Progenetix is an open data resource that provides curated individual cancer copy number variation (CNV) profiles along with associated metadata sourced from published oncogenomic studies and various data repositories. This vignette provides a comprehensive guide on accessing genomic variant data within the Progenetix database.
If your focus lies in cancer cell lines, you can access data from cancercelllines.org by
setting the domain parameter to “https://cancercelllines.org” in pgxLoader
function. This data repository originates from CNV profiling data of
cell lines initially collected as part of Progenetix and currently
includes additional types of genomic mutations.
library(pgxRpi)
library(SummarizedExperiment) # for pgxmatrix data
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#> anyMissing, rowMedianspgxLoader functionThis function loads various data from Progenetix
database via the Beacon v2 API with some extensions (BeaconPlus).
The parameters of this function used in this tutorial:
type: A string specifying output data type.
“g_variants” and “cnv_fraction” are used in this tutorial.output: A string specifying output file format. The
available options depend on the type parameter. When
type is “g_variants”, available options are NULL (default),
“pgxseg”, or “seg”; when type is “cnv_fraction”, available
options are NULL (default) or “pgxmatrix”.biosample_id: Identifiers used in the query database
for identifying biosamples.individual_id: Identifiers used in the query database
for identifying individuals.filters: Identifiers used in public repositories,
bio-ontology terms, or custom terms such as c(“NCIT:C7376”,
“PMID:22824167”). For more information about filters, see the documentation.codematches: A logical value determining whether to
exclude samples from child concepts of specified filters in the ontology
tree. If TRUE, only samples exactly matching the specified filters will
be included. Do not use this parameter when filters include
ontology-irrelevant filters such as PMID and cohort identifiers. Default
is FALSE.limit: Integer to specify the number of returned
profiles. Default is 0 (return all).skip: Integer to specify the number of skipped
profiles. E.g. if skip = 2, limit=500, the first 2*500 =1000 profiles
are skipped and the next 500 profiles are returned. Default is NULL (no
skip).dataset: A string specifying the dataset to query from
the Beacon response. Default is NULL, which includes results from all
datasets.save_file: A logical value determining whether to save
variant data as a local file instead of direct return. Only used when
the parameter type is “g_variants”. Default is FALSE.filename: A string specifying the path and name of the
file to be saved. Only used if the parameter save_file is
TRUE. Default is “variants” in current work directory.num_cores: Integer to specify the number of cores used
for the variant query. Only used when the parameter type is
“g_variants”. Default is 1.domain: A string specifying the domain of the query
data resource. Default is “http://progenetix.org”.entry_point: A string specifying the entry point of the
Beacon v2 API. Default is “beacon”, resulting in the endpoint being “http://progenetix.org/beacon”.Because of a time-out issue, segment variant data can only be
accessed by biosample id instead of filters. To speed up this process,
you can set the num_cores parameter for parallel
processing. For more information about filters and how to get biosample
ids, see the vignette Introduction_1_loadmetadata.
# get 2 samples for demonstration
biosamples <- pgxLoader(type="biosamples", filters = "PMID:20229506", limit=2)
biosample_id <- biosamples$biosample_id
biosample_id
#> [1] "pgxbs-kftviq25" "pgxbs-kftviq27"There are three output formats.
The default output format extracts variant data from the Beacon v2 response, containing variant id and associated analysis id, biosample id and individual id. The CNV data is represented as copy number change class following the GA4GH Variation Representation Specification (VRS).
