RGMQL: GenoMetric Query Language for R/Bioconductor
Simone Pallotta
Marco Masseroli
2022-04-26
Introduction
Recent years have seen a tremendous increase in the volume of data generated in the life sciences, especially propelled by the rapid progress of Next Generation Sequencing (NGS) technologies. These high-throughput technologies can produce billions of short DNA or RNA fragments in excess of a few terabytes of data in a single run. Next-generation sequencing refers to the deep, in-parallel DNA sequencing technologies providing massively parallel analysis and extremely high-throughput from multiple samples at much reduced cost. Improvement of sequencing technologies and data processing pipelines is rapidly providing sequencing data, with associated high-level features, of many individual genomes in multiple biological and clinical conditions. To make effective use of the produced data, the design of big data algorithms and their efficient implementation on modern high performance computing infrastructures, such as clouds, CPU clusters and network infrastructures, is required in order to achieve scalability and performance. For this purpose, the GenoMetric Query Language (GMQL) has been proposed as high-level, declarative language to process, query, and compare multiple and heterogeneous genomic datasets for biomedical knowledge discovery1
Purpose
A very important emerging problem is to make sense of the enormous amount and variety of NGS data becoming available, i.e., to discover how different genomic regions and their products interact and cooperate with each other. To this aim, the integration of several heterogeneous DNA feature data is required. Such big genomic feature data are collected within numerous and heterogeneous files, usually distributed within different repositories, lacking an attribute-based organization and a systematic description of their metadata. These heterogeneous data can contain the hidden answers to very important biomedical questions. To unveil them, standard tools already available for knowledge extraction are too specialized or present powerful features, but have a rough interface not well-suited for scientists/biologists. GMQL addresses these aspects using cloud-based technologies (including Apache Hadoop, mapReduce, and Spark), and focusing on genomic data operations written as simple queries with implicit iterations over thousands of heterogeneous samples, computed efficiently2. This RGMQL package makes easy to take advantage of GMQL functionalities also to scientists and biologists with limited knowledge of query and programming languages, but used to the R/Bioconductor environment. This package is built over a GMQL scalable data management engine written in Scala programming language, released as Scala API3 providing a set of functions to combine, manipulate, compare, and extract heterogenous genomic data collected both on local and remote datasets and thus coming from different data sources. These functions, built extending functionalities available in the R/Bioconductor framework, allow performing complex GMQL processing and queries without knowledge of GMQL syntax, but leveraging on R idiomatic paradigm and logic. Additionally, RGMQL allows to use indistinctly local processing on the user machine and remote query outsourcing (i.e. assign the computations to a remote GMQL service), in both cases working seamlessly on local or remote data.
Genomic Data Model
The Genomic Data Model (GDM) is based on the notions of datasets and samples4 Datasets are collections of samples, and each sample consists of two parts, the region data, which describe portions of the genome, and the metadata, which describe sample general properties and how observations are collected. In contrast to other data models, it clearly divides, and comprehensively manages, observations about genomic regions and metadata. GDM provides a flat attribute based organization, just requiring that each dataset is associated with a given data schema, which specifies the attributes and their type of region data. The first attributes of such schema are fixed (chr, start, stop strand); they represent the genomic region identifying coordinates. In addition, metadata have free attribute-value pair format.
Genomic Region
Genomic region data describe a broad variety of biomolecular aspects and are very valuable for biomolecular investigation. A genomic region is a portion of a genome, qualified by a quadruple of values called region coordinates: \[< chr, start, stop, strand >\]Regions can have associated an arbitrary number of attributes with their value, according to the processing of DNA, RNA or epigenomic sequencing reads that determined the region.
Metadata
Metadata describe the biological and clinical properties associated with each sample. They are usually collected in a broad variety of data structures and formats that constitute barriers to their use and comparison. GDM models metadata simply as arbitrary semi-structured attribute-value pairs, where attributes may have multiple values.
Genomic Sample
Formally, a sample \(s\) is a collection of genomic regions modelled as the following triple: \[< id, {< r_i,v_i >}, {m_j} >\] where:
- \(id\) is the sample identifier
- Each region is a pair of coordinates \(r_i\) and values \(v_i\)
- Metadata \(m_j\) are attribute-value pairs \(< a_j,v_j >\)
Note that the sample \(id\) attribute provides a many-to-many connection between regions and metadata of a sample. Through the use of a data type system to express region data, and of arbitrary attribute-value pairs for metadata, GDM provides interoperability across datasets in multiple formats produced by different experimental techniques.
Dataset
A dataset is a collection of samples uniquely identified, with the same region schema and with each sample consisting of two parts:
- region data: describing characteristics and location of genomic portions
- metadata: expressing general properties of the sample
Each dataset is typically produced within the same project by using the same or equivalent technology and tools, but with different experimental conditions, described by metadata.
Datasets contain large number of information describing regions of a genome, with data encoded in human readable format using plain text files.
GMQL datasets are materialized in a standard layout composed of three types of files:
- genomic region tab-delimited text files with extension .gdm, or .gtf if in standard GTF format
- metadata attribute-value tab-delimited text files with the same fullname (name and extension) of the correspondent genomic region file and extension .meta
- schema XML file containing region attribute names and types
All these files reside in a unique folder called \(files\).
In RGMQL package, dataset files are considered read-only. Once read, genomic information is represented in an abstract data structure inside the package, mapped to a R GRanges data structure as needed for optimal use and interoperability with all available R/Bioconductor functions.
GenoMetric Query Language
The GenoMetric Query Language name stems from such language ability to deal with genomic distances, which are measured as number of nucleotide bases between genomic regions (aligned to the same reference genome) and computed using arithmetic operations between region coordinates. GMQL is a high-level, declarative language that allows expressing queries easily over genomic regions and their metadata, in a way similar to what can be done with the Structured Query Language (SQL) over a relational database. GMQL approach exhibits two main differences with respect to other tools based on Hadoop, mapReduce framework, and Spark engine technologies to address similar biomedical problems:
GMQL:
- reads from processed datasets
- supports metadata management
Others:
- read generally from raw or aligned data from NGS machines
- provide no support for metadata management
GMQL is the appropriate tool for querying many genomic datasets and very many samples of numerous processed genomic region data that are becoming available. Note however that GMQL performs worse than some other available systems on a small number of small-scale datasets, but these other systems are not cloud-based; hence, they are not adequate for efficient big data processing and, in some cases, they are inherently limited in their data management capacity, as they only work as RAM memory resident processes.
GMQL Query Structure
A GMQL query, or script, is expressed as a sequence of GMQL operations with the following structure: \[< variable > = operator(< parameters >) < variable >;\] where each \(< variable >\) stands for a GDM dataset
This RGMQL package brings GMQL functionalities into R environment, allowing users to build directly a GMQL query without knowing the GMQL syntax, but using R idiomatic expressions and available R functions suitably extended. In RGMQL every GMQL operations is translated into a R function and expressed as: \[ variable = operator(variable, parameters)\]
It is very similar to the GMQL syntax for operation expression, although expressed with the R idiomatic paradigm and logic, with parameters totally built using R native data structures such as lists, matrices, vectors or R logic conditions.
