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denovolyzeR

Statistical Analyses of De Novo Genetic Variants

An integrated toolset for the analysis of de novo (sporadic) genetic sequence variants. denovolyzeR implements a mutational model that estimates the probability of a de novo genetic variant arising in each human gene, from which one can infer the expected number of de novo variants in a given population size. Observed variant frequencies can then be compared against expectation in a Poisson framework. denovolyzeR provides a suite of functions to implement these analyses for the interpretation of de novo variation in human disease.

Versions across snapshots

VersionRepositoryFileSize
0.2.0 rolling linux/jammy R-4.5 denovolyzeR_0.2.0.tar.gz 1.3 MiB
0.2.0 rolling linux/noble R-4.5 denovolyzeR_0.2.0.tar.gz 1.3 MiB
0.2.0 rolling source/ R- denovolyzeR_0.2.0.tar.gz 2.3 MiB
0.2.0 latest linux/jammy R-4.5 denovolyzeR_0.2.0.tar.gz 1.3 MiB
0.2.0 latest linux/noble R-4.5 denovolyzeR_0.2.0.tar.gz 1.3 MiB
0.2.0 latest source/ R- denovolyzeR_0.2.0.tar.gz 2.3 MiB
0.2.0 2026-04-26 source/ R- denovolyzeR_0.2.0.tar.gz 2.3 MiB
0.2.0 2026-04-23 source/ R- denovolyzeR_0.2.0.tar.gz 2.3 MiB
0.2.0 2026-04-09 windows/windows R-4.5 denovolyzeR_0.2.0.zip 1.3 MiB
0.2.0 2025-04-20 source/ R- denovolyzeR_0.2.0.tar.gz 2.3 MiB

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