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: | 1.3 |
| Depends: | CompQuadForm, dplyr, mgcv |
| Published: | 2020-08-06 |
| Author: | Amanda Brucker, Shannon T. Holloway, Jung-Ying Tzeng |
| Maintainer: | Shannon T. Holloway <sthollow at ncsu.edu> |
| License: | GPL-2 |
| NeedsCompilation: | no |
| CRAN checks: | CONCUR results |
| Reference manual: | CONCUR.pdf |
| Package source: | CONCUR_1.3.tar.gz |
| Windows binaries: | r-devel: CONCUR_1.2.zip, r-release: CONCUR_1.2.zip, r-oldrel: CONCUR_1.2.zip |
| macOS binaries: | r-release: CONCUR_1.2.tgz, r-oldrel: CONCUR_1.2.tgz |
| Old sources: | CONCUR archive |
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