integrate_synteny | R Documentation |
integrate_synteny
Internal functions to connect syntenic positions for
riparian plotting and interpolated gene order calculation for placement of
syntenic pan-genes.
interp_synPos
pipes data to interp_approx and combines across genomes
phase_blks
splits blocks so that each is anchored to a single
reference genome chromosome, which allows the construction of default
riparian plots
nophase_blks
simple wrapper for calc_blkCoords so that block
coordinates are calculated across all combination of genomes.
calc_blkCoords
from a hits object, determine block coordinates,
orientation and membership
interp_synPos(gsParam, verbose = TRUE)
phase_blks(
gsParam,
refGenome,
useRegions,
blkSize = 5,
synBuff = 100,
refChr = NULL,
refStartBp = NULL,
refEndBp = NULL
)
nophase_blks(gsParam, useRegions, blkSize = 5)
calc_blkCoords(hits, mirror = FALSE)
gsParam |
A list of genespace parameters created by init_genespace. |
verbose |
logical, should updates be printed to the console? |
refGenome |
Character string specifying the reference genome to use |
useRegions |
Logical, should regions be used instead of blocks? |
blkSize |
see init_genesapce |
synBuff |
see init_genesapce |
refChr |
string matching chromosome IDs in refGenome |
refStartBp |
physical (bp) region start coordinate on refChr |
refEndBp |
physical (bp) region end coordinate on refChr |
hits |
data.table with hits (see read_synHits) |
mirror |
logical, should the block coordinates be mirrored between query and target genomes |
Functions here should not be called directly by the user except if customizing riparian plots.
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