variant_1 <- pgxLoader(type="g_variants", biosample_id = biosample_id)
head(variant_1)
#> variant_id analysis_id biosample_id individual_id
#> 1 pgxvar-66577cf9b44ee5c2598e5148 pgxcs-kftwah0f pgxbs-kftviq25 pgxind-kftx4g36
#> 2 pgxvar-66577cf9b44ee5c2598e5149 pgxcs-kftwah0f pgxbs-kftviq25 pgxind-kftx4g36
#> 3 pgxvar-66577cf9b44ee5c2598e514a pgxcs-kftwah0f pgxbs-kftviq25 pgxind-kftx4g36
#> 4 pgxvar-66577cf9b44ee5c2598e514b pgxcs-kftwah0f pgxbs-kftviq25 pgxind-kftx4g36
#> 5 pgxvar-66577cf9b44ee5c2598e514c pgxcs-kftwah0f pgxbs-kftviq25 pgxind-kftx4g36
#> 6 pgxvar-66577cf9b44ee5c2598e514d pgxcs-kftwah0f pgxbs-kftviq25 pgxind-kftx4g36
#> variant_internal_id sequence_id start end
#> 1 1:1731500-12832655:EFO_0030068 refseq:NC_000001.11 1731500 12832655
#> 2 1:12849386-57712606:EFO_0030068 refseq:NC_000001.11 12849386 57712606
#> 3 1:57713043-64335282:EFO_0030068 refseq:NC_000001.11 57713043 64335282
#> 4 1:64338058-68715276:EFO_0030068 refseq:NC_000001.11 64338058 68715276
#> 5 1:68716685-72284670:EFO_0030068 refseq:NC_000001.11 68716685 72284670
#> 6 1:72303254-77320849:EFO_0030068 refseq:NC_000001.11 72303254 77320849
#> variant_copychange
#> 1 EFO:0030068
#> 2 EFO:0030068
#> 3 EFO:0030068
#> 4 EFO:0030068
#> 5 EFO:0030068
#> 6 EFO:0030068output = “pgxseg”)This format accesses data from Progenetix API
services. The ‘.pgxseg’ file format contains segment mean values (in
log2 column), which are equal to log2(copy number of
measured sample/copy number of control sample (usually 2)). A few
variants are point mutations represented by columns
reference_bases and alternate_bases.
variant_2 <- pgxLoader(type="g_variants", biosample_id = biosample_id,output = "pgxseg")
head(variant_2)
#> biosample_id reference_name start end log2 variant_type
#> 1 pgxbs-kftviq25 1 1731500 12832655 -0.4922 DEL
#> 2 pgxbs-kftviq25 1 12849386 57712606 -0.4888 DEL
#> 3 pgxbs-kftviq25 1 57713043 64335282 -0.4254 DEL
#> 4 pgxbs-kftviq25 1 64338058 68715276 -0.4098 DEL
#> 5 pgxbs-kftviq25 1 68716685 72284670 -0.3219 DEL
#> 6 pgxbs-kftviq25 1 72303254 77320849 -0.3330 DEL
#> reference_bases alternate_bases variant_state_id variant_state_label
#> 1 . . EFO:0030068 low-level copy number loss
#> 2 . . EFO:0030068 low-level copy number loss
#> 3 . . EFO:0030068 low-level copy number loss
#> 4 . . EFO:0030068 low-level copy number loss
#> 5 . . EFO:0030068 low-level copy number loss
#> 6 . . EFO:0030068 low-level copy number lossoutput = “seg”)This format accesses data from Progenetix API services. This format is similar to the general ‘.seg’ file format and compatible with IGV tool for visualization. The only difference between this file format and the general ‘.seg’ file format is the fifth column. It represents variant type in this format while in the general ‘.seg’ file format, it represents number of probes or bins covered by the segment.
variant_3 <- pgxLoader(type="g_variants", biosample_id = biosample_id,output = "seg")
head(variant_3)
#> biosample_id reference_name start end variant_type log2
#> 1 pgxbs-kftviq25 1 1731500 12832655 DEL -0.4922
#> 2 pgxbs-kftviq25 1 12849386 57712606 DEL -0.4888
#> 3 pgxbs-kftviq25 1 57713043 64335282 DEL -0.4254
#> 4 pgxbs-kftviq25 1 64338058 68715276 DEL -0.4098
#> 5 pgxbs-kftviq25 1 68716685 72284670 DEL -0.3219
#> 6 pgxbs-kftviq25 1 72303254 77320849 DEL -0.3330Setting save_file to TRUE in the pgxLoader
function will save the retrieved variants data to a file rather than
returning it directly. By default, the data will be saved in the current
working directory, but you can specify a different path using the
filename parameter. This export functionality is only
available for variants data (when type='g_variants').