Processing Environments
In this section, we show how GMQL processing is built in R, which operations are available in RGMQL, and the difference between local and remote dataset processing.
Local Processing
RGMQL local processing consumes computational power directly from local CPUs/system while managing datasets (both GMQL or generic text plain datasets).
Initialization
Load and attach the RGMQL package in a R session using library function:
library('RGMQL')## Loading required package: RGMQLlib## GMQL successfully loadedRGMQL depends on another package called RGMQLlib automatically installed when installing RGMQL and loaded each time RGMQL is loaded ; if not, you can install it from Bioconductor and load it using:
library('RGMQLlib')Before starting using any GMQL operation we need to initialise the GMQL context with the following code:
init_gmql()The function init_gmql() initializes the context of scalable data management engine laid upon Spark and Hadoop, and the format of materialized result datasets. Details on this and all other functions are provided in the R documentation for this package (i.e., help(RGMQL)).
Read Dataset
After initialization, we need to read datasets. We already defined above the formal definition of dataset and the power of GMQL and its Genomic Data Model to deal with data in a variety of common tab-delimited text formats, among which SAM (Sequence Alignment/Map), VCF (Variant Call Format), NARROWPEAK (for called peaks produced by NGS ChIP-seq or DNase-seq methods) and BED (Browser Extensible Data) formats, as well all the formats describing experimental datasets (e.g., copy number variations, DNA somatic mutations, or gene expressions) and annotations (e.g., about transcription start sites, genes, enhancers or CpG islands).
In the following, we show how to get data from different sources.
We distinguish two different cases:
- Local dataset:A local dataset is a folder with sample files (region files and correspondent metadata files) on the user computer. As data are already in the user computer, we simply execute:
gmql_dataset_path <- system.file("example", "EXON", package = "RGMQL")
data_out = read_gmql(gmql_dataset_path)In this case we are reading a GMQL dataset specified by the path of its folder “EXON” within the subdirectory “example” of the package “RGMQL”. It does not matter what kind of format the data are, read_gmql() reads many standard tab-delimited text formats without the need of specifying any additional input parameter.
- GRangesList:For better integration in the R environment and with other R packages, we provide the read_GRangesList() function to read directly from R memory using GRangesList as input.
library("GenomicRanges")## Loading required package: stats4## Loading required package: BiocGenerics##
## Attaching package: 'BiocGenerics'## The following objects are masked from 'package:stats':
##
## IQR, mad, sd, var, xtabs## The following objects are masked from 'package:base':
##
## Filter, Find, Map, Position, Reduce, anyDuplicated, append,
## as.data.frame, basename, cbind, colnames, dirname, do.call,
## duplicated, eval, evalq, get, grep, grepl, intersect, is.unsorted,
## lapply, mapply, match, mget, order, paste, pmax, pmax.int, pmin,
## pmin.int, rank, rbind, rownames, sapply, setdiff, sort, table,
## tapply, union, unique, unsplit, which.max, which.min## Loading required package: S4Vectors##
## Attaching package: 'S4Vectors'## The following objects are masked from 'package:base':
##
## I, expand.grid, unname## Loading required package: IRanges## Loading required package: GenomeInfoDb# Granges Object with one region: chr2 and two metadata columns: score = 5
# and GC = 0.45
gr1 <- GRanges(seqnames = "chr2",
ranges = IRanges(103, 106), strand = "+", score = 5, GC = 0.45)
# Granges Object with two regions both chr1 and two metadata columns: score = 3
# for the fist region and score = 4 for the second one, GC = 0.3 and 0.5
# for the first and second region, respectively
gr2 <- GRanges(seqnames = c("chr1", "chr1"),
ranges = IRanges(c(107, 113), width = 3), strand = c("+", "-"),
score = 3:4, GC = c(0.3, 0.5))
grl <- GRangesList("txA" = gr1, "txB" = gr2)
data_out <- read_GRangesList(grl)## Warning in read_GRangesList(grl): No metadata.
## We provide two metadata for you:
##
## 1.provider = PoliMi
## 2.application = RGMQLIn this example we show how versatile the RGMQL package is. As specified above, we can directly read a list of GRanges previously created starting from two GRanges. Both read_GRangesList() and read_gmql() functions return a result object, in this case data_out: an instance of GMQLDataset class used as input for executing the subsequent GMQL operation.NOTE: if grl@metadata is empty, the function provides two default metadata:
- “provider” = “PoliMi”
- “application” = “RGMQL”
Queries
GMQL is not a traditional query language: With “query” we intend a group of operations that together produce a result; in this sense GMQL queries are more similar to SQL scripts. GMQL programming consists of a series of select, union, project, difference (and so on …) commands.
Let us see a short example:
Find somatic mutations in exon regions. Consider mutation data samples of human breast cancer cases. For each sample, quantify the mutations in each exon and select the exons with at least one mutation. Return the list of samples ordered by the number of such exons.
# These statements define the paths to the folders "EXON" and "MUT" in the
# subdirectory "example" of the package "RGMQL"
exon_path <- system.file("example", "EXON", package = "RGMQL")
mut_path <- system.file("example", "MUT", package = "RGMQL")
# Read EXON folder as a GMQL dataset named "exon_ds" containing a single
# sample with exon regions, and MUT folder as a GMQL dataset named "mut_ds"
exon_ds <- read_gmql(exon_path)
mut_ds <- read_gmql(mut_path)
# Filter out mut_ds based on a metadata predicate to keep breast cancer
# mutations only
mut = filter(mut_ds, manually_curated__dataType == 'dnaseq' &
clinical_patient__tumor_tissue_site == 'breast')
# Filter out exon_ds based on a metadata predicate to keep Refseq exons only
exon = filter(exon_ds, annotation_type == 'exons' &
original_provider == 'RefSeq')
# For each mutation sample, map the mutations to the exon regions using
# the map() function and count mutations within each exon storing the value
# in the default region attribute 'count_left_right'
exon1 <- map(exon, mut)
# Remove exons in each sample that do not contain mutations
exon2 <- filter(exon1, r_predicate = count_left_right >= 1)
# Using the extend() function, count how many exons remain in each sample and
# store the result in the sample metadata as a new attribute-value pair,
# with exon_count as attribute name
exon3 <- extend(exon2, exon_count = COUNT())
# Order samples in descending order of the added metadata exon_count
exon_res = arrange(exon3, list(DESC("exon_count")))If you want to store persistently the result, you can materialize it into a specific path defined as input parameter.
