The RaggedExperiment package provides a flexible data
representation for copy number, mutation and other ragged array schema for
genomic location data. The output of Allele-Specific Copy number Analysis of
Tumors (ASCAT) can be classed as a ragged array and contains whole genome
allele-specific copy number information for each sample in the analysis. For
more information on ASCAT and guidelines on how to generate ASCAT data please
see the ASCAT
website and
github. To carry out further analysis of
the ASCAT data, utilising the functionalities of RaggedExperiment, the ASCAT
data must undergo a number of operations to get it in the correct format for use
with RaggedExperiment.
if (!require("BiocManager"))
install.packages("BiocManager")
BiocManager::install("RaggedExperiment")Loading the package:
library(RaggedExperiment)
library(GenomicRanges)The data shown below is the output obtained from ASCAT. ASCAT takes Log R Ratio (LRR) and B Allele Frequency (BAF) files and derives the allele-specific copy number profiles of tumour cells, accounting for normal cell admixture and tumour aneuploidy. It should be noted that if working with raw CEL files, the first step is to preprocess the CEL files using the PennCNV-Affy pipeline described here. The PennCNV-Affy pipeline produces the LRR and BAF files used as inputs for ASCAT.
Depending on user preference, the output of ASCAT can be multiple files, each one containing allele-specific copy number information for one of the samples processed in an ASCAT run, or can be a single file containing allele-specific copy number information for all samples processed in an ASCAT run.
Let’s load up and have a look at ASCAT data that contains copy number information for just one sample i.e. sample1. Here we load up the data, check that it only contains allele-specific copy number calls for 1 sample and look at the first 10 rows of the dataframe.
ASCAT_data_S1 <- read.delim(
system.file(
"extdata", "ASCAT_Sample1.txt",
package = "RaggedExperiment", mustWork = TRUE
),
header = TRUE
)
unique(ASCAT_data_S1$sample)## [1] "sample1"head(ASCAT_data_S1, n = 10)## sample chr startpos endpos nMajor nMinor
## 1 sample1 1 61735 152555527 1 1
## 2 sample1 1 152555706 152586540 0 0
## 3 sample1 1 152586576 152761923 1 1
## 4 sample1 1 152761939 152768700 0 0
## 5 sample1 1 152773905 249224388 1 1
## 6 sample1 2 12784 32630548 1 1
## 7 sample1 2 32635284 33331778 2 1
## 8 sample1 2 33333871 243089456 1 1
## 9 sample1 3 60345 197896118 1 1
## 10 sample1 4 12281 191027923 1 1Now let’s load up and have a look at ASCAT data that contains copy number information for the three processed samples i.e. sample1, sample2 and sample3. Here we load up the data, check that it contains allele-specific copy number calls for the 3 samples and look at the first 10 rows of the dataframe. We also note that as expected the copy number calls for sample1 are the same as above.
ASCAT_data_All <- read.delim(
system.file(
"extdata", "ASCAT_All_Samples.txt",
package = "RaggedExperiment", mustWork = TRUE
),
header = TRUE
)
unique(ASCAT_data_All$sample)## [1] "sample1" "sample2" "sample3"head(ASCAT_data_All, n = 10)## sample chr startpos endpos nMajor nMinor
## 1 sample1 1 61735 152555527 1 1
## 2 sample1 1 152555706 152586540 0 0
## 3 sample1 1 152586576 152761923 1 1
## 4 sample1 1 152761939 152768700 0 0
## 5 sample1 1 152773905 249224388 1 1
## 6 sample1 2 12784 32630548 1 1
## 7 sample1 2 32635284 33331778 2 1
## 8 sample1 2 33333871 243089456 1 1
## 9 sample1 3 60345 197896118 1 1
## 10 sample1 4 12281 191027923 1 1From the output above we can see that the ASCAT data has 6 columns named sample, chr, startpos, endpos, nMajor and nMinor. These correspond to the sample ID, chromosome, the start position and end position of the genomic ranges and the copy number of the major and minor alleles i.e. the homologous chromosomes.
GRanges formatThe RaggedExperiment class derives from a GRangesList representation and can
take a GRanges object, a GRangesList or a list of Granges as inputs. To be
able to use the ASCAT data in RaggedExperiment we must convert the ASCAT data
into GRanges format. Ideally, we want each of our GRanges objects to
correspond to an individual sample.
