Evidence map›Paper›PMID 26306274›Full record

ArticleAMIA Joint Summits on Translational Science proceedings. AMIA Joint Summits on Translational Science2015

Conceptualizing a Novel Quasi-Continuous Bayesian Phylogeographic Framework for Spatiotemporal Hypothesis Testing.

Daniel Magee, Matthew Scotch

Abstract read
In one paragraph

Article in AMIA Joint Summits on Translational Science proceedings. AMIA Joint Summits on Translational Science, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

2 authors.

Daniel MageeArizona State University, Tempe, AZ, USA.
Matthew ScotchArizona State University, Tempe, AZ, USA.

Funding

Informatics for zoonotic disease surveillance: combining animal and human dataR00LM009825 · NLM · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI SCOTCH, MATTHEW · 2010 to 2012
$723k
NLM NIH HHS R00 LM009825
6 · The paper itself

Abstract

Continuous phylogeography is a growing approach to studying the spatiotemporal origins of RNA viruses because of its realistic spatial reconstruction advantages over discrete phylogeography. While the generalized linear model has been demonstrated as an effective tool for simultaneously assessing the drivers impacting viral diffusion in discrete phylogeography, there is no similar testing method in the continuous phylogeographic framework. In this paper, we take a step toward bridging that gap by conceptualizing a novel quasi-continuous approach which enables the addition of discrete locations beyond the known sampling locations of the virus. Our model, when fully developed into phylogeographic software, will enable spatiotemporal hypothesis testing of viral diffusion without being strictly limited to observed sampling locations. This model can still assess the impact of local epidemiological variables on virus spread and could provide public health agencies with more realistic estimates of key predictors and locations by utilizing a more continuous landscape.

Identifiers

PMID26306274
PMCPMC4525269

What OpenQuestion holds

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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.