knitr::opts_chunk$set( collapse = TRUE, comment = "#>" )
This R package provides methods for genetic finemapping in inbred mice by taking advantage of their very high homozygosity rate (>95%).
For one ore more chromosomal regions (GRCm38), method finemap
extracts homozygous SNVs for which the allele differs between two sets of strains (e.g. case vs controls) and outputs respective causal SNV/gene candidates.
if(!requireNamespace("BiocManager", quietly = TRUE)) install.packages("BiocManager") BiocManager::install("MouseFM")
library(MouseFM)
Available mouse strains
avail_strains()
Call finemap to finemap a specific region
res = finemap(chr="chr7", strain1=c("C57BL_6J","C57L_J","CBA_J","NZB_B1NJ"), strain2=c("C3H_HEJ","MOLF_EiJ","NZW_LacJ","WSB_EiJ","SPRET_EiJ"), impact=c("HIGH", "MODERATE", "LOW")) res[1:10,]
View meta information
comment(res)
Annotate with consequences (Not recommended for large queries!)
cons = annotate_consequences(res, "mouse")
Annotate with genes
genes = annotate_mouse_genes(res, flanking = 50000)
The output of sessionInfo()
on the system
on which this document was compiled:
sessionInfo()
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