INTERNAL: Map a genomic range to the alignment
1 | minimum(a, b)
|
cr |
cut range (the range within a genomic hit range which we want to slice from an alignment) |
map_min |
Minumum position in the genomic map. |
map_max |
Maximum position in the genomic map |
ghr |
genomic hit range (range of an orthologous genomic segment within a genome) |
ahr |
alignment hit range (degapped range of an orthologous genomic segment within a genome) |
gaps |
gapranges |
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