GRanges objectsIn the case where the ASCAT data has only 1 sample it is relatively simple to
produce a GRanges object.
sample1_ex1 <- GRanges(
seqnames = Rle(paste0("chr", ASCAT_data_S1$chr)),
ranges = IRanges(start = ASCAT_data_S1$startpos, end = ASCAT_data_S1$endpos),
strand = Rle(strand("*")),
nmajor = ASCAT_data_S1$nMajor,
nminor = ASCAT_data_S1$nMinor
)
sample1_ex1## GRanges object with 41 ranges and 2 metadata columns:
## seqnames ranges strand | nmajor nminor
## <Rle> <IRanges> <Rle> | <integer> <integer>
## [1] chr1 61735-152555527 * | 1 1
## [2] chr1 152555706-152586540 * | 0 0
## [3] chr1 152586576-152761923 * | 1 1
## [4] chr1 152761939-152768700 * | 0 0
## [5] chr1 152773905-249224388 * | 1 1
## ... ... ... ... . ... ...
## [37] chr21 10736871-48096957 * | 1 1
## [38] chr22 16052528-51234455 * | 1 1
## [39] chrX 168477-54984266 * | 1 1
## [40] chrX 54988163-66944988 * | 2 0
## [41] chrX 66945740-155233846 * | 1 1
## -------
## seqinfo: 23 sequences from an unspecified genome; no seqlengthsHere we create a GRanges object by taking each column of the ASCAT data and
assigning them to the appropriate argument in the GRanges function. From above
we can see that the chromosome information is prefixed with “chr” and becomes
the seqnames column, the start and end positions are combined into an IRanges
object and given to the ranges argument, the strand column contains a * for
each entry as we don’t have strand information and the metadata columns contain
the allele-specific copy number calls and are called nmajor and nminor. The
GRanges object we have just created contains 41 ranges (rows) and 2 metadata
columns.
Another way that we can easily convert our ASCAT data, containing 1 sample, to a
GRanges object is to use the makeGRangesFromDataFrame function from the
GenomicsRanges package. Here we indicate what columns in our data correspond
to the chromosome (given to the seqnames argument), start and end positions
(start.field and end.field arguments), whether to ignore strand information
and assign all entries * (ignore.strand) and also whether to keep the other
columns in the dataframe, nmajor and nminor, as metadata columns
(keep.extra.columns).
sample1_ex2 <- makeGRangesFromDataFrame(
ASCAT_data_S1[,-c(1)],
ignore.strand=TRUE,
seqnames.field="chr",
start.field="startpos",
end.field="endpos",
keep.extra.columns=TRUE
)
sample1_ex2## GRanges object with 41 ranges and 2 metadata columns:
## seqnames ranges strand | nMajor nMinor
## <Rle> <IRanges> <Rle> | <integer> <integer>
## [1] 1 61735-152555527 * | 1 1
## [2] 1 152555706-152586540 * | 0 0
## [3] 1 152586576-152761923 * | 1 1
## [4] 1 152761939-152768700 * | 0 0
## [5] 1 152773905-249224388 * | 1 1
## ... ... ... ... . ... ...
## [37] 21 10736871-48096957 * | 1 1
## [38] 22 16052528-51234455 * | 1 1
## [39] X 168477-54984266 * | 1 1
## [40] X 54988163-66944988 * | 2 0
## [41] X 66945740-155233846 * | 1 1
## -------
## seqinfo: 23 sequences from an unspecified genome; no seqlengthsIn the case where the ASCAT data contains more than 1 sample you can first use
the split function to split the whole dataframe into multiple dataframes, one
for each sample, and then create a GRanges object for each dataframe. Code to
split the dataframe, based on sample ID, is given below and then the same
procedure used to produce sample1_ex2 can be implemented to create the
GRanges object. Alternatively, an easier and more efficient way to do this is
to use the makeGRangesListFromDataFrame function from the GenomicsRanges
package. This will be covered in the next section.
sample_list <- split(
ASCAT_data_All,
f = ASCAT_data_All$sample
)GRangesList instanceTo produce a GRangesList instance from the ASCAT dataframe we can use the
makeGRangesListFromDataFrame function. This function takes the same arguments
as the makeGRangesFromDataFrame function used above, but also has an argument
specifying how the rows of the df are split (split.field). Here we will
split on sample. This function can be used in cases where the ASCAT data
contains only 1 sample or where it contains multiple samples.
