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Implements a kernel-based association test for copy number variation (CNV) aggregate analysis in a certain genomic region (e.g., gene set, chromosome, or genome) that is robust to the within-locus and across-locus etiological heterogeneity, and bypass the need to define a "locus" unit for CNVs. Brucker, A., et al. (2020) <doi:10.1101/666875>.
| Version: | 1.4 |
| Depends: | CompQuadForm, dplyr, mgcv |
| Published: | 2022-06-07 |
| DOI: | 10.32614/CRAN.package.CONCUR |
| Author: | Amanda Brucker, Shannon T. Holloway, Jung-Ying Tzeng |
| Maintainer: | Shannon T. Holloway <shannon.t.holloway at gmail.com> |
| License: | GPL-2 |
| NeedsCompilation: | no |
| CRAN checks: | CONCUR results |
| Reference manual: | CONCUR.pdf |
| Package source: | CONCUR_1.4.tar.gz |
| Windows binaries: | r-devel: CONCUR_1.4.zip, r-release: CONCUR_1.4.zip, r-oldrel: CONCUR_1.4.zip |
| macOS binaries: | r-release (arm64): CONCUR_1.4.tgz, r-oldrel (arm64): CONCUR_1.4.tgz, r-release (x86_64): CONCUR_1.4.tgz, r-oldrel (x86_64): CONCUR_1.4.tgz |
| Old sources: | CONCUR archive |
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These binaries (installable software) and packages are in development.
They may not be fully stable and should be used with caution. We make no claims about them.