Description Usage Arguments Value See Also Examples
In this package, big data frames are generated from cohort wide vcf-like
files. This function constructs a VRanges object from such a data frame by
using makeGRangesFromDataFrame
from the package
GenomicRanges
1 2 3 4 5 | makeVRangesFromDataFrame(in_df, in_keep.extra.columns = TRUE,
in_seqinfo = NULL, in_seqnames.field = "X.CHROM",
in_start.field = "POS", in_end.field = "POS", in_PID.field = "PID",
in_subgroup.field = "subgroup", in_strand.field = "strand",
verbose_flag = 1)
|
in_df |
A big dataframe constructed from a vcf-like file of a whole cohort. The first columns are those of a standard vcf file, followed by an arbitrary number of custom or user defined columns. One of these can carry a PID (patient or sample identifyier) and one can carry subgroup information. |
in_keep.extra.columns |
in_seqinfo
Argument passed on to |
in_seqinfo |
A seqInfo object, referring to the reference genome used.
Argument passed on to |
in_seqnames.field |
Indicates the name of the column in which the chromosome is encoded |
in_start.field |
Indicates the name of the column in which the start coordinate is encoded |
in_end.field |
Indicates the name of the column in which the end coordinate is encoded |
in_PID.field |
Indicates the name of the column in which the PID (patient or sample identifier) is encoded |
in_subgroup.field |
Indicates the name of the column in which the subgroup information is encoded |
in_strand.field |
Indicates the name of the column in which the strandedness is encoded |
verbose_flag |
Verbose if 1 |
The constructed VRanges object
1 2 3 4 5 | data(lymphoma_test)
temp_vr <- makeVRangesFromDataFrame(lymphoma_test_df,
in_seqnames.field="CHROM",
in_subgroup.field="SUBGROUP",
verbose_flag=1)
|
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.