Using makeGRangesListFromDataFrame to create a list of GRanges objects where
ASCAT data has only 1 sample:
sample_list_GRanges_ex1 <- makeGRangesListFromDataFrame(
ASCAT_data_S1,
ignore.strand=TRUE,
seqnames.field="chr",
start.field="startpos",
end.field="endpos",
keep.extra.columns=TRUE,
split.field = "sample"
)
sample_list_GRanges_ex1## GRangesList object of length 1:
## $sample1
## GRanges object with 41 ranges and 2 metadata columns:
## seqnames ranges strand | nMajor nMinor
## <Rle> <IRanges> <Rle> | <integer> <integer>
## [1] 1 61735-152555527 * | 1 1
## [2] 1 152555706-152586540 * | 0 0
## [3] 1 152586576-152761923 * | 1 1
## [4] 1 152761939-152768700 * | 0 0
## [5] 1 152773905-249224388 * | 1 1
## ... ... ... ... . ... ...
## [37] 21 10736871-48096957 * | 1 1
## [38] 22 16052528-51234455 * | 1 1
## [39] X 168477-54984266 * | 1 1
## [40] X 54988163-66944988 * | 2 0
## [41] X 66945740-155233846 * | 1 1
## -------
## seqinfo: 23 sequences from an unspecified genome; no seqlengthsUsing makeGRangesListFromDataFrame to create a list of GRanges objects
where ASCAT data has multiple samples:
sample_list_GRanges_ex2 <- makeGRangesListFromDataFrame(
ASCAT_data_All,
ignore.strand=TRUE,
seqnames.field="chr",
start.field="startpos",
end.field="endpos",
keep.extra.columns=TRUE,
split.field = "sample"
)
sample_list_GRanges_ex2## GRangesList object of length 3:
## $sample1
## GRanges object with 41 ranges and 2 metadata columns:
## seqnames ranges strand | nMajor nMinor
## <Rle> <IRanges> <Rle> | <integer> <integer>
## [1] 1 61735-152555527 * | 1 1
## [2] 1 152555706-152586540 * | 0 0
## [3] 1 152586576-152761923 * | 1 1
## [4] 1 152761939-152768700 * | 0 0
## [5] 1 152773905-249224388 * | 1 1
## ... ... ... ... . ... ...
## [37] 21 10736871-48096957 * | 1 1
## [38] 22 16052528-51234455 * | 1 1
## [39] X 168477-54984266 * | 1 1
## [40] X 54988163-66944988 * | 2 0
## [41] X 66945740-155233846 * | 1 1
## -------
## seqinfo: 23 sequences from an unspecified genome; no seqlengths
##
## $sample2
## GRanges object with 64 ranges and 2 metadata columns:
## seqnames ranges strand | nMajor nMinor
## <Rle> <IRanges> <Rle> | <integer> <integer>
## [1] 1 61735-238045995 * | 1 1
## [2] 1 238046253-249224388 * | 2 0
## [3] 2 12784-243089456 * | 1 1
## [4] 3 60345-197896118 * | 1 1
## [5] 4 12281-191027923 * | 1 1
## ... ... ... ... . ... ...
## [60] X 168477-18760388 * | 1 1
## [61] X 18761872-22174817 * | 2 0
## [62] X 22175673-55224760 * | 1 1
## [63] X 55230288-67062507 * | 2 0
## [64] X 67065988-155233846 * | 1 1
## -------
## seqinfo: 23 sequences from an unspecified genome; no seqlengths
##
## $sample3
## GRanges object with 30 ranges and 2 metadata columns:
## seqnames ranges strand | nMajor nMinor
## <Rle> <IRanges> <Rle> | <integer> <integer>
## [1] 1 61735-121482979 * | 2 0
## [2] 1 144007049-249224388 * | 2 2
## [3] 2 12784-243089456 * | 2 0
## [4] 3 60345-197896118 * | 2 0
## [5] 4 12281-191027923 * | 2 0
## ... ... ... ... . ... ...
## [26] 20 61305-62956153 * | 2 2
## [27] 21 10736871-44320760 * | 2 0
## [28] 21 44320989-48096957 * | 3 0
## [29] 22 16052528-51234455 * | 2 0
## [30] X 168477-155233846 * | 2 2
## -------
## seqinfo: 23 sequences from an unspecified genome; no seqlengthsEach GRanges object in the list can then be accessed using square bracket
notation.
