underlying Fredholm Integral Equation for the more general problem, estimating probability distributions in the context of imperfect measurements, with our circular statistics in the presence of incomplete/non-uniform sampling being one special case. The method is based on linear parameterizations of the underlying distributions. We simulated the estimation error of our approach for several toy examples as well as for a real-world example: analyzing the 24-hour cyclicity of an electrographic biomarker of epileptic tissue controlled for states of vigilance. We also evaluated the accuracy of the Rayleigh test statistic versus the direct simulation of statistical significance. Our method shows a very low estimation error. In the real-world example, the corrected moments had a root mean square error of [Formula: see text]. In contrast, the Rayleigh test statistic overestimated the statistical significance and was thus not reliable. The presented methods thus provide a robust solution to computing circular moments even with incomplete or otherwise non-uniform sampling. Since Rayleigh test statistics cannot be used in this circumstance, direct estimation of significance is the preferable option for estimating statistical significance.

Indexed as

Computer SimulationBiasHumansProbability

Identifiers

PMID38032776
PMCPMC10964323

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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.