The following command creates a ‘.pgxseg’ file with the name “variants.pgxseg” in “~/Downloads/” folder.
pgxLoader(type="g_variants", output="pgxseg", biosample_id=biosample_id, save_file=TRUE,
filename="~/Downloads/variants.pgxseg")To visualize the ‘.pgxseg’ file, you can either upload it to this link or use the byconaut package for local visualization when dealing with a large number of samples.
The following command creates a special ‘.seg’ file with the name “variants.seg” in “~/Downloads/” folder.
pgxLoader(type="g_variants", output="seg", biosample_id=biosample_id, save_file=TRUE,
filename="~/Downloads/variants.seg")You can upload this ‘.seg’ file to IGV tool for visualization.
Because segment variants are not harmonized across samples,
Progenetix provides processed CNV features, known as CNV fractions.
These fractions represent the proportion of genomic regions overlapping
one or more CNVs of a given type, facilitating sample-wise comparisons.
The following query is based on filters, but biosample id and individual
id are also available for sample-specific CNV fraction queries. For more
information about filters, biosample id and individual id, as well as
the use of parameters skip, limit, and
codematches, see the vignette
Introduction_1_loadmetadata.
This includes CNV fraction across chromosome arms, whole chromosomes, or the whole genome.
The CNV fraction across chromosomal arms looks like this
head(cnv_fraction$arm_cnv_frac)[,c(1:4, 49:52)]
#> chr1p.dup chr1q.dup chr2p.dup chr2q.dup chr1p.del chr1q.del
#> pgxcs-kftvs0ri 0 0.000 0.000 0.000 0.000 0
#> pgxcs-kftvu9w2 0 0.000 0.000 0.000 0.000 0
#> pgxcs-kftvw1kw 0 0.000 0.000 0.000 0.000 0
#> pgxcs-kftvw1ld 0 0.000 0.000 0.000 0.000 0
#> pgxcs-kftvw1lu 0 0.000 0.000 0.000 0.225 0
#> pgxcs-kftvw1mb 0 0.979 0.989 0.003 0.000 0
#> chr2p.del chr2q.del
#> pgxcs-kftvs0ri 0 0
#> pgxcs-kftvu9w2 0 0
#> pgxcs-kftvw1kw 0 0
#> pgxcs-kftvw1ld 0 0
#> pgxcs-kftvw1lu 0 0
#> pgxcs-kftvw1mb 0 0The row names are analyses ids from samples that belong to the input filter NCIT:C2948. There are 96 columns. The first 48 columns are duplication fraction across chromosomal arms, followed by deletion fraction. CNV fraction across whole chromosomes is similar, with the only difference in columns.
The CNV fraction across the genome (hg38) looks like this
head(cnv_fraction$genome_cnv_frac)
#> cnvfraction dupfraction delfraction
#> pgxcs-kftvs0ri 0.080 0.036 0.044
#> pgxcs-kftvu9w2 0.058 0.010 0.048
#> pgxcs-kftvw1kw 0.000 0.000 0.000
#> pgxcs-kftvw1ld 0.000 0.000 0.000
#> pgxcs-kftvw1lu 0.027 0.000 0.027
#> pgxcs-kftvw1mb 0.176 0.159 0.017The first column is the total called fraction, followed by duplication fraction and deletion fraction.
