Description Usage Arguments Value
View source: R/guide_alignments.R
Read BAM file report, filter with valid PAM sequence, report # of alignments
1 2 3 | guideAlignments(bam.file, max.alns = 100, pam = "[ACGTN]GG|GG[ACGTN]",
genome_id = "hg19", chromosomes = paste0("chr", c(as.character(1:22), "X",
"Y")), include.no.align = F, as.df = T, guide_length = 20)
|
bam.file |
BAM file path |
max.alns |
only consider guides with fewer than this many alignments |
pam |
PAM sequence as regular expression |
include.no.align |
include guides that do not map to genome |
as.df |
return data.frame if |
data.frame or GRanges object of results
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