| .tm_match | R Documentation |
Names first, then position. On a BSgenome the chr prefix is added
or removed as the genome requires, since that is a naming convention
rather than information; FASTA records and seqnames are matched
exactly, because theirs are arbitrary and guessing could match the wrong
one.
.tm_match(x, available, src)
x |
Identifiers to resolve. |
available |
The source's names, possibly empty strings. |
src |
The source, used for its kind and for error messages. |
Integer positions into available.
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