View source: R/getCollection.R
getCollection | R Documentation |
Main collection retrieval function for an organism of interest. By specifying the scientific name of an organism of interest a collection consisting of the genome file, proteome file, CDS file, RNA file, GFF file, Repeat Masker file, AssemblyStats file of the organism of interest can be downloaded and stored locally. Collections can be retrieved from several databases. For full set of collection elements, see: biomartr:::supported_biotypes(db)
getCollection(
db = "refseq",
organism,
reference = TRUE,
skip_bacteria = TRUE,
release = NULL,
assembly_type = "toplevel",
analyse_genome = FALSE,
remove_annotation_outliers = FALSE,
gunzip = FALSE,
path = file.path("_db_downloads", "collections"),
mute_citation = FALSE
)
db |
a character string specifying the database from which the genome shall be retrieved:
|
organism |
Organism selector id, there are three options to characterize an organism:
|
reference |
a logical value indicating whether or not a genome shall be a candidate for downloaded if it isn't marked in the database as either a reference genome or a representative genome. This is helpful if you don't want to allow "partial genomes" etc. |
skip_bacteria |
Due to its enormous dataset size (> 700MB as of July 2023),
the bacterial summary file will not be loaded by default anymore. If users
wish to gain insights for the bacterial kingdom they needs to actively specify |
release |
a numeric, the database release version of ENSEMBL ( |
assembly_type |
character, default c("primary_assembly", "toplevel"). Used for ensembl only, specifies the genome assembly type. Searches for both primary and toplevel, and if both are found, uses the first by order (so primary is prioritized by default). The Primary assembly should usually be used if it exists. The "primary assembly" contains all the top-level sequence regions, excluding alternative haplotypes and patches. If the primary assembly file is not present for a species (only defined for standard model organisms), that indicates that there were no haplotype/patch regions, and in such cases, the 'toplevel file is used. For more details see: ensembl tutorial |
analyse_genome |
logical, default FALSE. If TRUE, get general genome statistics like gc content etc. For more details, see ?summary_genome |
remove_annotation_outliers |
shall outlier lines be removed from the input |
gunzip |
a logical, indicating whether or not files should be unzipped. |
path |
a character string specifying the location (a folder) in which
the corresponding collection shall be stored. Default is
|
mute_citation |
logical, default FALSE, indicating whether citation message should be muted. |
Fetching of assembly / sequence data is done by fetching an overview file
from metadata of given database:
For NCBI (refseq/genbank):
Internally this function loads the the overview.txt file from NCBI:
refseq: ftp.ncbi.nlm.nih.gov/genomes/refseq/
genbank: ftp.ncbi.nlm.nih.gov/genomes/genbank/
It will then create a directory relative to file type wanted,
if you get fasta genomes it will be
_ncbi_downloads/genomes' etc.
In case the corresponding fasta file already exists within the
'_ncbi_downloads/genomes' folder and is accessible within the workspace,
no download process will be performed.
For other file types the same rule applies.
For ensembl it fetches overview per type from the rest API:
ensembl: https://rest.ensembl.org
File path to downloaded genome.
Hajk-Georg Drost
Other getBio:
getBio()
,
getCDS()
,
getGFF()
,
getGenome()
,
getProteome()
,
getRNA()
Other collection:
getCollectionSet()
## Not run:
# download the collection of Homo sapiens from refseq
# and store the corresponding genome file in '_ncbi_downloads/collection'
Hsap_collection <- getCollection( db = "refseq",
organism = "Homo sapiens",
path = file.path("_db_downloads","collections"))
# download the collection of Homo sapiens from genbank
# and store the corresponding genome file in '_ncbi_downloads/collection'
Hsap_collection <- getCollection( db = "genbank",
organism = "Homo sapiens",
path = file.path("_db_downloads","collections"))
# download the collection of Homo sapiens from ensembl
# and store the corresponding genome file in '_ncbi_downloads/collection'
Hsap_collection <- getCollection( db = "ensembl",
organism = "Homo sapiens",
path = file.path("_db_downloads","collections"))
## End(Not run)
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