Evidence map›Paper›PMID 33527996›Full record

ArticleBiostatistics (Oxford, England)2022

Estimation of the generation interval using pairwise relative transmission probabilities.

Sarah V Leavitt, Helen E Jenkins, Paola Sebastiani, Robyn S Lee, C Robert Horsburgh, Andrew M Tibbs, Laura F White

Abstract read
In one paragraph

Article in Biostatistics (Oxford, England), 2022. 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. 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

7 authors.

Sarah V LeavittDepartment of Biostatistics, Boston University School of Public Health, 801 Massachusetts Ave, Boston, MA 02118; Epidemiology Division, University of Toronto Dalla Lana School of Public Health, 155 College St Room 500, Toronto, ON M5T 3M7, Canada; Department of Epidemiology, Boston University School of Public Health, 801 Massachusetts Ave, Boston, MA 02118; and Massachusetts Department of Public Health, 250 Washington St, Boston, MA 02108.
Helen E JenkinsDepartment of Biostatistics, Boston University School of Public Health, 801 Massachusetts Ave, Boston, MA 02118; Epidemiology Division, University of Toronto Dalla Lana School of Public Health, 155 College St Room 500, Toronto, ON M5T 3M7, Canada; Department of Epidemiology, Boston University School of Public Health, 801 Massachusetts Ave, Boston, MA 02118; and Massachusetts Department of Public Health, 250 Washington St, Boston, MA 02108.
Paola SebastianiDepartment of Biostatistics, Boston University School of Public Health, 801 Massachusetts Ave, Boston, MA 02118; Epidemiology Division, University of Toronto Dalla Lana School of Public Health, 155 College St Room 500, Toronto, ON M5T 3M7, Canada; Department of Epidemiology, Boston University School of Public Health, 801 Massachusetts Ave, Boston, MA 02118; and Massachusetts Department of Public Health, 250 Washington St, Boston, MA 02108.
Robyn S LeeDepartment of Biostatistics, Boston University School of Public Health, 801 Massachusetts Ave, Boston, MA 02118; Epidemiology Division, University of Toronto Dalla Lana School of Public Health, 155 College St Room 500, Toronto, ON M5T 3M7, Canada; Department of Epidemiology, Boston University School of Public Health, 801 Massachusetts Ave, Boston, MA 02118; and Massachusetts Department of Public Health, 250 Washington St, Boston, MA 02108.
C Robert HorsburghDepartment of Biostatistics, Boston University School of Public Health, 801 Massachusetts Ave, Boston, MA 02118; Epidemiology Division, University of Toronto Dalla Lana School of Public Health, 155 College St Room 500, Toronto, ON M5T 3M7, Canada; Department of Epidemiology, Boston University School of Public Health, 801 Massachusetts Ave, Boston, MA 02118; and Massachusetts Department of Public Health, 250 Washington St, Boston, MA 02108.
Andrew M TibbsDepartment of Biostatistics, Boston University School of Public Health, 801 Massachusetts Ave, Boston, MA 02118; Epidemiology Division, University of Toronto Dalla Lana School of Public Health, 155 College St Room 500, Toronto, ON M5T 3M7, Canada; Department of Epidemiology, Boston University School of Public Health, 801 Massachusetts Ave, Boston, MA 02118; and Massachusetts Department of Public Health, 250 Washington St, Boston, MA 02108.
Laura F WhiteDepartment of Biostatistics, Boston University School of Public Health, 801 Massachusetts Ave, Boston, MA 02118; Epidemiology Division, University of Toronto Dalla Lana School of Public Health, 155 College St Room 500, Toronto, ON M5T 3M7, Canada; Department of Epidemiology, Boston University School of Public Health, 801 Massachusetts Ave, Boston, MA 02118; and Massachusetts Department of Public Health, 250 Washington St, Boston, MA 02108.

Funding

Translational ScienceP30AI042853 · NIAID · MIRIAM HOSPITAL · PI LARRY K BROWN · 1998 to 2026
$51.7M
Interdisciplinary Training for BiostatisticiansT32GM074905 · NIGMS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI WHITE, LAURA FORSBERG · 2005 to 2019
$3.0M
Supplement to Methods to Estimate the Effect of Interventions on the Incidence and Transmission of TuberculosisR01GM122876 · NIGMS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI WHITE, LAURA FORSBERG · 2017 to 2021
$1.9M
Maximizing Investigators' Research Award (R35)R35GM141821 · NIGMS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI WHITE, LAURA FORSBERG · 2021 to 2025
$1.8M
Understanding spatial heterogeneity of drug resistant tuberculosisK01AI102944 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI JENKINS, HELEN E. · 2013 to 2017
$627k
NIAID NIH HHS K01 AI102944NIAID NIH HHS P30 AI042853NIGMS NIH HHS R01 GM122876NIGMS NIH HHS R35 GM141821NIGMS NIH HHS T32 GM074905
6 · The paper itself

Abstract

The generation interval (the time between infection of primary and secondary cases) and its often used proxy, the serial interval (the time between symptom onset of primary and secondary cases) are critical parameters in understanding infectious disease dynamics. Because it is difficult to determine who infected whom, these important outbreak characteristics are not well understood for many diseases. We present a novel method for estimating transmission intervals using surveillance or outbreak investigation data that, unlike existing methods, does not require a contact tracing data or pathogen whole genome sequence data on all cases. We start with an expectation maximization algorithm and incorporate relative transmission probabilities with noise reduction. We use simulations to show that our method can accurately estimate the generation interval distribution for diseases with different reproductive numbers, generation intervals, and mutation rates. We then apply our method to routinely collected surveillance data from Massachusetts (2010-2016) to estimate the serial interval of tuberculosis in this setting.

Indexed as

Contact TracingTuberculosisDisease OutbreaksHumansProbabilityHierarchical clusteringKernel density estimationNoise reductionReproductive numberSerial intervalTuberculosis

Identifiers

PMID33527996
PMCPMC9291635

What OpenQuestion holds

Textmetadata
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.