# Materialize the result dataset on disk
collect(exon_res)By default collect() has R working directory as storing path and ds1 as name of resulted dataset folder. Alternatively, we can specificy a different storing path and folder name as follows.+
# Materialize the result dataset into a specific folder on disk
collect(exon_res, dir_out = "./WD_R", name = "dataset") #, ## Warning in dir.create(res_dir_out): cannot create dir './WD_R/dataset', reason
## 'No such file or directory'Execution
RGMQL processing does not generate results until you invoke the execute() function.
execute()execute() can be issued only if at least one read() and at least one collect() are present in the RGMQL query, otherwise an error is generated. Data are saved in the path specified in every collect() present in the query. After the execution, the context of scalable data management engine is stopped and a new invocation of init_gmql() is needed.
Alternatively to or before execute() we can use:
g <- take(exon_res, rows = 45)to execute all the RGMQL coomands and extract data as GRangesList format in main memory. Specifically a GRangesList for each dataset and a GRanges for each sample is obtained.
NOTE: take() function works in local processing only and does not require a previous collect() function. Yet, GRangesList are contained in the R environment and are not saved on disk: collect() and execute() functions are needed to save data in mass memory
With the rows parameter it is possible to specify how many rows, for each sample inside the input dataset, are extracted; by default, the rows parameter value is \(0\), that means all rows are extracted. Note that, when dealing with big data, extracting all rows could be time demanding and very space consuming in main memory.
Remote Processing
RGMQL remote processing consumes computational power from remote cluster/system while managing GMQL datasets.
Remote processing exists in two flavour:
REST web services: User can write GMQL queries (using original GMQL syntax) to be executed remotely on remote data (or local data previously uploaded).
Sequential execution: Similar to local execution; user reads data and the system automatically uploads them on the remote system if they are not already there; once loaded, RGMQL functions can be issued to manage and process remote data.
REST Web Services
This RGMQL package allows invoking REST services that implement the commands specified at link.
Initialization
GMQL REST services require login; so, the first step is to perform login with user and password, or as guest. Upon successful logon, you get a request token that you must use in every subsequent REST call. Login can be performed using the login_gmql() function as a guest:
test_url = "http://www.gmql.eu/gmql-rest"
login_gmql(test_url)## [1] "your Token is c0f76649-2ba8-434d-8155-f541f6399252"Alternatively, login can be performed specifying previously defined user name and password, as to access each time the same private space on the GMQL remote repository. To create a new user registration, it is enough to use register_gmql(), specyfing all the needed parameters.
test_url = "http://www.gmql.eu/gmql-rest"
login_gmql(test_url, username = 'myname', password = 'mypassword')## [1] "Login still valid"Login saves a token in the Global R environment within the variable named authToken. With this token you can call all the functions in the GMQL REST Web services suite.
Execution
User can write a GMQL query as in the following example, and run it as second parameter of the run_query() function:
job <- run_query(test_url, "query_1", "DNA = SELECT() Example_Dataset_1;
MATERIALIZE DNA INTO RESULT_DS;", output_gtf = FALSE)Or the user can execute a query reading it directly from file (e.g., the “query1.txt” file in the “example” subdirectory of the RGMQL package):
query_path <- system.file("example", "query1.txt", package = "RGMQL")
job <- run_query_fromfile(test_url, query_path, output_gtf = FALSE)Once run, query continues on the remote server while run_query() or run_query_fromfile() returns immediately. User can extract from result (job) the job_id and status. jod_id can then be used to continuously invoke log and trace calls, both in this RGMQL package, to check for job completed status.
job_id <- job$id
trace_job(test_url, job_id)Then, results materialized on the remote repository can be downloaded locally and imported in GRangesList using the functions in this RGMQL package (see Import/Export).
The returned job contains also the name of the created datasets, one for each materialize in the GMQL query run, in the same order; the first can be downloaded locally with:
name_dataset <- job$datasets[[1]]$name
download_dataset(test_url, name_dataset)By default download_dataset() has R working directory as local storing path.
Downloaded result dataset can be then imported and used in the R environment as GRangesList (see Import/Export). Alternatively, the remote result dataset can be directly downloaded and imported in the R environment as GRangesList using the function download_as_GRangesList():
name_dataset <- job$datasets[[1]]$name
grl = download_as_GRangesList(test_url, name_dataset)Once download is done, we can logout from remote repository using:
logout_gmql(test_url)## [1] "Logout"logout_gmql() deletes the \(authToken\) from R environment.
Sequential Execution
This execution type is similar to local processing (syntax, functions, and so on …) except that materialized data are stored only on the remote repository, from where they can be downloaded locally and imported in GRangesList using the functions in this RGMQL package (see Import/Export).
Before starting with an example, note that we have to log into remote infrastructure with login_gmql() function:
test_url = "http://www.gmql.eu/gmql-rest"
login_gmql(test_url)Otherwise, we can initialize the data engine with a remote url:
init_gmql(url = test_url)## [1] "your Token is 5c419d52-ffde-4a7c-b074-e91b4a7f539d"In this way login is automatically performed as specified above while, by default, remote processing mode is set to FALSE. Thus, to proceed with query outsourcing we have to change to remote processing after initialization:
remote_processing(TRUE)## [1] "Remote processing On"Alternatively, instead of switching mode, we can initialize the data engine by setting remote processing as TRUE, in the corresponding init_gmql parameter:
init_gmql(url = test_url, remote_processing = TRUE)Once done, we can start building the query that will be processed remotely:
## Read the remote dataset HG19_TCGA_dnaseq
## Read the remote dataset HG19_BED_ANNOTATION
TCGA_dnaseq <- read_gmql("public.HG19_TCGA_dnaseq", is_local = FALSE)
HG19_bed_ann <- read_gmql("public.HG19_BED_ANNOTATION", is_local = FALSE)
# Filter out mut_ds based on a metadata predicate to keep breast cancer
# mutations only
mut = filter(TCGA_dnaseq, manually_curated__dataType == 'dnaseq' &
clinical_patient__tumor_tissue_site == 'breast')
# Filter out exon_ds based on a metadata predicate to keep Refseq exons only
exon = filter(HG19_bed_ann, annotation_type == 'exons' &
original_provider == 'RefSeq')
# For each mutation sample, map the mutations to the exon regions using
# the map() function and count mutations within each exon storing the value
# in the default region attribute 'count_left_right'
exon1 <- map(exon, mut)
# Remove exons in each sample that do not contain mutations
exon2 <- filter(exon1, r_predicate = count_left_right >= 1)
# Using the extend() function, count how many exons remain in each sample and
# store the result in the sample metadata as a new attribute-value pair,
# with exon_count as attribute name
exon3 <- extend(exon2, exon_count = COUNT())
# Order samples in descending order of the added metadata exon_count
exon_res = arrange(exon3, list(DESC("exon_count")))N.B. In case of remote processing, for collect() function we have to specify the name of the output dataset (not necessarily the same as input) as the second parameter in order to correctly process the query on the remote GMQL system. Here it is the needed R code:
collect(exon_res, name="exon_res_data")job<-execute()In this case R processing continues until the remote processing ends. With remote processing, after the execution, the context of the scalable data management engine is not stopped, and can be used for further queries. Materialized datasets are stored only remotely, from where they can be downloaded and stored on local disk:
name_dataset <- job$datasets[[1]]$name
download_dataset(test_url, name_dataset)and/or directly imported into the R environment as GRangesList using the function download_as_GRangesList():
name_dataset <- job$datasets[[1]]$name
grl = download_as_GRangesList(test_url, name_dataset)Additionally, any dataset previously downloaded and stored locally can be then imported in the R environment as GRangesList (see Import/Export).
In any case, once download is done, we can logout from remote repository using:
logout_gmql(test_url)Mixed Processing
As said before, the processing mode can be switched using the function:
test_url = "http://www.gmql.eu/gmql-rest"
init_gmql(url = test_url)
remote_processing(TRUE)## [1] "Remote processing On"An user can switch processing mode until the first collect() has been performed.
This kind of processing comes from the fact that the read_gmql() function can accept either a local dataset or a remote repository dataset, even in the same query as in the following example:
# This statement defines the path to the folder "MUT" in the subdirectory
# "example" of the package "RGMQL"
mut_path <- system.file("example", "MUT", package = "RGMQL")
# Read MUT folder as a GMQL dataset named "mut_ds"
mut_ds <- read_gmql(mut_path, is_local = TRUE)
# Read the remote dataset HG19_BED_ANNOTATION
HG19_bed_ann <- read_gmql("public.HG19_BED_ANNOTATION", is_local = FALSE)
# Filter out mut_ds based on a metadata predicate to keep breast cancer
# mutations only
mut = filter(mut_ds, manually_curated__dataType == 'dnaseq' &
clinical_patient__tumor_tissue_site == 'breast')
# Filter out exon_ds based on a metadata predicate to keep Refseq exons only
exon = filter(HG19_bed_ann, annotation_type == 'exons' &
original_provider == 'RefSeq')
# For each mutation sample, map the mutations to the exon regions using
# the map() function and count mutations within each exon storing the value
# in the default region attribute 'count_left_right'
exon1 <- map(exon, mut)
# Remove exons in each sample that do not contain mutations
exon2 <- filter(exon1, r_predicate = count_left_right >= 1)
# Using the extend() function, count how many exons remain in each sample and
# store the result in the sample metadata as a new attribute-value pair,
# with exon_count as attribute name
exon3 <- extend(exon2, exon_count = COUNT())
# Order samples in descending order of the added metadata exon_count
exon_res = arrange(exon3, list(DESC("exon_count")))Materialize result:
collect(exon_res,"exon_result_dataset")Execute processing:
job<-execute()As we can see, the two read_gmql() functions above read from different sources: mut_ds from local dataset, HG19_BED_ANNOTATION from remote repository.
If we set remote processing to false (remote_processing(FALSE)), the execution is performed locally downloading first all needed datasets from the GMQL remote repository; otherwise, all local datasets are automatically uploaded to the remote GMQL repository associated with the remote system where the processing is performed. In this latter case, materialized datasets are stored on the remote repository, from where they can be downloaded and imported into the R environment like in the two previous remote processing scenarios (see Remote Processing).
NOTE: The public datasets cannot be downloaded entirely from the remote GMQL repository by design.
Utilities
The RGMQL package contains functions that allow the user to interface with other packages available in R/Bioconductor repository, e.g., GenomicRanges, cBioPortalData, TFHAZ, TFARM. Some of RGQML functions are developed to directly provide extensibility over core data structures and processing functions commonly used in the R/Bioconductor environment, such as most of the manipulation functions provided by dyplr package. Some other functions can return or read GRangesList or GRanges objects with associated metadata (if present), and such data structures are suitable to further processing by a variety of other R/Bioconductor packages.
Import/Export
We can import a GMQL dataset into R environment as follows:
# This statement defines the path to the folder "EXON" in the subdirectory
# "example" of the package "RGMQL"
dataset_path <- system.file("example", "EXON", package = "RGMQL")
# Import the GMQL dataset EXON as GRangesList
imported_data <- import_gmql(dataset_path, is_gtf = FALSE)
imported_data## GRangesList object of length 1:
## $S_00000
## GRanges object with 571 ranges and 2 metadata columns:
## seqnames ranges strand | name score
## <Rle> <IRanges> <Rle> | <character> <integer>
## [1] chr1 11874-12227 + | NR_046018 0
## [2] chr1 12613-12721 + | NR_046018 0
## [3] chr1 917445-917497 - | NM_001291366 0
## [4] chr1 934342-934812 - | NM_021170 0
## [5] chr1 934344-934812 - | NM_001142467 0
## ... ... ... ... . ... ...
## [567] chr7 128612480-128612636 - | NR_034053 0
## [568] chr7 128612480-128612636 - | NM_001191028 0
## [569] chr7 128612480-128612636 - | NM_012470 0
## [570] chr7 128614922-128615016 - | NR_034053 0
## [571] chr7 128614922-128615016 - | NM_001191028 0
## -------
## seqinfo: 11 sequences from an unspecified genome; no seqlengths# and its metadata
imported_data@metadata## $S_00000
## $S_00000$annotation_type
## [1] "exons"
##
## $S_00000$assembly
## [1] "hg19"
##
## $S_00000$name
## [1] "RefSeqGeneExons"
##
## $S_00000$original_provider
## [1] "RefSeq"
##
## $S_00000$provider
## [1] "POLIMI"The second parameter is_gtf must specify the file format: .GTF or .GDM.
We can export a GRangesList as a GMQL dataset as follows:
# This statement defines the path to the subdirectory "exp" of the
# package "RGMQL"
dir_out <- paste(system.file("example", package = "RGMQL"), 'exp', sep='/')
# Export the GRangesList 'imported_data' as GMQL dataset called 'example'
# at destination path
export_gmql(imported_data, dir_out, is_gtf = TRUE)## The following `from` values were not present in `x`: type, phase## [1] "Export to GTF complete"The second parameter is_gtf must specify the file format: .GTF or .GDM.
Filter and Extract
We can also import only a part of a GMQL dataset into R environment, by filtering its content based on metadata and/or region attributes. Following, we extract from a gene expression dataset of adrenocortical carcinoma patients all the sample profiles, but focusing only on the raw count expression values.