The returned data is stored in RangedSummarizedExperiment object, which is a matrix-like container where rows represent ranges of interest (as a GRanges object) and columns represent analyses derived from biosamples. The data looks like this
cnvfrac_matrix
#> class: RangedSummarizedExperiment
#> dim: 6212 47
#> metadata(0):
#> assays(1): cnv_matrix
#> rownames(6212): 1 2 ... 6211 6212
#> rowData names(1): type
#> colnames(47): pgxcs-kftvs0ri pgxcs-kftvu9w2 ... pgxcs-khv36qld
#> pgxcs-khv36qnu
#> colData names(3): analysis_id biosample_id group_idYou could get the interval information by rowRanges
function from SummarizedExperiment package.
rowRanges(cnvfrac_matrix)
#> GRanges object with 6212 ranges and 1 metadata column:
#> seqnames ranges strand | type
#> <Rle> <IRanges> <Rle> | <character>
#> 1 chr1 0-400000 * | DUP
#> 2 chr1 400000-1400000 * | DUP
#> 3 chr1 1400000-2400000 * | DUP
#> 4 chr1 2400000-3400000 * | DUP
#> 5 chr1 3400000-4400000 * | DUP
#> ... ... ... ... . ...
#> 6208 chrY 52400000-53400000 * | DEL
#> 6209 chrY 53400000-54400000 * | DEL
#> 6210 chrY 54400000-55400000 * | DEL
#> 6211 chrY 55400000-56400000 * | DEL
#> 6212 chrY 56400000-57227415 * | DEL
#> -------
#> seqinfo: 24 sequences from an unspecified genome; no seqlengthsTo access the CNV fraction matrix, use assay accesssor
from SummarizedExperiment package
assay(cnvfrac_matrix)[1:3,1:3]
#> pgxcs-kftvs0ri pgxcs-kftvu9w2 pgxcs-kftvw1kw
#> 1 0 0 0
#> 2 0 0 0
#> 3 0 0 0The matrix has 6212 rows (genomic regions) and 47 columns (analysis profiles derived from samples belonging to the input filter). The rows comprised 3106 intervals with “gain status” plus 3106 intervals with “loss status”.
The value is the fraction of the binned interval overlapping with one or more CNVs of the given type (DUP/DEL). For example, if the value in the second row, the first column is 0.2, it means that one or more duplication events overlapped with 20% of the genomic bin located in chromosome 1: 400000-1400000 in the first analysis profile.
To get associated biosample id and filters for analyses, use
colData function from SummarizedExperiment
package:
colData(cnvfrac_matrix)
#> DataFrame with 47 rows and 3 columns
#> analysis_id biosample_id group_id
#> <character> <character> <character>
#> pgxcs-kftvs0ri pgxcs-kftvs0ri pgxbs-kftvh262 NCIT:C2948
#> pgxcs-kftvu9w2 pgxcs-kftvu9w2 pgxbs-kftvh9fp NCIT:C2948
#> pgxcs-kftvw1kw pgxcs-kftvw1kw pgxbs-kftvhf4h NCIT:C8893
#> pgxcs-kftvw1ld pgxcs-kftvw1ld pgxbs-kftvhf4i NCIT:C8893
#> pgxcs-kftvw1lu pgxcs-kftvw1lu pgxbs-kftvhf4k NCIT:C8893
#> ... ... ... ...
#> pgxcs-kftwzzn7 pgxcs-kftwzzn7 pgxbs-kftvl7bn NCIT:C2948
#> pgxcs-khv36qi3 pgxcs-khv36qi3 pgxbs-khv36qhj NCIT:C2948
#> pgxcs-khv36qjf pgxcs-khv36qjf pgxbs-khv36qiw NCIT:C2948
#> pgxcs-khv36qld pgxcs-khv36qld pgxbs-khv36qku NCIT:C2948
#> pgxcs-khv36qnu pgxcs-khv36qnu pgxbs-khv36qnb NCIT:C2948analysis_id is the identifier for individual analysis,
biosample_id is the identifier for individual biosample. It
is noted that the number of analysis profiles does not necessarily equal
the number of samples. One biosample id may correspond to multiple
analysis ids. group_id corresponds to the meaning of
filters.
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