C Victor Jongeneel
Overview
Explore the profile of C Victor Jongeneel including associated specialties, affiliations and a list of published articles.
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40
Citations
1658
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Recent Articles
1.
Jongeneel C, Kotze M, Bhaw-Luximon A, Fadlelmola F, Fakim Y, Hamdi Y, et al.
Front Genet
. 2022 May;
13:769919.
PMID: 35571023
Genomics policy development involves assessing a wide range of issues extending from specimen collection and data sharing to whether and how to utilize advanced technologies in clinical practice and public...
2.
Aron S, Jongeneel C, Chauke P, Chaouch M, Kumuthini J, Zass L, et al.
PLoS Comput Biol
. 2021 Dec;
17(12):e1009592.
PMID: 34882684
No abstract available.
3.
Ahmed A, Mpangase P, Panji S, Baichoo S, Souilmi Y, Fadlelmola F, et al.
AAS Open Res
. 2020 May;
1:9.
PMID: 32382696
The need for portable and reproducible genomics analysis pipelines is growing globally as well as in Africa, especially with the growth of collaborative projects like the Human Health and Heredity...
4.
Blatti 3rd C, Emad A, Berry M, Gatzke L, Epstein M, Lanier D, et al.
PLoS Biol
. 2020 Jan;
18(1):e3000583.
PMID: 31971940
We present Knowledge Engine for Genomics (KnowEnG), a free-to-use computational system for analysis of genomics data sets, designed to accelerate biomedical discovery. It includes tools for popular bioinformatics tasks such...
5.
Baichoo S, Souilmi Y, Panji S, Botha G, Meintjes A, Hazelhurst S, et al.
BMC Bioinformatics
. 2018 Nov;
19(1):457.
PMID: 30486782
Background: The Pan-African bioinformatics network, H3ABioNet, comprises 27 research institutions in 17 African countries. H3ABioNet is part of the Human Health and Heredity in Africa program (H3Africa), an African-led research...
6.
Jongeneel C, Achinike-Oduaran O, Adebiyi E, Adebiyi M, Adeyemi S, Akanle B, et al.
PLoS Comput Biol
. 2017 Jun;
13(6):e1005419.
PMID: 28570565
The H3ABioNet pan-African bioinformatics network, which is funded to support the Human Heredity and Health in Africa (H3Africa) program, has developed node-assessment exercises to gauge the ability of its participating...
7.
Mulder N, Adebiyi E, Alami R, BenKahla A, Brandful J, Doumbia S, et al.
Genome Res
. 2015 Dec;
26(2):271-7.
PMID: 26627985
The application of genomics technologies to medicine and biomedical research is increasing in popularity, made possible by new high-throughput genotyping and sequencing technologies and improved data analysis capabilities. Some of...
8.
Valsesia A, Stevenson B, Waterworth D, Mooser V, Vollenweider P, Waeber G, et al.
BMC Genomics
. 2012 Jun;
13:241.
PMID: 22702538
Background: Genotypes obtained with commercial SNP arrays have been extensively used in many large case-control or population-based cohorts for SNP-based genome-wide association studies for a multitude of traits. Yet, these...
9.
Nikolaev S, Rimoldi D, Iseli C, Valsesia A, Robyr D, Gehrig C, et al.
Nat Genet
. 2011 Dec;
44(2):133-9.
PMID: 22197931
We performed exome sequencing to detect somatic mutations in protein-coding regions in seven melanoma cell lines and donor-matched germline cells. All melanoma samples had high numbers of somatic mutations, which...
10.
Valsesia A, Rimoldi D, Martinet D, Ibberson M, Benaglio P, Quadroni M, et al.
PLoS One
. 2011 Apr;
6(4):e18369.
PMID: 21494657
Cancer genomes frequently contain somatic copy number alterations (SCNA) that can significantly perturb the expression level of affected genes and thus disrupt pathways controlling normal growth. In melanoma, many studies...