Uses the results of locate_codons to determine whether there is an available PAM with desired spacing from the genomic coordinate of the targeted base.
1 2 3 4 5 6 7 8 | locate_PAM(
codons,
genome,
spacing = PAM_spacing(),
PAM = PAM_patterns_default(),
flanking = 150,
keep_PAM = FALSE
)
|
codons |
A dataframe resulting from locate_codons. |
genome |
A BSgenome sequence database,
or a Biostrings. Used to extract the genomic sequence context
for each genomic coordinate in |
spacing |
The result of PAM_spacing, which is a named list of two-element
numeric vectors. Each two-element vector defines a range of spacing between an
edited base and the PAM (i.e. the minimum and maximum allowable nucleotides between
the targeted base and the PAM). Each pair of ranges is checked in order with the
first range prioritized over the next. Defaults to |
PAM |
A named list of PAM patterns to be considered (see PAM_pattern). Names
correspond to resulting column names in the returned dataframe. Default PAM patterns
include |
flanking |
An number specifying how much flanking genomic context to return in the resulting dataframe. Defaults to 150. |
keep_PAM |
Logical. Should the PAM sequence be included in the guides?
Defaults to |
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