Evidence map›Paper›PMID 36929931›Full record

ArticleBioinformatics (Oxford, England)2023

GENLIB: new function to simulate haplotype transmission in large complex genealogies.

Mohan Rakesh, Hélène Vézina, Catherine Laprise, Ellen E Freeman, Kelly M Burkett, Marie-Hélène Roy-Gagnon

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Article in Bioinformatics (Oxford, England), 2023. 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

6 authors.

Mohan RakeshSchool of Epidemiology and Public Health, University of Ottawa, Ottawa, Ontario, Canada.
Hélène VézinaProjet BALSAC, Université du Québec à Chicoutimi, Chicoutimi, Québec, Canada.
Catherine LapriseCentre intersectoriel en santé durable, Université du Québec à Chicoutimi, Chicoutimi, Québec, Canada.
Ellen E FreemanSchool of Epidemiology and Public Health, University of Ottawa, Ottawa, Ontario, Canada.
Kelly M BurkettDepartment of Mathematics and Statistics, University of Ottawa, Ottawa, Ontario, Canada.
Marie-Hélène Roy-GagnonSchool of Epidemiology and Public Health, University of Ottawa, Ottawa, Ontario, Canada.ORCID 0000-0001-8747-0846

Funding

CIHR MOP 133560
6 · The paper itself

Abstract

summaryFounder populations with deep genealogical data are well suited for investigating genetic variants contributing to diseases. Here, we present a major update of the genealogical analysis R package GENLIB, centered around a new function which can simulate the transmission of haplotypes from founders to probands along very large and complex user-specified genealogies. AVAILABILITY AND IMPLEMENTATION: The latest update of the GENLIB package (v1.1.9) contains the new gen.simuHaplo() function and is available on the CRAN repository and from https://github.com/R-GENLIB/GENLIB. Examples can be accessed at https://github.com/R-GENLIB/simuhaplo_functions.

Indexed as

Population GroupsSoftwareHaplotypesHumans

Identifiers

PMID36929931
PMCPMC10049784

What OpenQuestion holds

Textfull text, public
LicenceCC BY
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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.