View source: R/shiny_related_functions.R
VCFsToDBSCatalogs | R Documentation |
Create a list of 3 catalogs (one each for DBS78, DBS144 and DBS136) out of the contents in list.of.DBS.vcfs. The VCFs must not contain any type of mutation other then DBSs.
VCFsToDBSCatalogs(
list.of.DBS.vcfs,
ref.genome,
num.of.cores = 1,
trans.ranges = NULL,
region = "unknown",
return.annotated.vcfs = FALSE,
suppress.discarded.variants.warnings = TRUE
)
list.of.DBS.vcfs |
List of in-memory data frames of pure DBS mutations – no SBS or 3+BS mutations. The list names will be the sample ids in the output catalog. |
ref.genome |
A |
num.of.cores |
The number of cores to use. Not available on Windows
unless |
trans.ranges |
Optional. If
then the function will infer |
region |
A character string designating a genomic region;
see |
return.annotated.vcfs |
Logical. Whether to return the annotated VCFs with additional columns showing mutation class for each variant. Default is FALSE. |
suppress.discarded.variants.warnings |
Logical. Whether to suppress warning messages showing information about the discarded variants. Default is TRUE. |
A list containing the following objects:
catDBS78
, catDBS136
, catDBS144
: Matrix of
3 DBS catalogs (one each for 78, 136, and 144).
discarded.variants
: Non-NULL only if there are variants
that were excluded from the analysis. See the added extra column
discarded.reason
for more details.
annotated.vcfs
: Non-NULL only if
return.annotated.vcfs
= TRUE. DBS VCF annotated by
AnnotateDBSVCF
with three new columns DBS78.class
,
DBS136.class
and DBS144.class
showing the mutation class for
each DBS variant.
If trans.ranges
is not provided by user and cannot be inferred by
ICAMS, DBS 144 catalog will not be generated. Each catalog has
attributes added. See as.catalog
for more details.
To add or change attributes of the catalog, you can use function
attr
.
For example, attr(catalog, "abundance")
<- custom.abundance
.
DBS 144 catalog only contains mutations in transcribed regions.
file <- c(system.file("extdata/Mutect-vcf",
"Mutect.GRCh37.s1.vcf",
package = "ICAMS"))
list.of.DBS.vcfs <- ReadAndSplitMutectVCFs(file)$DBS
if (requireNamespace("BSgenome.Hsapiens.1000genomes.hs37d5", quietly = TRUE)) {
catalogs.DBS <- VCFsToDBSCatalogs(list.of.DBS.vcfs, ref.genome = "hg19",
trans.ranges = trans.ranges.GRCh37,
region = "genome")}
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