options(width = 750) knitr::opts_chunk$set( comment = "#>", error = FALSE, tidy = FALSE)
NOTE: To make sure that you have a sufficiently stable (internet) connection between R and the respective databases, please set the default
timeout
setting on your local machine from 60sec to at least 30000sec before running any retrieval functions via:
options(timeout = 30000)
human gut metagenome
project from NCBI Genbank
The number of genome assemblies generated and stored in sequence databases is growing exponentially every year. With the availability of this growing amount of genomic data, meta-genomics studies become more and more popular. By using this bulk of genomes for comparing them to thousands of other genomes
new structural patterns and evolutionary insights can be obtained.
However, the first step in any meta-genomics study is the retrieval of the genomes, proteomes, coding sequences or annotation files that shall be compared
and investigated. For this purpose, the meta.retrieval()
and meta.retrieval.all()
functions allows users to perform straightforward meta-genome retrieval of hundreds of genomes, proteomes, CDS, etc in R. Finally, in addition to the retrieved sequence information the meta.retrieval()
and meta.retrieval.all()
functions will
generate a summary file
which contains information about the genome version, genome status, submitter, etc for each organism to promote
computational and scientific reproducibility of the meta-genomics study at hand. This summary file
can for example be attached as Supplementary Data
to the respective study.
The meta.retrieval()
and meta.retrieval.all()
functions aim to simplify the genome retrieval and computational reproducibility process for meta-genomics studies. Both functions allow users to either download genomes, proteomes, CDS, etc for species within a specific kingdom or subgroup of life (meta.retrieval()
) or of all species of all kingdoms (meta.retrieval.all()
). Before biomartr
users had to write shell
scripts to download respective genomic data. However, since many meta-genomics packages exist for the R programming language, I implemented this functionality for easy integration into existing R workflows and for easier reproducibility.
For example, the pipeline logic of the magrittr package can be used with
meta.retrieval()
and meta.retrieval.all()
as follows.
# download all vertebrate genomes, then apply ... meta.retrieval(kingdom = "vertebrate_mammalian", db = "refseq", type = "genome") %>% ...
Here ...
denotes any subsequent meta-genomics analysis. Hence, meta.retrieval()
enables the pipeline methodology for meta-genomics.
To retrieve a list of all available kingdoms stored in the NCBI RefSeq
, NCBI Genbank
, and ENSEMBL
databases users can consult the getKingdoms()
function which stores a list of all available kingdoms of life for the corresponding database.
NCBI RefSeq
:getKingdoms(db = "refseq")
[1] "archaea" "bacteria" "fungi" "invertebrate" [5] "plant" "protozoa" "vertebrate_mammalian" "vertebrate_other" [9] "viral"
NCBI Genbank
:getKingdoms(db = "genbank")
[1] "archaea" "bacteria" "fungi" [4] "invertebrate" "plant" "protozoa" [7] "vertebrate_mammalian" "vertebrate_other"
In these examples the difference betwenn db = "refseq"
and db = "genbank"
is that db = "genbank"
does not store viral
information.
ENSEMBL
getKingdoms(db = "ensembl")
[1] "EnsemblVertebrates"
The ENSEMBL
database does not differentiate between different kingdoms, but specialized on storing high-quality reference genomes of diverse biological disciplines.
NCBI RefSeq
Download all mammalian vertebrate genomes from NCBI RefSeq
.
# download all vertebrate genomes meta.retrieval(kingdom = "vertebrate_mammalian", db = "refseq", type = "genome", reference = FALSE)
The argument kingdom
specifies the kingdom selected with getKingdoms()
from which
genomes of organisms shall be retrieved. The db
argument specifies the database
from which respective genomes shall be downloaded. The argument type
specifies
that genome assembly
files shall be retrieved. The argument reference
indicates whether or not a genome shall be downloaded if it isn't marked in the database as either a reference genome
or a representative genome
. Options are:
reference = FALSE
(Default): all organisms (reference, representative, and non-representative genomes) are downloaded.reference = TRUE
: organisms that are downloaded must be either a reference
or representative genome
. Thus, most genomes which are usually non-reference genomes will not be downloaded and the user will retrieve much less organisms than are stored in databases.When running this command all geneomes are stored in a folder which is either named according to the kingdom
(in this case vertebrate_mammalian
). Alternatively, users can specify
the out.folder
argument to define a custom output folder path.
Internally, in this example meta.retrieval()
will generate a folder named vertebrate_mammalian
in which respective genomes will be stored. In addition, the vertebrate_mammalian
folder contains a folder named documentation
which stores individual documentation
files for each individual organism and a summary file
which stores documentation
for all retrieved organisms. This summary file
can then be used as Supplementary Data
in studies to promote computational reproducibility.
An example documentation file of an individual organism looks like this:
File Name: Mus_musculus_genomic_genbank.gff.gz Organism Name: Mus_musculus Database: NCBI genbank URL: ftp://ftp.ncbi.nlm.nih.gov/genomes/all/GCA/000/001/635/GCA_000001635.7_GRCm38.p5/GCA_000001635.7_GRCm38.p5_genomic.gff.gz Download_Date: Mon Nov 14 12:43:45 2016 refseq_category: reference genome assembly_accession: GCA_000001635.7 bioproject: PRJNA20689 biosample: NA taxid: 10090 infraspecific_name: NA version_status: latest release_type: Patch genome_rep: Full seq_rel_date: 2016-06-29 submitter: Genome Reference Consortium
An example summary file
of all organism looks like this (here we use 105 Plant species as an example):
# A tibble: 105 x 16 file_name organism url database path refseq_category <chr> <chr> <chr> <chr> <chr> <chr> 1 Aegilops_tau Aegilops_ ftp://ftp.ncbi refseq Prot representative 2 Amborella_tr Amborella ftp://ftp.ncbi refseq Prot representative 3 Ananas_comos Ananas_co ftp://ftp.ncbi refseq Prot representative 4 Arabidopsis_ Arabidops ftp://ftp.ncbi refseq Prot representative 5 Arabidopsis_ Arabidops ftp://ftp.ncbi refseq Prot reference geno 6 Arachis_dura Arachis_d ftp://ftp.ncbi refseq Prot representative 7 Arachis_ipae Arachis_i ftp://ftp.ncbi refseq Prot representative 8 Asparagus_of Asparagus ftp://ftp.ncbi refseq Prot representative 9 Auxenochlore Auxenochl ftp://ftp.ncbi refseq Prot representative 10 Bathycoccus_ Bathycocc ftp://ftp.ncbi refseq Prot representative # ... with 95 more rows, and 10 more variables: assembly_accession <chr>, # bioproject <chr>, biosample <chr>, taxid <int>, # infraspecific_name <chr>, version_status <chr>, release_type <chr>, # genome_rep <chr>, seq_rel_date <date>, submitter <chr>
Unfortunately, when downloading large amounts of genomes the NCBI RefSeq database
limits the number of queries from an individual IP address. This causes
that the download process might stop or time out at a particular step.
To overcome this limitation users can simply re-run the meta.retrieval()
command they previously executed
and specify the argument restart_at_last
which has the following two options:
restart_at_last = TRUE
(Default) then meta.retrieval()
will skip all organisms that are already present in the folder and will start downloading all remaining species (thus will pick up from where the initial download process stopped). However, this way meta.retrieval()
will not be able to check whether already downloaded organism files are corrupted or not by checking the md5 checksum
of the respective file. Thus, I recommend to download the last organism before meta.retrieval()
stopped manually using getGenome()
to make sure that the respective file is not corrupted.restart_at_last = FALSE
then meta.retrieval()
will start from the beginning and crawl through already downloaded organism files and check whether already downloaded organism files are corrupted or not by checking the md5 checksum
(this procedure takes longer than restart_at_last = TRUE
). After checking existing files the function will start downloading all remaining organisms.After downloading genomes users can format the output of meta.retrieval()
by first un-zipping downloaded files and renaming them for more convenient downstream data analysis (e.g. from Saccharomyces_cerevisiae_cds_from_genomic_refseq.fna.gz
to Scerevisiae.fa
).
The easiest way to use clean.retrieval()
in combination with meta.retrieval()
is to use the pipe operator from the magrittr
package:
library(magrittr) meta.retrieval(kingdom = "vertebrate_mammalian", db = "refseq", type = "genome") %>% clean.retrieval()
In the first step, genome assembly files are downloaded with meta.retrieval
and
subsequently (%>%
) un-zipped and re-named using clean.retrieval()
.
Example Bacteria
# download all bacteria genomes meta.retrieval(kingdom = "bacteria", db = "refseq", type = "genome", reference = FALSE)
Example Viruses
# download all virus genomes meta.retrieval(kingdom = "viral", db = "refseq", type = "genome", reference = FALSE)
Example Archaea
# download all archaea genomes meta.retrieval(kingdom = "archaea", db = "refseq", type = "genome", reference = FALSE)
Example Fungi
# download all fungi genomes meta.retrieval(kingdom = "fungi", db = "refseq", type = "genome", reference = FALSE)
Example Plants
# download all plant genomes meta.retrieval(kingdom = "plant", db = "refseq", type = "genome", reference = FALSE)
Example Invertebrates
# download all invertebrate genomes meta.retrieval(kingdom = "invertebrate", db = "refseq", type = "genome", reference = FALSE)
Example Protozoa
# download all invertebrate genomes meta.retrieval(kingdom = "protozoa", db = "refseq", type = "genome", reference = FALSE)
NCBI Genbank
Alternatively, download all mammalian vertebrate genomes from NCBI Genbank
, e.g.
# download all vertebrate genomes meta.retrieval(kingdom = "vertebrate_mammalian", db = "genbank", type = "genome", reference = FALSE)
Example Bacteria
# download all bacteria genomes meta.retrieval(kingdom = "bacteria", db = "genbank", type = "genome", reference = FALSE)
Example Archaea
# download all archaea genomes meta.retrieval(kingdom = "archaea", db = "genbank", type = "genome", reference = FALSE)
Example Fungi
# download all fungi genomes meta.retrieval(kingdom = "fungi", db = "genbank", type = "genome", reference = FALSE)
Example Plants
# download all plant genomes meta.retrieval(kingdom = "plant", db = "genbank", type = "genome", reference = FALSE)
Example Invertebrates
# download all invertebrate genomes meta.retrieval(kingdom = "invertebrate", db = "genbank", type = "genome", reference = FALSE)
Example Protozoa
# download all invertebrate genomes meta.retrieval(kingdom = "protozoa", db = "genbank", type = "genome", reference = FALSE)
ENSEMBL
# download all genomes from ENSEMBL meta.retrieval(kingdom = "Ensembl", db = "ensembl", type = "genome", reference = FALSE)
In case users do not wish to retrieve genomes from an entire kingdom, but rather from
a group or subgoup (e.g. from species belonging to the Gammaproteobacteria
class, a subgroup of the bacteria
kingdom), they can use the following workflow.
Gammaproteobacteria
genomes from NCBI RefSeq
:First, users can again consult the getKingdoms()
function to retrieve kingdom information.
getKingdoms(db = "refseq")
[1] "archaea" "bacteria" "fungi" "invertebrate" [5] "plant" "protozoa" "vertebrate_mammalian" "vertebrate_other" [9] "viral"
In this example, we will choose the bacteria
kingdom. Now, the getGroups()
function allows users to obtain
available subgroups of the bacteria
kingdom.
getGroups(db = "refseq", kingdom = "bacteria")
[1] "Acidithiobacillia" "Acidobacteriia" [3] "Actinobacteria" "Alphaproteobacteria" [5] "Aquificae" "Armatimonadetes" [7] "Bacteroidetes/Chlorobi group" "Balneolia" [9] "Betaproteobacteria" "Blastocatellia" [11] "Candidatus Kryptonia" "Chlamydiae" [13] "Chloroflexi" "Cyanobacteria/Melainabacteria group" [15] "Deinococcus-Thermus" "delta/epsilon subdivisions" [17] "Endomicrobia" "Fibrobacteres" [19] "Firmicutes" "Fusobacteriia" [21] "Gammaproteobacteria" "Gemmatimonadetes" [23] "Kiritimatiellaeota" "Nitrospira" [25] "Planctomycetes" "Spirochaetia" [27] "Synergistia" "Tenericutes" [29] "Thermodesulfobacteria" "Thermotogae" [31] "unclassified Acidobacteria" "unclassified Bacteria (miscellaneous)" [33] "unclassified Proteobacteria" "Verrucomicrobia" [35] "Zetaproteobacteria"
Please note, that the kingdom
argument specified in getGroups()
needs to match with an available kingdom retrieved with getKingdoms()
.
It is also important that in both cases: getKingdoms()
and getGroups()
the same database should be specified.
Now we choose the group Gammaproteobacteria
and specify the group
argument in the meta.retrieval()
function.
meta.retrieval(kingdom = "bacteria", group = "Gammaproteobacteria", db = "refseq", type = "genome", reference = FALSE)
Using this command, all bacterial (kingdom = "bacteria"
) genomes (type = "genome"
) that belong to the group Gammaproteobacteria
(group = "Gammaproteobacteria"
) will be retrieved from NCBI RefSeq (db = "refseq"
).
Alternatively, Gammaproteobacteria
genomes can be retrieved from NCBI Genbank by exchanging db = "refseq"
to db = "genbank"
.
If users wish to download proteome, CDS, or GFF files instead of genomes, they can specify the argument: type = "proteome"
, type = "cds"
, or type = "gff"
.
Adenoviridae
genomes from NCBI RefSeq
:Retrieve groups for viruses.
getGroups(db = "refseq", kingdom = "viral")
[1] "Adenoviridae" "Alloherpesviridae" [3] "Alphaflexiviridae" "Alphatetraviridae" [5] "Alvernaviridae" "Amalgaviridae" [7] "Ampullaviridae" "Anelloviridae" [9] "Apple fruit crinkle viroid" "Apple hammerhead viroid-like circular RNA" [11] "Apscaviroid" "Arenaviridae" [13] "Arteriviridae" "Ascoviridae" [15] "Asfarviridae" "Astroviridae" [17] "Avsunviroid" "Baculoviridae" [19] "Barnaviridae" "Benyviridae" [21] "Betaflexiviridae" "Bicaudaviridae" [23] "Birnaviridae" "Bornaviridae" [25] "Bromoviridae" "Bunyaviridae" [27] "Caliciviridae" "Carmotetraviridae" [29] "Caulimoviridae" "Cherry leaf scorch small circular viroid-like RNA 1" [31] "Cherry small circular viroid-like RNA" "Chrysoviridae" [33] "Circoviridae" "Closteroviridae" [35] "Cocadviroid" "Coleviroid" [37] "Coronaviridae" "Corticoviridae" [39] "Cystoviridae" "Dicistroviridae" [41] "Elaviroid" "Endornaviridae" [43] "Filoviridae" "Flaviviridae" [45] "Fusarividae" "Fuselloviridae" [47] "Gammaflexiviridae" "Geminiviridae" [49] "Genomoviridae" "Globuloviridae" [51] "Grapevine latent viroid" "Guttaviridae" [53] "Hepadnaviridae" "Hepeviridae" [55] "Herpesviridae" "Hostuviroid" [57] "Hypoviridae" "Hytrosaviridae" [59] "Iflaviridae" "Inoviridae" [61] "Iridoviridae" "Lavidaviridae" [63] "Leviviridae" "Lipothrixviridae" [65] "Luteoviridae" "Malacoherpesviridae" [67] "Marnaviridae" "Marseilleviridae" [69] "Megabirnaviridae" "Mesoniviridae" [71] "Microviridae" "Mimiviridae" [73] "Mulberry small circular viroid-like RNA 1" "Mymonaviridae" [75] "Myoviridae" "Nanoviridae" [77] "Narnaviridae" "Nimaviridae" [79] "Nodaviridae" "Nudiviridae" [81] "Nyamiviridae" "Ophioviridae" [83] "Orthomyxoviridae" "Other" [85] "Papillomaviridae" "Paramyxoviridae" [87] "Partitiviridae" "Parvoviridae" [89] "Pelamoviroid" "Permutotetraviridae" [91] "Persimmon viroid" "Phycodnaviridae" [93] "Picobirnaviridae" "Picornaviridae" [95] "Plasmaviridae" "Pneumoviridae" [97] "Podoviridae" "Polydnaviridae" [99] "Polyomaviridae" "Pospiviroid" [101] "Potyviridae" "Poxviridae" [103] "Quadriviridae" "Reoviridae" [105] "Retroviridae" "Rhabdoviridae" [107] "Roniviridae" "Rubber viroid India/2009" [109] "Rudiviridae" "Secoviridae" [111] "Siphoviridae" "Sphaerolipoviridae" [113] "Sunviridae" "Tectiviridae" [115] "Togaviridae" "Tombusviridae" [117] "Totiviridae" "Turriviridae" [119] "Tymoviridae" "unclassified" [121] "unclassified Pospiviroidae" "Virgaviridae"
Now we can choose Adenoviridae
as group argument for the meta.retrieval()
function.
meta.retrieval(kingdom = "viral", group = "Adenoviridae", db = "refseq", type = "genome", reference = FALSE)
Again, by exchanging type = "genome"
by either type = "proteome"
, type = "cds"
, type = "rna"
, type = "assemblystats"
, or type = "gff"
, users can retrieve proteome, CDS, RNA, genome assembly statistics or GFF files instead of genomes.
Although much effort is invested to increase the genome assembly quality when new genomes are published or new versions are released, the influence of genome assembly quality on downstream analyses cannot be neglected. A rule of thumb is, that the larger the genome the more prone it is to genome assembly errors and therefore, a reduction of assembly quality.
In Veeckman et al., 2016 the authors conclude:
As yet, no uniform metrics or standards are in place to estimate the completeness of a genome assembly or the annotated gene space, despite their importance for downstream analyses
In most metagenomics studies, however, the influence or bias of genome assembly quality on the outcome of the analysis (e.g. comparative genomics, annotation, etc.) is neglected. To better grasp the genome assembly quality, the NCBI databases store genome assembly statistics of some species for which genome assemblies are available. An example assembly statistics report can be found at: ftp://ftp.ncbi.nlm.nih.gov/genomes/all/GCF/000/001/405/GCF_000001405.36_GRCh38.p10/GCF_000001405.36_GRCh38.p10_assembly_stats.txt.
The biomartr
package allows users to retrieve these genome assembly stats file in an automated way by specifying the argument type = "assemblystats"
and combine = TRUE
.
Please make sure that combine = TRUE
when selecting type = "assemblystats"
.
# show all elements of the data.frame options(tibble.print_max = Inf) # retrieve genome assembly stats for all mammal genome assemblies # and store these stats in a data.frame mammals.gc <- meta.retrieval(kingdom = "vertebrate_mammalian", db = "refseq", type = "assemblystats", combine = TRUE) mammals.gc
species total_length spanned_gaps unspanned_gaps region_count scaffold_count <chr> <int> <int> <int> <int> <int> 1 Ornithorhynchus anatinus 1995607322 243698 137 0 200283 2 Sarcophilus harrisii NA 201317 0 0 35974 3 Dasypus novemcinctus NA 268413 0 0 46559 4 Erinaceus europaeus NA 219764 0 0 5803 5 Echinops telfairi NA 269444 0 0 8402 6 Pteropus alecto 1985975446 104566 0 0 65598 7 Rousettus aegyptiacus 1910250568 559 0 0 NA 8 Callithrix jacchus NA 184972 2242 0 16399 9 Cebus capucinus imitator NA 133441 0 0 7156 10 Cercocebus atys NA 65319 0 0 11433 # ... with 89 more rows, and 9 more variables: scaffold_N50 <int>, scaffold_L50 <int>, # scaffold_N75 <int>, scaffold_N90 <int>, contig_count <int>, contig_N50 <int>, total_gap_length <int>, # molecule_count <int>, top_level_count <int>
Analogously, this information can be retrieved for each kingdom other than kingdom = "vertebrate_mammalian"
. Please consult getKingdoms()
for available kingdoms.
NCBI Genbank stores metagenome projects in addition to species specific genome, proteome or CDS sequences. To retrieve these metagenomes users can perform the following combination of commands:
First, users can list the project names of available metagenomes by typing
# list available metagenomes at NCBI Genbank listMetaGenomes()
[1] "metagenome" "human gut metagenome" "epibiont metagenome" [4] "marine metagenome" "soil metagenome" "mine drainage metagenome" [7] "mouse gut metagenome" "marine sediment metagenome" "termite gut metagenome" [10] "hot springs metagenome" "human lung metagenome" "fossil metagenome" [13] "freshwater metagenome" "saltern metagenome" "stromatolite metagenome" [16] "coral metagenome" "mosquito metagenome" "fish metagenome" [19] "bovine gut metagenome" "chicken gut metagenome" "wastewater metagenome" [22] "microbial mat metagenome" "freshwater sediment metagenome" "human metagenome" [25] "hydrothermal vent metagenome" "compost metagenome" "wallaby gut metagenome" [28] "groundwater metagenome" "gut metagenome" "sediment metagenome" [31] "ant fungus garden metagenome" "food metagenome" "hypersaline lake metagenome" [34] "hydrocarbon metagenome" "activated sludge metagenome" "viral metagenome" [37] "bioreactor metagenome" "wasp metagenome" "permafrost metagenome" [40] "sponge metagenome" "aquatic metagenome" "insect gut metagenome" [43] "activated carbon metagenome" "anaerobic digester metagenome" "rock metagenome" [46] "terrestrial metagenome" "rock porewater metagenome" "seawater metagenome" [49] "scorpion gut metagenome" "soda lake metagenome" "glacier metagenome"
Internally the listMetaGenomes()
function downloads the assembly_summary.txt file from ftp://ftp.ncbi.nlm.nih.gov/genomes/genbank/metagenomes/ to retrieve
available metagenome information. This procedure might take a few seconds during the first run of listMetaGenomes()
. Subsequently, the assembly_summary.txt file will be stored in the tempdir()
directory to
achieve a much faster access of this information during following uses of listMetaGenomes()
.
In case users wish to retrieve detailed information about available metagenome projects they can specify the details = TRUE
argument.
# show all elements of the data.frame options(tibble.print_max = Inf) # detailed information on available metagenomes at NCBI Genbank listMetaGenomes(details = TRUE)
# A tibble: 857 x 21 assembly_accession bioproject biosample wgs_master refseq_category taxid species_taxid <chr> <chr> <chr> <chr> <chr> <int> <int> 1 GCA_000206185.1 PRJNA32359 SAMN02954317 AAGA00000000.1 na 256318 256318 2 GCA_000206205.1 PRJNA32355 SAMN02954315 AAFZ00000000.1 na 256318 256318 3 GCA_000206225.1 PRJNA32357 SAMN02954316 AAFY00000000.1 na 256318 256318 4 GCA_000208265.2 PRJNA17779 SAMN02954240 AASZ00000000.1 na 256318 256318 5 GCA_000208285.1 PRJNA17657 SAMN02954268 AATO00000000.1 na 256318 256318 6 GCA_000208305.1 PRJNA17659 SAMN02954269 AATN00000000.1 na 256318 256318 7 GCA_000208325.1 PRJNA16729 SAMN02954263 AAQL00000000.1 na 256318 256318 8 GCA_000208345.1 PRJNA16729 SAMN02954262 AAQK00000000.1 na 256318 256318 9 GCA_000208365.1 PRJNA13699 SAMN02954283 AAFX00000000.1 na 256318 256318 10 GCA_900010595.1 PRJEB11544 SAMEA3639840 CZPY00000000.1 na 256318 256318 # ... with 847 more rows, and 14 more variables: organism_name <chr>, infraspecific_name <chr>, # isolate <chr>, version_status <chr>, assembly_level <chr>, release_type <chr>, genome_rep <chr>, # seq_rel_date <date>, asm_name <chr>, submitter <chr>, gbrs_paired_asm <chr>, paired_asm_comp <chr>, # ftp_path <chr>, excluded_from_refseq <chr>
Finally, users can retrieve available metagenomes using getMetaGenomes()
. The name
argument receives the metagenome project name retrieved with listMetaGenomes()
.
