prio | R Documentation |
This method allows to select strain combinations which best refine a specified genetic region (GRCm38). E.g. if a crossing experiment with two inbred mouse strains 'strain1' and 'strain2' resulted in a QTL, the outputted strain combinations can be used to refine the respective region in further crossing experiments.
prio(
chr,
start = NULL,
end = NULL,
strain1 = NULL,
strain2 = NULL,
consequence = NULL,
impact = NULL,
min_strain_benef = 0.1,
max_set_size = 3,
return_obj = "dataframe"
)
chr |
Vector of chromosome names. |
start |
Optional vector of chromosomal start positions of target regions (GRCm38). |
end |
Optional vector of chromosomal end positions of target regions (GRCm38). |
strain1 |
First strain set with strains from avail_strains(). |
strain2 |
Second strain set with strains from avail_strains(). |
consequence |
Optional vector of consequence types. |
impact |
Optional vector of impact types. |
min_strain_benef |
Minimum reduction factor (min) of a single strain. |
max_set_size |
Maximum set of strains. |
return_obj |
The user can choose to get the result to be returned as data frame ("dataframe") or as a GenomicRanges::GRanges ("granges") object. Default value is "data frame". |
Data frame
res = prio("chr1",
start = 5000000, end = 6000000, strain1 = "C57BL_6J",
strain2 = "AKR_J"
)
comment(res$genotypes)
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