# This statement defines the path to the folder "TCGA-ACC" in the subdirectory
# "example" of the package "RGMQL"
data_in <- system.file("example", "TCGA-ACC", package = "RGMQL")
matrix <- filter_and_extract(data_in, metadata= NULL,
region_attributes =
FULL(except = c('fpkm_uq','fpkm')))## New names:
## New names:
## • `ensembl_gene_id` -> `ensembl_gene_id...1`
## • `entrez_gene_id` -> `entrez_gene_id...2`
## • `gene_symbol` -> `gene_symbol...3`
## • `type` -> `type...4`
## • `htseq_count` -> `htseq_count...5`
## • `ensembl_gene_id` -> `ensembl_gene_id...6`
## • `entrez_gene_id` -> `entrez_gene_id...7`
## • `gene_symbol` -> `gene_symbol...8`
## • `type` -> `type...9`
## • `htseq_count` -> `htseq_count...10`
## • `ensembl_gene_id` -> `ensembl_gene_id...11`
## • `entrez_gene_id` -> `entrez_gene_id...12`
## • `gene_symbol` -> `gene_symbol...13`
## • `type` -> `type...14`
## • `htseq_count` -> `htseq_count...15`
## • `ensembl_gene_id` -> `ensembl_gene_id...16`
## • `entrez_gene_id` -> `entrez_gene_id...17`
## • `gene_symbol` -> `gene_symbol...18`
## • `type` -> `type...19`
## • `htseq_count` -> `htseq_count...20`
## • `ensembl_gene_id` -> `ensembl_gene_id...21`
## • `entrez_gene_id` -> `entrez_gene_id...22`
## • `gene_symbol` -> `gene_symbol...23`
## • `type` -> `type...24`
## • `htseq_count` -> `htseq_count...25`
## • `ensembl_gene_id` -> `ensembl_gene_id...26`
## • `entrez_gene_id` -> `entrez_gene_id...27`
## • `gene_symbol` -> `gene_symbol...28`
## • `type` -> `type...29`
## • `htseq_count` -> `htseq_count...30`
## • `ensembl_gene_id` -> `ensembl_gene_id...31`
## • `entrez_gene_id` -> `entrez_gene_id...32`
## • `gene_symbol` -> `gene_symbol...33`
## • `type` -> `type...34`
## • `htseq_count` -> `htseq_count...35`
## • `ensembl_gene_id` -> `ensembl_gene_id...36`
## • `entrez_gene_id` -> `entrez_gene_id...37`
## • `gene_symbol` -> `gene_symbol...38`
## • `type` -> `type...39`
## • `htseq_count` -> `htseq_count...40`
## • `ensembl_gene_id` -> `ensembl_gene_id...41`
## • `entrez_gene_id` -> `entrez_gene_id...42`
## • `gene_symbol` -> `gene_symbol...43`
## • `type` -> `type...44`
## • `htseq_count` -> `htseq_count...45`
## • `ensembl_gene_id` -> `ensembl_gene_id...46`
## • `entrez_gene_id` -> `entrez_gene_id...47`
## • `gene_symbol` -> `gene_symbol...48`
## • `type` -> `type...49`
## • `htseq_count` -> `htseq_count...50`
## • `ensembl_gene_id` -> `ensembl_gene_id...51`
## • `entrez_gene_id` -> `entrez_gene_id...52`
## • `gene_symbol` -> `gene_symbol...53`
## • `type` -> `type...54`
## • `htseq_count` -> `htseq_count...55`
## • `ensembl_gene_id` -> `ensembl_gene_id...56`
## • `entrez_gene_id` -> `entrez_gene_id...57`
## • `gene_symbol` -> `gene_symbol...58`
## • `type` -> `type...59`
## • `htseq_count` -> `htseq_count...60`
## • `ensembl_gene_id` -> `ensembl_gene_id...61`
## • `entrez_gene_id` -> `entrez_gene_id...62`
## • `gene_symbol` -> `gene_symbol...63`
## • `type` -> `type...64`
## • `htseq_count` -> `htseq_count...65`
## • `ensembl_gene_id` -> `ensembl_gene_id...66`
## • `entrez_gene_id` -> `entrez_gene_id...67`
## • `gene_symbol` -> `gene_symbol...68`
## • `type` -> `type...69`
## • `htseq_count` -> `htseq_count...70`
## • `ensembl_gene_id` -> `ensembl_gene_id...71`
## • `entrez_gene_id` -> `entrez_gene_id...72`
## • `gene_symbol` -> `gene_symbol...73`
## • `type` -> `type...74`
## • `htseq_count` -> `htseq_count...75`matrix## GRanges object with 60483 ranges and 75 metadata columns:
## seqnames ranges strand | ensembl_gene_id....
## <Rle> <IRanges> <Rle> | <character>
## [1] chr1 11868-14409 + | ENSG00000223972.5
## [2] chr1 14403-29570 - | ENSG00000227232.5
## [3] chr1 17368-17436 - | ENSG00000278267.1
## [4] chr1 29553-31109 + | ENSG00000243485.3
## [5] chr1 30365-30503 + | ENSG00000274890.1
## ... ... ... ... . ...
## [60479] chrY 57190737-57208756 + | ENSGR0000270726.4
## [60480] chrY 57201142-57203357 - | ENSGR0000185203.10
## [60481] chrY 57207345-57212230 + | ENSGR0000182484.13
## [60482] chrY 57209150-57209218 + | ENSGR0000276543.3
## [60483] chrY 57212183-57214397 - | ENSGR0000227159.6
## entrez_gene_id.... gene_symbol.... type.... htseq_count....
## <integer> <character> <character> <integer>
## [1] 100287102 DDX11L1 gene 0
## [2] 653635 WASH7P gene 95
## [3] 102465910 MIR6859-3 gene 0
## [4] <NA> RP11-34P13.3 gene 0
## [5] 100422831 MIR1302-9 gene 0
## ... ... ... ... ...
## [60479] <NA> AJ271736.10 gene 0
## [60480] 100128260 WASIR1 gene 0
## [60481] 653440 WASH6P gene 0
## [60482] <NA> AJ271736.1 gene 0
## [60483] 727856 DDX11L16 gene 0
## ensembl_gene_id.....1 entrez_gene_id.....1 gene_symbol.....1
## <character> <integer> <character>
## [1] ENSG00000223972.5 100287102 DDX11L1
## [2] ENSG00000227232.5 653635 WASH7P
## [3] ENSG00000278267.1 102465910 MIR6859-3
## [4] ENSG00000243485.3 <NA> RP11-34P13.3
## [5] ENSG00000274890.1 100422831 MIR1302-9
## ... ... ... ...
## [60479] ENSGR0000270726.4 <NA> AJ271736.10
## [60480] ENSGR0000185203.10 100128260 WASIR1
## [60481] ENSGR0000182484.13 653440 WASH6P
## [60482] ENSGR0000276543.3 <NA> AJ271736.1
## [60483] ENSGR0000227159.6 727856 DDX11L16
## type.....1 htseq_count.....1 ensembl_gene_id.....2
## <character> <integer> <character>
## [1] gene 0 ENSG00000223972.5
## [2] gene 61 ENSG00000227232.5
## [3] gene 0 ENSG00000278267.1
## [4] gene 0 ENSG00000243485.3
## [5] gene 0 ENSG00000274890.1
## ... ... ... ...
