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Statistics to prioritize rare variants in family-based sequencing studies with disease subtypes

Authors: Nieuwoudt, Christina; Binte Farooq, Fabiha; Brooks-Wilson, Angela; Bureau, Alexandre; Graham, Jinko;

Statistics to prioritize rare variants in family-based sequencing studies with disease subtypes

Abstract

Code and Data for Analyses in Nieuwoudt et al. This repository contains the code and data for the analyses that appear in the preprint Statistics to prioritize rare variants in family-based sequencing studies with disease subtypes by Christina Nieuwoudt, Fabiha Binte Farooq, Angela Brooks-Wilson, Alexandre Bureau and Jinko Graham. The preprint can be found at the DOI https://doi.org/10.1101/2023.09.28.560053. Directory structure The files for the example data analysis from Section 3.1 of the preprint are in the directory Example of this repository. The files for the rank-only analysis in Appendix A of the preprint are in the directory RankOnly of this repository. See the README files in the respective directories for further details. R packages We do our analyses in R, and require the R packages SimRVSequences and RVMethods, available from GitHub. The package versions used in the analyses are archived at https://github.com/simrvprojects/SimRVSequences/releases/tag/v0.1 and https://github.com/simrvprojects/RVMethods/releases/tag/v0.1, respectively. Instructions for installing these packages are given in the Example/example.Rmd and RankOnly/rankonly.Rmd R Markdown files. Version numbers of other R packages installed as dependencies are shown in the following sessionInfo() output: attached base packages: [1] stats graphics grDevices utils datasets methods base other attached packages: [1] RVMethods_0.1.0 gRain_1.3.14 gRbase_1.9.0 [4] SimRVSequences_0.2.4 loaded via a namespace (and not attached): [1] Matrix_1.5-4 dplyr_1.1.3 compiler_4.3.0 [4] BiocManager_1.30.22 tidyselect_1.2.0 Rcpp_1.0.11 [7] stringr_1.5.0 tidyr_1.3.0 Rgraphviz_2.43.0 [10] lattice_0.21-8 SimRVPedigree_0.4.4 R6_2.5.1 [13] plyr_1.8.8 intervals_0.15.3 generics_0.1.3 [16] igraph_1.5.1 RBGL_1.75.0 knitr_1.43 [19] backports_1.4.1 BiocGenerics_0.45.3 graph_1.77.2 [22] tibble_3.2.1 pillar_1.9.0 rlang_1.1.1 [25] utf8_1.2.3 broom_1.0.5 stringi_1.7.12 [28] xfun_0.40 quadprog_1.5-8 cli_3.6.1 [31] magrittr_2.0.3 grid_4.3.0 kinship2_1.9.6 [34] lifecycle_1.0.3 vctrs_0.6.3 glue_1.6.2 [37] stats4_4.3.0 fansi_1.0.4 reshape2_1.4.4 [40] purrr_1.0.2 tools_4.3.0 pkgconfig_2.0.3 Funding acknowledgement • Natural Sciences and Engineering Research Council of Canada RGPIN-04296-2018 • Canadian Statistical Sciences Institute (CANSSI) Collaborative Research Team Project # 08 • Canadian Institutes for Health Research MOP-130311

Funding acknowledgement • Natural Sciences and Engineering Research Council of Canada RGPIN-04296-2018 • Canadian Statistical Sciences Institute (CANSSI) Collaborative Research Team Project # 08 • Canadian Institutes for Health Research MOP-130311

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Keywords

likelihood ratio, disease subtypes,, rare variant prioritization, exact tests, affected-only family design, family-based sequencing study, heritability

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popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
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This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
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