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Focused goodness of fit tests for gene set analyses.
Zhang, Mengqi; Gelfman, Sahar; Martins Moreno, Cristiane Araujo; McCarthy, Janice M; Harms, Matthew B; Goldstein, David B; Allen, Andrew S.
Afiliación
  • Zhang M; Department of Biostatistics and Bioinformatics, Duke University, Durham,27710, North Carolina, USA.
  • Gelfman S; Center for Genomic and Computational Biology, Duke University, Durham,27710, North Carolina, USA.
  • Martins Moreno CA; Center for Statistical Genetics and Genomics, Duke University, Durham,27710, North Carolina, USA.
  • McCarthy JM; Institute of Genomic Medicine, Columbia University, New York City, 10032, New York, USA.
  • Harms MB; Institute of Genomic Medicine, Columbia University, New York City, 10032, New York, USA.
  • Goldstein DB; Department of Biostatistics and Bioinformatics, Duke University, Durham,27710, North Carolina, USA.
  • Allen AS; Institute of Genomic Medicine, Columbia University, New York City, 10032, New York, USA.
Brief Bioinform ; 23(1)2022 01 17.
Article en En | MEDLINE | ID: mdl-34849577
ABSTRACT
Gene set-based signal detection analyses are used to detect an association between a trait and a set of genes by accumulating signals across the genes in the gene set. Since signal detection is concerned with identifying whether any of the genes in the gene set are non-null, a goodness-of-fit (GOF) test can be used to compare whether the observed distribution of gene-level tests within the gene set agrees with the theoretical null distribution. Here, we present a flexible gene set-based signal detection framework based on tail-focused GOF statistics. We show that the power of the various statistics in this framework depends critically on two parameters the proportion of genes within the gene set that are non-null and the degree of separation between the null and alternative distributions of the gene-level tests. We give guidance on which statistic to choose for a given situation and implement the methods in a fast and user-friendly R package, wHC (https//github.com/mqzhanglab/wHC). Finally, we apply these methods to a whole exome sequencing study of amyotrophic lateral sclerosis.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Esclerosis Amiotrófica Lateral Límite: Humans Idioma: En Revista: Brief Bioinform Asunto de la revista: BIOLOGIA / INFORMATICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Esclerosis Amiotrófica Lateral Límite: Humans Idioma: En Revista: Brief Bioinform Asunto de la revista: BIOLOGIA / INFORMATICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos