getGenomeSet | R Documentation |
Main genome retrieval function for a set of organism of interest. By specifying the scientific names of the organisms of interest the corresponding fasta-files storing the genome of the organisms of interest will be downloaded and stored locally. Genome files can be retrieved from several databases.
getGenomeSet(
db = "refseq",
organisms,
reference = FALSE,
release = NULL,
skip_bacteria = TRUE,
gunzip = TRUE,
update = FALSE,
path = "set_genomes",
assembly_type = "toplevel",
mute_citation = FALSE
)
db |
a character string specifying the database from which the genome shall be retrieved:
|
organisms |
a character vector storing the names of the organisms than shall be retrieved. There are three available 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. |
release |
a numeric, the database release version of ENSEMBL ( |
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 |
gunzip |
a logical, indicating whether or not files should be unzipped. |
update |
logical, default FALSE. Updated backend cached files needed. Usually keep this false, to make ut run much faster. Only set to TRUE, if you believe you cache is outdated (Species only exist in newest release etc) |
path |
a character string specifying the location (a folder) in which
the corresponding genomes shall be stored. Default is
|
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 |
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
character vector, the file path to the downloaded genomes,
The returned character vector has names as either:
- 'new' (file was downloaded now)
- 'old' files did already exist)
Hajk-Georg Drost
Other getBioSet:
getBioSet()
,
getCDSSet()
,
getCollectionSet()
,
getGFFSet()
,
getProteomeSet()
,
getRNASet()
Other genome:
getGenome()
,
read_genome()
## Not run:
getBioSet("refseq", organisms = c("Arabidopsis thaliana",
"Arabidopsis lyrata",
"Capsella rubella"),
set_type = "cds")
## End(Not run)
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