Evidence map›Paper›PMID 28957497›Full record

ArticleBioinformatics (Oxford, England)2017

A multi-scenario genome-wide medical population genetics simulation framework.

Jacquiline W Mugo, Ephifania Geza, Joel Defo, Samar S M Elsheikh, Gaston K Mazandu, Nicola J Mulder, Emile R Chimusa

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2017. 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

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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
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4 · The record

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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.

Jacquiline W MugoDepartment of Integrative Biomedical Sciences, Computational Biology Division, Institute of Infectious Disease and Molecular Medicine, University of Cape Town, Medical School, Observatory, Cape Town 7925, South Africa.
Ephifania GezaDepartment of Integrative Biomedical Sciences, Computational Biology Division, Institute of Infectious Disease and Molecular Medicine, University of Cape Town, Medical School, Observatory, Cape Town 7925, South Africa.
Joel DefoDepartment of Integrative Biomedical Sciences, Computational Biology Division, Institute of Infectious Disease and Molecular Medicine, University of Cape Town, Medical School, Observatory, Cape Town 7925, South Africa.
Samar S M ElsheikhDepartment of Integrative Biomedical Sciences, Computational Biology Division, Institute of Infectious Disease and Molecular Medicine, University of Cape Town, Medical School, Observatory, Cape Town 7925, South Africa.
Gaston K MazanduDepartment of Integrative Biomedical Sciences, Computational Biology Division, Institute of Infectious Disease and Molecular Medicine, University of Cape Town, Medical School, Observatory, Cape Town 7925, South Africa.
Nicola J MulderDepartment of Integrative Biomedical Sciences, Computational Biology Division, Institute of Infectious Disease and Molecular Medicine, University of Cape Town, Medical School, Observatory, Cape Town 7925, South Africa.
Emile R ChimusaDepartment of Pathology, Division of Human Genetics, Faculty of Health Sciences, Institute of Infectious Disease and Molecular Medicine, University of Cape Town, Observatory, Cape Town 7925, South Africa.

Funding

H3ABioNet: a sustainable African Bioinformatics Network for H3AfricaU41HG006941 · NHGRI · UNIVERSITY OF CAPE TOWN · PI MULDER, NICOLA · 2012 to 2017
$14.8M
H3ABioNet: informatics solutions for H3AfricaU24HG006941 · NHGRI · UNIVERSITY OF CAPE TOWN · PI MULDER, NICOLA · 2017 to 2021
$12.9M
NHGRI NIH HHS U24 HG006941NHGRI NIH HHS U41 HG006941
6 · The paper itself

Abstract

motivationRecent technological advances in high-throughput sequencing and genotyping have facilitated an improved understanding of genomic structure and disease-associated genetic factors. In this context, simulation models can play a critical role in revealing various evolutionary and demographic effects on genomic variation, enabling researchers to assess existing and design novel analytical approaches. Although various simulation frameworks have been suggested, they do not account for natural selection in admixture processes. Most are tailored to a single chromosome or a genomic region, very few capture large-scale genomic data, and most are not accessible for genomic communities.

resultsHere we develop a multi-scenario genome-wide medical population genetics simulation framework called 'FractalSIM'. FractalSIM has the capability to accurately mimic and generate genome-wide data under various genetic models on genetic diversity, genomic variation affecting diseases and DNA sequence patterns of admixed and/or homogeneous populations. Moreover, the framework accounts for natural selection in both homogeneous and admixture processes. The outputs of FractalSIM have been assessed using popular tools, and the results demonstrated its capability to accurately mimic real scenarios. They can be used to evaluate the performance of a range of genomic tools from ancestry inference to genome-wide association studies. AVAILABILITY AND IMPLEMENTATION: The FractalSIM package is available at http://www.cbio.uct.ac.za/FractalSIM. CONTACT: emile.chimusa@uct.ac.za. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

Genetics, PopulationGenetic VariationGenomeGenome-Wide Association StudyGenomicsHigh-Throughput Nucleotide SequencingHumansPolymorphism, Single NucleotideSelection, GeneticSequence Analysis, DNASoftware

Identifiers

PMID28957497
PMCPMC5870573

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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.