query_genespace | R Documentation |
query_genespace
Functions to pull data stored in the /pangenome
and /syntenicHits directories
query_hits
extract syntenic (or all) hits that fall within a interval
in a genome.
query_pangenes
the primary engine to explore genespace output, this
lets you reformat the pan-genes to wide (entry - by - genome) matrix and
only look at specified positional bounds.
query_cnv
the primary engine to explore genespace output, this
lets you reformat the pan-genes to wide (entry - by - genome) matrix and
only look at specified positional bounds.
query_hits(gsParam, bed, synOnly = TRUE)
query_pangenes(
gsParam,
bed = NULL,
refGenome = NULL,
transform = TRUE,
showArrayMem = TRUE,
showNSOrtho = TRUE,
maxMem2Show = Inf,
showUnPlacedPgs = FALSE
)
query_cnv(gsParam, bed = NULL, onlyArrayReps = FALSE, maxCopyNumber = Inf)
gsParam |
A list of genespace parameters created by init_genespace. |
bed |
A data.table similar to the format of a bed file. At least two columns must be specified: genome, chr. These must match genome-chromosome combinations in the data. The user can also supply two additional columns: start, end. These are the base-pair start and end coordinates of each region. If start and end are not specified, they are set to 0 and Inf respectively so that the entire chromosome is returned. |
synOnly |
logical, given to query hits to return (or not) the synteny- constrained hits only |
refGenome |
character matching one of the genomeIDs if a bed object is not provided |
transform |
logical, should the pangenome be transformed from the long to the wide format? |
showArrayMem |
logical, should all genes or only the array representative genes (if FALSE) be shown? |
showNSOrtho |
logical, should non-syntenic orthologs be included in the output? |
maxMem2Show |
integer specifying the maximum number of members to be included in each entry-by-flag-by-genome combination. |
showUnPlacedPgs |
logical, when queried should un-located orthogroups be shown? |
onlyArrayReps |
logical, should only array representatives be considered for CNV counts? |
maxCopyNumber |
numeric, maximum copyNumber to tabulate. Orthogroups with more than this number are combined into the largest CNV category |
a list of data.tables named $genome, $chr: $start-$end. One data.table for each line in the bed file.
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