prepareOl | R Documentation |
Prepare SV overlaps before annotation
prepareOl(
query,
subject,
min.rol = 0.1,
max.ins.dist = 1,
range.seq.comp = FALSE,
ins.seq.comp = FALSE,
nb.cores = 1,
by.gt = FALSE
)
query |
a query GRanges object |
subject |
a subject GRanges object |
min.rol |
minimum reciprocal overlap for deletions and other "ranges" SVs. Default is 0.1 |
max.ins.dist |
maximum distance for insertions to be clustered. |
range.seq.comp |
compare sequence instead of overlapping deletions/inversion/etc. Default is FALSE. |
ins.seq.comp |
compare sequence instead of insertion sizes. Default is FALSE. |
nb.cores |
number of processors to use. Default is 1. |
by.gt |
should the variants be split by genotype? Default is FALSE, i.e. all variants with an alternate allele (ac>0) is considered 'called'. |
a GRanges with information about pairs of SVs in query and subject that overlap
GRange |
intersected ranges (for "ranges" SVs) |
queryHits |
the id of the input query |
subjectHits |
the id of the input subject |
querSize |
the size of the input query |
subjectSize |
the size of the input subject |
interSize |
the size of the intersection (e.g. range, ins size, ins seq alignment) |
type |
the SV type of the pair |
Jean Monlong
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