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PopPAnTe: population and pedigree association testing for quantitative data.
Visconti, Alessia; Al-Shafai, Mashael; Al Muftah, Wadha A; Zaghlool, Shaza B; Mangino, Massimo; Suhre, Karsten; Falchi, Mario.
Afiliação
  • Visconti A; Department of Twin Research and Genetic Epidemiology, King's College London, London, UK. alessia.visconti@kcl.ac.uk.
  • Al-Shafai M; Department of Genomics of Common Diseases, Imperial College London, London, UK.
  • Al Muftah WA; Department of Physiology and Biophysics, Weill Cornell Medical College in Qatar, Doha, Qatar.
  • Zaghlool SB; Research Division, Qatar Science Leadership Program, Qatar Foundation, Doha, Qatar.
  • Mangino M; Department of Biomedical Sciences, College of Health Sciences at Qatar University, Doha, Qatar.
  • Suhre K; Department of Genomics of Common Diseases, Imperial College London, London, UK.
  • Falchi M; Department of Physiology and Biophysics, Weill Cornell Medical College in Qatar, Doha, Qatar.
BMC Genomics ; 18(1): 150, 2017 02 10.
Article em En | MEDLINE | ID: mdl-28187711
ABSTRACT

BACKGROUND:

Family-based designs, from twin studies to isolated populations with their complex genealogical data, are a valuable resource for genetic studies of heritable molecular biomarkers. Existing software for family-based studies have mainly focused on facilitating association between response phenotypes and genetic markers, and no user-friendly tools are at present available to straightforwardly extend association studies in related samples to large datasets of generic quantitative data, as those generated by current -omics technologies.

RESULTS:

We developed PopPAnTe, a user-friendly Java program, which evaluates the association of quantitative data in related samples. Additionally, PopPAnTe implements data pre and post processing, region based testing, and empirical assessment of associations.

CONCLUSIONS:

PopPAnTe is an integrated and flexible framework for pairwise association testing in related samples with a large number of predictors and response variables. It works either with family data of any size and complexity, or, when the genealogical information is unknown, it uses genetic similarity information between individuals as those inferred from genome-wide genetic data. It can therefore be particularly useful in facilitating usage of biobank data collections from population isolates when extensive genealogical information is missing.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Linhagem / Software / Genômica Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male Idioma: En Revista: BMC Genomics Assunto da revista: GENETICA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Linhagem / Software / Genômica Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male Idioma: En Revista: BMC Genomics Assunto da revista: GENETICA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Reino Unido