## [60479] gene 0 ENSGR0000270726.4
## [60480] gene 0 ENSGR0000185203.10
## [60481] gene 0 ENSGR0000182484.13
## [60482] gene 0 ENSGR0000276543.3
## [60483] gene 0 ENSGR0000227159.6
## entrez_gene_id.....2 gene_symbol.....2 type.....2 htseq_count.....2
## <integer> <character> <character> <integer>
## [1] 100287102 DDX11L1 gene 0
## [2] 653635 WASH7P gene 48
## [3] 102465910 MIR6859-3 gene 0
## [4] <NA> RP11-34P13.3 gene 0
## [5] 100422831 MIR1302-9 gene 0
## ... ... ... ... ...
## [60479] <NA> AJ271736.10 gene 0
## [60480] 100128260 WASIR1 gene 0
## [60481] 653440 WASH6P gene 0
## [60482] <NA> AJ271736.1 gene 0
## [60483] 727856 DDX11L16 gene 0
## ensembl_gene_id.....3 entrez_gene_id.....3 gene_symbol.....3
## <character> <integer> <character>
## [1] ENSG00000223972.5 100287102 DDX11L1
## [2] ENSG00000227232.5 653635 WASH7P
## [3] ENSG00000278267.1 102465910 MIR6859-3
## [4] ENSG00000243485.3 <NA> RP11-34P13.3
## [5] ENSG00000274890.1 100422831 MIR1302-9
## ... ... ... ...
## [60479] ENSGR0000270726.4 <NA> AJ271736.10
## [60480] ENSGR0000185203.10 100128260 WASIR1
## [60481] ENSGR0000182484.13 653440 WASH6P
## [60482] ENSGR0000276543.3 <NA> AJ271736.1
## [60483] ENSGR0000227159.6 727856 DDX11L16
## type.....3 htseq_count.....3 ensembl_gene_id.....4
## <character> <integer> <character>
## [1] gene 0 ENSG00000223972.5
## [2] gene 49 ENSG00000227232.5
## [3] gene 0 ENSG00000278267.1
## [4] gene 0 ENSG00000243485.3
## [5] gene 0 ENSG00000274890.1
## ... ... ... ...
## [60479] gene 0 ENSGR0000270726.4
## [60480] gene 0 ENSGR0000185203.10
## [60481] gene 0 ENSGR0000182484.13
## [60482] gene 0 ENSGR0000276543.3
## [60483] gene 0 ENSGR0000227159.6
## entrez_gene_id.....4 gene_symbol.....4 type.....4 htseq_count.....4
## <integer> <character> <character> <integer>
## [1] 100287102 DDX11L1 gene 0
## [2] 653635 WASH7P gene 33
## [3] 102465910 MIR6859-3 gene 0
## [4] <NA> RP11-34P13.3 gene 0
## [5] 100422831 MIR1302-9 gene 0
## ... ... ... ... ...
## [60479] <NA> AJ271736.10 gene 0
## [60480] 100128260 WASIR1 gene 0
## [60481] 653440 WASH6P gene 0
## [60482] <NA> AJ271736.1 gene 0
## [60483] 727856 DDX11L16 gene 0
## ensembl_gene_id.....5 entrez_gene_id.....5 gene_symbol.....5
## <character> <integer> <character>
## [1] ENSG00000223972.5 100287102 DDX11L1
## [2] ENSG00000227232.5 653635 WASH7P
## [3] ENSG00000278267.1 102465910 MIR6859-3
## [4] ENSG00000243485.3 <NA> RP11-34P13.3
## [5] ENSG00000274890.1 100422831 MIR1302-9
## ... ... ... ...
## [60479] ENSGR0000270726.4 <NA> AJ271736.10
## [60480] ENSGR0000185203.10 100128260 WASIR1
## [60481] ENSGR0000182484.13 653440 WASH6P
## [60482] ENSGR0000276543.3 <NA> AJ271736.1
## [60483] ENSGR0000227159.6 727856 DDX11L16
## type.....5 htseq_count.....5 ensembl_gene_id.....6
## <character> <integer> <character>
## [1] gene 0 ENSG00000223972.5
## [2] gene 56 ENSG00000227232.5
## [3] gene 0 ENSG00000278267.1
## [4] gene 0 ENSG00000243485.3
## [5] gene 0 ENSG00000274890.1
## ... ... ... ...
## [60479] gene 0 ENSGR0000270726.4
## [60480] gene 0 ENSGR0000185203.10
## [60481] gene 0 ENSGR0000182484.13
## [60482] gene 0 ENSGR0000276543.3
## [60483] gene 0 ENSGR0000227159.6
## entrez_gene_id.....6 gene_symbol.....6 type.....6 htseq_count.....6
## <integer> <character> <character> <integer>
## [1] 100287102 DDX11L1 gene 0
## [2] 653635 WASH7P gene 49
## [3] 102465910 MIR6859-3 gene 0
## [4] <NA> RP11-34P13.3 gene 0
## [5] 100422831 MIR1302-9 gene 0
## ... ... ... ... ...
## [60479] <NA> AJ271736.10 gene 0
## [60480] 100128260 WASIR1 gene 0
## [60481] 653440 WASH6P gene 0
## [60482] <NA> AJ271736.1 gene 0
## [60483] 727856 DDX11L16 gene 0
## ensembl_gene_id.....7 entrez_gene_id.....7 gene_symbol.....7
## <character> <integer> <character>
## [1] ENSG00000223972.5 100287102 DDX11L1
## [2] ENSG00000227232.5 653635 WASH7P
## [3] ENSG00000278267.1 102465910 MIR6859-3
## [4] ENSG00000243485.3 <NA> RP11-34P13.3
## [5] ENSG00000274890.1 100422831 MIR1302-9
## ... ... ... ...
## [60479] ENSGR0000270726.4 <NA> AJ271736.10
## [60480] ENSGR0000185203.10 100128260 WASIR1
## [60481] ENSGR0000182484.13 653440 WASH6P
## [60482] ENSGR0000276543.3 <NA> AJ271736.1
## [60483] ENSGR0000227159.6 727856 DDX11L16
## type.....7 htseq_count.....7 ensembl_gene_id.....8
## <character> <integer> <character>
## [1] gene 0 ENSG00000223972.5
## [2] gene 43 ENSG00000227232.5
## [3] gene 1 ENSG00000278267.1
## [4] gene 0 ENSG00000243485.3
## [5] gene 0 ENSG00000274890.1
## ... ... ... ...
## [60479] gene 0 ENSGR0000270726.4
## [60480] gene 0 ENSGR0000185203.10
## [60481] gene 0 ENSGR0000182484.13
## [60482] gene 0 ENSGR0000276543.3
## [60483] gene 0 ENSGR0000227159.6
## entrez_gene_id.....8 gene_symbol.....8 type.....8 htseq_count.....8
## <integer> <character> <character> <integer>
## [1] 100287102 DDX11L1 gene 0
## [2] 653635 WASH7P gene 25
## [3] 102465910 MIR6859-3 gene 0
## [4] <NA> RP11-34P13.3 gene 0
## [5] 100422831 MIR1302-9 gene 0
## ... ... ... ... ...