sample1_ex3 <- sample_list_GRanges_ex2[[1]]
sample1_ex3## GRanges object with 41 ranges and 2 metadata columns:
## seqnames ranges strand | nMajor nMinor
## <Rle> <IRanges> <Rle> | <integer> <integer>
## [1] 1 61735-152555527 * | 1 1
## [2] 1 152555706-152586540 * | 0 0
## [3] 1 152586576-152761923 * | 1 1
## [4] 1 152761939-152768700 * | 0 0
## [5] 1 152773905-249224388 * | 1 1
## ... ... ... ... . ... ...
## [37] 21 10736871-48096957 * | 1 1
## [38] 22 16052528-51234455 * | 1 1
## [39] X 168477-54984266 * | 1 1
## [40] X 54988163-66944988 * | 2 0
## [41] X 66945740-155233846 * | 1 1
## -------
## seqinfo: 23 sequences from an unspecified genome; no seqlengthsAnother way we can produce a GRangesList instance is to use the GRangesList
function. This function creates a list that contains all our GRanges objects.
This is straightforward in that we use the GRangesList function with our
GRanges objects as named or unnamed inputs. Below we have created a list that
includes 1 GRanges objects, created in section 4.1., corresponding to sample1.
sample_list_GRanges_ex3 <- GRangesList(
sample1 = sample1_ex1
)
sample_list_GRanges_ex3## GRangesList object of length 1:
## $sample1
## GRanges object with 41 ranges and 2 metadata columns:
## seqnames ranges strand | nmajor nminor
## <Rle> <IRanges> <Rle> | <integer> <integer>
## [1] chr1 61735-152555527 * | 1 1
## [2] chr1 152555706-152586540 * | 0 0
## [3] chr1 152586576-152761923 * | 1 1
## [4] chr1 152761939-152768700 * | 0 0
## [5] chr1 152773905-249224388 * | 1 1
## ... ... ... ... . ... ...
## [37] chr21 10736871-48096957 * | 1 1
## [38] chr22 16052528-51234455 * | 1 1
## [39] chrX 168477-54984266 * | 1 1
## [40] chrX 54988163-66944988 * | 2 0
## [41] chrX 66945740-155233846 * | 1 1
## -------
## seqinfo: 23 sequences from an unspecified genome; no seqlengthsRaggedExperiment object from ASCAT outputNow we have created the GRanges objects and GRangesList instances we can
easily use RaggedExperiment.
GRanges objectsFrom above we have a GRanges object derived from the ASCAT data containing 1
sample i.e. sample1_ex1 / sample1_ex2 and the capabilities to produce
individual GRanges objects derived from the ASCAT data containing 3 samples.
We can now use these GRanges objects as inputs to RaggedExperiment. Note
that we create column data colData to describe the samples.
Using GRanges object where ASCAT data only has 1 sample:
colDat_1 = DataFrame(id = 1)
ragexp_1 <- RaggedExperiment(
sample1 = sample1_ex2,
colData = colDat_1
)
ragexp_1## class: RaggedExperiment
## dim: 41 1
## assays(2): nMajor nMinor
## rownames: NULL
## colnames(1): sample1
## colData names(1): idIn the case where you have multiple GRanges objects, corresponding to
different samples, the code is similar to above. Each sample is inputted into
the RaggedExperiment function and colDat_1 corresponds to the id for each
sample i.e. 1, 2 and 3, if 3 samples are provided.
GRangesList instanceFrom before we have a GRangesList derived from the ASCAT data containing 1
sample i.e. sample_list_GRanges_ex1 and the GRangesList derived from the
ASCAT data containing 3 samples i.e. sample_list_GRanges_ex2. We can now use
this GRangesList as the input to RaggedExperiment.
