A bioinformatics pipeline for rare genetic diseases in South African patients

The research fields of bioinformatics and computational biology are growing rapidly in South Africa. Bioinformatics pipelines play an integral part in handling sequencing data, which are used to investigate the aetiology of common and rare diseases. Bioinformatics platforms for common disease aetiol...

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Main Authors: Maryke Schoonen, Albertus S. Seyffert, Francois H. van der Westhuizen, Izelle Smuts
Format: Article
Language:English
Published: Academy of Science of South Africa 2019-03-01
Series:South African Journal of Science
Subjects:
Online Access:https://www.sajs.co.za/article/view/4876
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spelling doaj-6851da80528343c48288165a10fe8dde2020-11-25T01:55:52ZengAcademy of Science of South AfricaSouth African Journal of Science1996-74892019-03-011153/410.17159/sajs.2019/48764876A bioinformatics pipeline for rare genetic diseases in South African patientsMaryke Schoonen0Albertus S. Seyffert1Francois H. van der Westhuizen2Izelle Smuts3Human Metabolomics, North-West University, Potchefstroom, South AfricaCentre for Space Research, North-West University, Potchefstroom, South AfricaHuman Metabolomics, North-West University, Potchefstroom, South AfricaDepartment of Paediatrics and Child Health, Steve Biko Academic Hospital, University of Pretoria, Pretoria, South AfricaThe research fields of bioinformatics and computational biology are growing rapidly in South Africa. Bioinformatics pipelines play an integral part in handling sequencing data, which are used to investigate the aetiology of common and rare diseases. Bioinformatics platforms for common disease aetiology are well supported and continuously being developed in South Africa. However, the same is not the case for rare diseases aetiology research. Investigations into the latter rely on international cloud-based tools for data analyses and ultimately confirmation of a genetic disease. However, these tools are not necessarily optimised for ethnically diverse population groups. We present an in-house developed bioinformatics pipeline to enable researchers to annotate and filter variants in either exome or amplicon next-generation sequencing data. This pipeline was developed using next-generation sequencing data of a predominantly African cohort of patients diagnosed with rare disease. Significance: • We demonstrate the feasibility of in-country development of ethnicity-sensitive, automated bioinformatics pipelines using free software in a South African context. • We provide a roadmap for development of similarly ethnicity-sensitive bioinformatics pipelines.https://www.sajs.co.za/article/view/4876computational toolsafrican cohortnext-generation sequencingrare disease
collection DOAJ
language English
format Article
sources DOAJ
author Maryke Schoonen
Albertus S. Seyffert
Francois H. van der Westhuizen
Izelle Smuts
spellingShingle Maryke Schoonen
Albertus S. Seyffert
Francois H. van der Westhuizen
Izelle Smuts
A bioinformatics pipeline for rare genetic diseases in South African patients
South African Journal of Science
computational tools
african cohort
next-generation sequencing
rare disease
author_facet Maryke Schoonen
Albertus S. Seyffert
Francois H. van der Westhuizen
Izelle Smuts
author_sort Maryke Schoonen
title A bioinformatics pipeline for rare genetic diseases in South African patients
title_short A bioinformatics pipeline for rare genetic diseases in South African patients
title_full A bioinformatics pipeline for rare genetic diseases in South African patients
title_fullStr A bioinformatics pipeline for rare genetic diseases in South African patients
title_full_unstemmed A bioinformatics pipeline for rare genetic diseases in South African patients
title_sort bioinformatics pipeline for rare genetic diseases in south african patients
publisher Academy of Science of South Africa
series South African Journal of Science
issn 1996-7489
publishDate 2019-03-01
description The research fields of bioinformatics and computational biology are growing rapidly in South Africa. Bioinformatics pipelines play an integral part in handling sequencing data, which are used to investigate the aetiology of common and rare diseases. Bioinformatics platforms for common disease aetiology are well supported and continuously being developed in South Africa. However, the same is not the case for rare diseases aetiology research. Investigations into the latter rely on international cloud-based tools for data analyses and ultimately confirmation of a genetic disease. However, these tools are not necessarily optimised for ethnically diverse population groups. We present an in-house developed bioinformatics pipeline to enable researchers to annotate and filter variants in either exome or amplicon next-generation sequencing data. This pipeline was developed using next-generation sequencing data of a predominantly African cohort of patients diagnosed with rare disease. Significance: • We demonstrate the feasibility of in-country development of ethnicity-sensitive, automated bioinformatics pipelines using free software in a South African context. • We provide a roadmap for development of similarly ethnicity-sensitive bioinformatics pipelines.
topic computational tools
african cohort
next-generation sequencing
rare disease
url https://www.sajs.co.za/article/view/4876
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