## [60479] <NA> AJ271736.10 gene 0
## [60480] 100128260 WASIR1 gene 0
## [60481] 653440 WASH6P gene 0
## [60482] <NA> AJ271736.1 gene 0
## [60483] 727856 DDX11L16 gene 0
## ensembl_gene_id.....9 entrez_gene_id.....9 gene_symbol.....9
## <character> <integer> <character>
## [1] ENSG00000223972.5 100287102 DDX11L1
## [2] ENSG00000227232.5 653635 WASH7P
## [3] ENSG00000278267.1 102465910 MIR6859-3
## [4] ENSG00000243485.3 <NA> RP11-34P13.3
## [5] ENSG00000274890.1 100422831 MIR1302-9
## ... ... ... ...
## [60479] ENSGR0000270726.4 <NA> AJ271736.10
## [60480] ENSGR0000185203.10 100128260 WASIR1
## [60481] ENSGR0000182484.13 653440 WASH6P
## [60482] ENSGR0000276543.3 <NA> AJ271736.1
## [60483] ENSGR0000227159.6 727856 DDX11L16
## type.....9 htseq_count.....9 ensembl_gene_id.....10
## <character> <integer> <character>
## [1] gene 0 ENSG00000223972.5
## [2] gene 55 ENSG00000227232.5
## [3] gene 1 ENSG00000278267.1
## [4] gene 0 ENSG00000243485.3
## [5] gene 0 ENSG00000274890.1
## ... ... ... ...
## [60479] gene 0 ENSGR0000270726.4
## [60480] gene 0 ENSGR0000185203.10
## [60481] gene 0 ENSGR0000182484.13
## [60482] gene 0 ENSGR0000276543.3
## [60483] gene 0 ENSGR0000227159.6
## entrez_gene_id.....10 gene_symbol.....10 type.....10
## <integer> <character> <character>
## [1] 100287102 DDX11L1 gene
## [2] 653635 WASH7P gene
## [3] 102465910 MIR6859-3 gene
## [4] <NA> RP11-34P13.3 gene
## [5] 100422831 MIR1302-9 gene
## ... ... ... ...
## [60479] <NA> AJ271736.10 gene
## [60480] 100128260 WASIR1 gene
## [60481] 653440 WASH6P gene
## [60482] <NA> AJ271736.1 gene
## [60483] 727856 DDX11L16 gene
## htseq_count.....10 ensembl_gene_id.....11 entrez_gene_id.....11
## <integer> <character> <integer>
## [1] 0 ENSG00000223972.5 100287102
## [2] 81 ENSG00000227232.5 653635
## [3] 1 ENSG00000278267.1 102465910
## [4] 0 ENSG00000243485.3 <NA>
## [5] 0 ENSG00000274890.1 100422831
## ... ... ... ...
## [60479] 0 ENSGR0000270726.4 <NA>
## [60480] 0 ENSGR0000185203.10 100128260
## [60481] 0 ENSGR0000182484.13 653440
## [60482] 0 ENSGR0000276543.3 <NA>
## [60483] 0 ENSGR0000227159.6 727856
## gene_symbol.....11 type.....11 htseq_count.....11
## <character> <character> <integer>
## [1] DDX11L1 gene 0
## [2] WASH7P gene 22
## [3] MIR6859-3 gene 0
## [4] RP11-34P13.3 gene 0
## [5] MIR1302-9 gene 0
## ... ... ... ...
## [60479] AJ271736.10 gene 0
## [60480] WASIR1 gene 0
## [60481] WASH6P gene 0
## [60482] AJ271736.1 gene 0
## [60483] DDX11L16 gene 0
## ensembl_gene_id.....12 entrez_gene_id.....12 gene_symbol.....12
## <character> <integer> <character>
## [1] ENSG00000223972.5 100287102 DDX11L1
## [2] ENSG00000227232.5 653635 WASH7P
## [3] ENSG00000278267.1 102465910 MIR6859-3
## [4] ENSG00000243485.3 <NA> RP11-34P13.3
## [5] ENSG00000274890.1 100422831 MIR1302-9
## ... ... ... ...
## [60479] ENSGR0000270726.4 <NA> AJ271736.10
## [60480] ENSGR0000185203.10 100128260 WASIR1
## [60481] ENSGR0000182484.13 653440 WASH6P
## [60482] ENSGR0000276543.3 <NA> AJ271736.1
## [60483] ENSGR0000227159.6 727856 DDX11L16
## type.....12 htseq_count.....12 ensembl_gene_id.....13
## <character> <integer> <character>
## [1] gene 0 ENSG00000223972.5
## [2] gene 63 ENSG00000227232.5
## [3] gene 1 ENSG00000278267.1
## [4] gene 0 ENSG00000243485.3
## [5] gene 0 ENSG00000274890.1
## ... ... ... ...
## [60479] gene 0 ENSGR0000270726.4
## [60480] gene 0 ENSGR0000185203.10
## [60481] gene 0 ENSGR0000182484.13
## [60482] gene 0 ENSGR0000276543.3
## [60483] gene 0 ENSGR0000227159.6
## entrez_gene_id.....13 gene_symbol.....13 type.....13
## <integer> <character> <character>
## [1] 100287102 DDX11L1 gene
## [2] 653635 WASH7P gene
## [3] 102465910 MIR6859-3 gene
## [4] <NA> RP11-34P13.3 gene
## [5] 100422831 MIR1302-9 gene
## ... ... ... ...
## [60479] <NA> AJ271736.10 gene
## [60480] 100128260 WASIR1 gene
## [60481] 653440 WASH6P gene
## [60482] <NA> AJ271736.1 gene
## [60483] 727856 DDX11L16 gene
## htseq_count.....13 ensembl_gene_id.....14 entrez_gene_id.....14
## <integer> <character> <integer>
## [1] 2 ENSG00000223972.5 100287102
## [2] 11 ENSG00000227232.5 653635
## [3] 0 ENSG00000278267.1 102465910
## [4] 0 ENSG00000243485.3 <NA>
## [5] 0 ENSG00000274890.1 100422831
## ... ... ... ...
## [60479] 0 ENSGR0000270726.4 <NA>
## [60480] 0 ENSGR0000185203.10 100128260
## [60481] 0 ENSGR0000182484.13 653440
## [60482] 0 ENSGR0000276543.3 <NA>
## [60483] 0 ENSGR0000227159.6 727856
## gene_symbol.....14 type.....14 htseq_count.....14
## <character> <character> <integer>
## [1] DDX11L1 gene 0
## [2] WASH7P gene 107
## [3] MIR6859-3 gene 0
## [4] RP11-34P13.3 gene 0
## [5] MIR1302-9 gene 0
## ... ... ... ...
## [60479] AJ271736.10 gene 0
## [60480] WASIR1 gene 0
## [60481] WASH6P gene 0
## [60482] AJ271736.1 gene 0
## [60483] DDX11L16 gene 0
## -------
## seqinfo: 25 sequences from an unspecified genome; no seqlengthsfilter_and_extract() filters the samples in the input dataset based on the specified metadata attributes of interest and then, for each filtered sample, extracts the GRanges coordinate attributes (seqnames, start, stop, strand) together with other region_attributes specified to be retrieved and kept from the input dataset (possibly all if \(region\_attributes\) = FULL(except = NULL)). If the \(metadata\) argument is NULL, all samples are taken without filtering. If \(region\_attributes\) is not specified, only the fundamental elements of GRanges are extracted, i.e., the genomic coordinates.
Any additional region attribute from \(region\_attributes\) is a metadata column of the GRanges obtained for each filtered sample. The total number of obtained columns is equal to the number of samples left after filtering, multiplied by the number of specified region attributes.
