- lsn.data
Original input lesion data.
- gene.data
Original input gene annotation data.
- gene.lsn.data
A data.frame ordered by chromosome and start position, containing both gene and lesion entries.
Each row includes a cty code indicating the type and boundary of the interval:
1 = gene start, 2 = lesion start, 3 = lesion end, 4 = gene end.
- gene.lsn.hits
A data.frame where each row corresponds to a gene overlapped by a lesion.
Includes 11 columns:
"gene" (Ensembl gene ID),
"gene.chrom", "gene.loc.start", "gene.loc.end" (chromosome and coordinates of the gene),
"ID" (patient/sample ID),
"lsn.chrom", "lsn.loc.start", "lsn.loc.end" (chromosome and coordinates of the lesion),
and "lsn.type" (type of lesion).
- gene.index
A data.frame indexing the rows in gene.lsn.data that correspond to each chromosome's genes (row start and row end per chromosome).
- lsn.index
A data.frame indexing the rows in gene.lsn.data that correspond to each lesion (row start and row end per lesion).