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This method returns a dataframe representing the allelic fragmentation of each sampled cell.

Value

A dataframe reporting, for each cell, for each genomic fragment, and for all the allelic type on the genomic fragment, the cell identifier (cell_id), the chromosome (chr), the first base position (begin), the last base position (end), and the number of copy of the major and minor alleles (major and minor, respectively).

See also

vignette("mutations") for usage examples