Using GRangesList where ASCAT data only has 1 sample:
ragexp_2 <- RaggedExperiment(
sample_list_GRanges_ex1,
colData = colDat_1
)
ragexp_2## class: RaggedExperiment
## dim: 41 1
## assays(2): nMajor nMinor
## rownames: NULL
## colnames(1): sample1
## colData names(1): idUsing GRangesList where ASCAT data only has multiple samples:
colDat_3 = DataFrame(id = 1:3)
ragexp_3 <- RaggedExperiment(
sample_list_GRanges_ex2,
colData = colDat_3
)
ragexp_3## class: RaggedExperiment
## dim: 135 3
## assays(2): nMajor nMinor
## rownames: NULL
## colnames(3): sample1 sample2 sample3
## colData names(1): idWe can also use the GRangesList produced using the GRangesList function:
ragexp_4 <- RaggedExperiment(
sample_list_GRanges_ex3,
colData = colDat_1
)
ragexp_4## class: RaggedExperiment
## dim: 41 1
## assays(2): nmajor nminor
## rownames: NULL
## colnames(1): sample1
## colData names(1): idNow that we have the ASCAT data converted to RaggedExperiment objects we can
use the *Assay functions that are described in the RaggedExperiment
vignette.
These functions provide several different functions for representing ranged data
in a rectangular matrix. They make it easy to find genomic segments shared/not
shared between each sample considered and provide the corresponding
allele-specific copy number calls for each sample across each segment.
sessionInfo()## R version 4.3.1 (2023-06-16)
## Platform: x86_64-pc-linux-gnu (64-bit)
## Running under: Ubuntu 22.04.3 LTS
##
## Matrix products: default
## BLAS: /home/biocbuild/bbs-3.18-bioc/R/lib/libRblas.so
## LAPACK: /usr/lib/x86_64-linux-gnu/lapack/liblapack.so.3.10.0
##
## locale:
## [1] LC_CTYPE=en_US.UTF-8 LC_NUMERIC=C
## [3] LC_TIME=en_GB LC_COLLATE=C
## [5] LC_MONETARY=en_US.UTF-8 LC_MESSAGES=en_US.UTF-8
## [7] LC_PAPER=en_US.UTF-8 LC_NAME=C
## [9] LC_ADDRESS=C LC_TELEPHONE=C
## [11] LC_MEASUREMENT=en_US.UTF-8 LC_IDENTIFICATION=C
##
## time zone: America/New_York
## tzcode source: system (glibc)
##
## attached base packages:
## [1] stats4 stats graphics grDevices utils datasets methods
## [8] base
##
## other attached packages:
## [1] RaggedExperiment_1.26.0 GenomicRanges_1.54.0 GenomeInfoDb_1.38.0
## [4] IRanges_2.36.0 S4Vectors_0.40.0 BiocGenerics_0.48.0
## [7] BiocStyle_2.30.0
##
## loaded via a namespace (and not attached):
## [1] Matrix_1.6-1.1 jsonlite_1.8.7
## [3] compiler_4.3.1 BiocManager_1.30.22
## [5] crayon_1.5.2 BiocBaseUtils_1.4.0
## [7] SummarizedExperiment_1.32.0 Biobase_2.62.0
## [9] bitops_1.0-7 jquerylib_0.1.4
## [11] yaml_2.3.7 fastmap_1.1.1
## [13] lattice_0.22-5 R6_2.5.1
## [15] XVector_0.42.0 S4Arrays_1.2.0
## [17] knitr_1.44 DelayedArray_0.28.0
## [19] bookdown_0.36 MatrixGenerics_1.14.0
## [21] GenomeInfoDbData_1.2.11 bslib_0.5.1
## [23] rlang_1.1.1 cachem_1.0.8
## [25] xfun_0.40 sass_0.4.7
## [27] SparseArray_1.2.0 cli_3.6.1
## [29] zlibbioc_1.48.0 digest_0.6.33
## [31] grid_4.3.1 evaluate_0.22
## [33] abind_1.4-5 RCurl_1.98-1.12
## [35] rmarkdown_2.25 matrixStats_1.0.0
## [37] tools_4.3.1 htmltools_0.5.6.1