NOTE: filter_and_extract() works only if every sample in the dataset includes the same number of regions with the same coordinates.
Each metadata column is named using region_attributes concatenated with the function input parameter suffix. By default suffix correspond to a metadata: antibody_target.
Metadata
Each sample of a GMQL dataset has its own metadata associated and generally every metadata attribute has a single value. An example of distinct values for the same metadata attribute is shown in the figure below for the metadata attribute. We suppose that more than one disease is associated to each sample, for which annotations to indicate over-expressed genes are provided.
In this case GMQL automatically handles this situation. In the Import/export paragraph, we showed that a GMQL dataset can be imported into R environment as a GRangesList, together with its metadata.
# This statement defines the path to the folder "DATASET_META" in the
# subdirectory "example" of the package "RGMQL"
dataset_path <- system.file("example", "DATASET_META", package = "RGMQL")
# Import the GMQL dataset DATASET_META as GRangesList
grl_data <- import_gmql(dataset_path, is_gtf = FALSE)
grl_data## GRangesList object of length 1:
## $S_00000
## GRanges object with 571 ranges and 2 metadata columns:
## seqnames ranges strand | name overexpression_score
## <Rle> <IRanges> <Rle> | <character> <integer>
## [1] chr1 11874-12227 + | NR_046018 0
## [2] chr1 12613-12721 + | NR_046018 0
## [3] chr1 917445-917497 - | NM_001291366 0
## [4] chr1 934342-934812 - | NM_021170 0
## [5] chr1 934344-934812 - | NM_001142467 0
## ... ... ... ... . ... ...
## [567] chr7 128612480-128612636 - | NR_034053 0
## [568] chr7 128612480-128612636 - | NM_001191028 0
## [569] chr7 128612480-128612636 - | NM_012470 0
## [570] chr7 128614922-128615016 - | NR_034053 0
## [571] chr7 128614922-128615016 - | NM_001191028 0
## -------
## seqinfo: 11 sequences from an unspecified genome; no seqlengths# and its metadata
grl_data@metadata## $S_00000
## $S_00000$sample_id
## [1] "" "000112"
##
## $S_00000$assembly
## [1] "" "hg19"
##
## $S_00000$disease
## [1] "" "" "cancer"
##
## $S_00000$disease
## [1] "" "" "pulmonary fibrosis"
##
## $S_00000$disease
## [1] "" "" "Tuberous sclerosis"
##
## $S_00000$disease
## [1] "" ""
## [3] "neurofibromatosis type 1"
##
## $S_00000$name
## [1] "" ""
## [3] "over-expressed gene annotations"
##
## $S_00000$original_provider
## [1] "Memorial Hospital"
##
## $S_00000$provider
## [1] "" "POLIMI"The metadata are stored as simple list in the form key-values and it does not matter if mutiple values for the same metadata attribute are present; all values are stored and shown. Difficulties can arise when we need to get all the metadata values; normally, since the metadata list is in the form key-value, we can extract the metadata values using:
# store metadata on variable a
a = grl_data@metadata
# get disease value of sample S_00000
a$S_00000$disease## [1] "" "" "cancer"Yet, in this case only the first disease value is shown. If we want to retrieve all disease values, we should use instead:
# get all disease values of sample S_00000
a$S_00000[which(names(a$S_00000) %in% "disease")]## $disease
## [1] "" "" "cancer"
##
## $disease
## [1] "" "" "pulmonary fibrosis"
##
## $disease
## [1] "" "" "Tuberous sclerosis"
##
## $disease
## [1] "" ""
## [3] "neurofibromatosis type 1"Windows OS Issues
Be aware that during a local processing execution an error message
Error in .jcall("RJavaTools", "Ljava/lang/Object;", "invokeMethod", cl,
: org.apache.spark.SparkException: Job aborted due to stage failure:
Task 0 in stage 7.0 failed 1 times, most recent failure:
Lost task 0.0 in stage 7.0 (TID 59, localhost, executor driver):
java.io.IOException: (null) entry in command string: null chmod 0644 may arise.
This happens because some Hadoop binary files are missing in Windows 64Bits. In this case we need to:
- Go to https://github.com/steveloughran/winutils, download the repository
- Create a directory ‘hadoop’ with a sub-directory ‘bin’ in a path of your choice (for example at
C:\Program Files\hadoop\bin). - Copy the files from the repository folder hadoop-2.8.1 into the ‘bin’ sub-directory earlier created.
- Create an environment variable HADOOP_HOME with value equals to the path reaching the ‘bin’ directory where you just copied the files.
References
1. Masseroli M, Pinoli P, Venco F, Kaitoua A, Jalili V, Paluzzi F, Muller H, Ceri S. GenoMetric Query Language: A novel approach to large-scale genomic data management. Bioinformatics. 2015;31(12):1881-1888.
2. Ceri S, Kaitoua A, Masseroli M, Pinoli P, Venco F. Data management for heterogeneous genomic datasets. IEEE/ACM Trans Comput Biol Bioinform. 2017;14(6):1251-1264.
3. GenoMetric Query Language open source software on GitHub repository. Published online 2017. https://github.com/DEIB-GECO/GMQL/
4. Masseroli M, Kaitoua A, Pinoli P, Ceri S. Modeling and interoperability of heterogeneous genomic big data for integrative processing and querying. Methods. 2016;111:3-11.