Generates/modifies RNA-seq data for use in simulations. We provide a suite of functions that will add a known amount of signal to a real RNA-seq dataset. The advantage of using this approach over simulating under a theoretical distribution is that common/annoying aspects of the data are more preserved, giving a more realistic evaluation of your method. The main functions are select_counts(), thin_diff(), thin_lib(), thin_gene(), thin_2group(), thin_all(), and effective_cor(). See Gerard (2020) <doi:10.1186/s12859-020-3450-9> for details on the implemented methods.
Package details |
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| Author | David Gerard [aut, cre] (<https://orcid.org/0000-0001-9450-5023>) |
| Maintainer | David Gerard <gerard.1787@gmail.com> |
| License | GPL-3 |
| Version | 1.2.4 |
| URL | https://github.com/dcgerard/seqgendiff |
| Package repository | View on CRAN |
| Installation |
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