The path
argument specifies the folder path in which corresponding genomes shall be stored.
# retrieve all genomes belonging to the human gut metagenome project getMetaGenomes(name = "human gut metagenome", path = file.path("_ncbi_downloads","human_gut"))
1] "The metagenome of 'human gut metagenome' has been downloaded to '_ncbi_downloads/human_gut'." [1] "_ncbi_downloads/human_gut/GCA_000205525.2_ASM20552v2_genomic.fna.gz" [2] "_ncbi_downloads/human_gut/GCA_000205765.1_ASM20576v1_genomic.fna.gz" [3] "_ncbi_downloads/human_gut/GCA_000205785.1_ASM20578v1_genomic.fna.gz" [4] "_ncbi_downloads/human_gut/GCA_000207925.1_ASM20792v1_genomic.fna.gz" [5] "_ncbi_downloads/human_gut/GCA_000207945.1_ASM20794v1_genomic.fna.gz" [6] "_ncbi_downloads/human_gut/GCA_000207965.1_ASM20796v1_genomic.fna.gz" [7] "_ncbi_downloads/human_gut/GCA_000207985.1_ASM20798v1_genomic.fna.gz" [8] "_ncbi_downloads/human_gut/GCA_000208005.1_ASM20800v1_genomic.fna.gz" [9] "_ncbi_downloads/human_gut/GCA_000208025.1_ASM20802v1_genomic.fna.gz" [10] "_ncbi_downloads/human_gut/GCA_000208045.1_ASM20804v1_genomic.fna.gz" [11] "_ncbi_downloads/human_gut/GCA_000208065.1_ASM20806v1_genomic.fna.gz" [12] "_ncbi_downloads/human_gut/GCA_000208085.1_ASM20808v1_genomic.fna.gz" [13] "_ncbi_downloads/human_gut/GCA_000208105.1_ASM20810v1_genomic.fna.gz" [14] "_ncbi_downloads/human_gut/GCA_000208125.1_ASM20812v1_genomic.fna.gz" [15] "_ncbi_downloads/human_gut/GCA_000208145.1_ASM20814v1_genomic.fna.gz" [16] "_ncbi_downloads/human_gut/GCA_000208165.1_ASM20816v1_genomic.fna.gz" ...
Internally, getMetaGenomes()
creates a folder specified in the path
argument.
Genomes associated with the metagenomes project specified in the name
argument
will then be downloaded and stored in this folder. As return value getMetaGenomes()
returns the file paths to the genome files which can then be used as input to the read*()
functions.
Alternatively or subsequent to the metagenome retrieval, users can retrieve annotation files of genomes belonging to a metagenome project
selected with listMetaGenomes()
by using the getMetaGenomeAnnotations()
function.
# retrieve all genomes belonging to the human gut metagenome project getMetaGenomeAnnotations(name = "human gut metagenome", path = file.path("_ncbi_downloads","human_gut","annotations"))
[1] "The annotations of metagenome 'human gut metagenome' have been downloaded and stored at '_ncbi_downloads/human_gut/annotations'." [1] "_ncbi_downloads/human_gut/annotations/GCA_000205525.2_ASM20552v2_genomic.gff.gz" [2] "_ncbi_downloads/human_gut/annotations/GCA_000205765.1_ASM20576v1_genomic.gff.gz" [3] "_ncbi_downloads/human_gut/annotations/GCA_000205785.1_ASM20578v1_genomic.gff.gz" [4] "_ncbi_downloads/human_gut/annotations/GCA_000207925.1_ASM20792v1_genomic.gff.gz" [5] "_ncbi_downloads/human_gut/annotations/GCA_000207945.1_ASM20794v1_genomic.gff.gz" [6] "_ncbi_downloads/human_gut/annotations/GCA_000207965.1_ASM20796v1_genomic.gff.gz" [7] "_ncbi_downloads/human_gut/annotations/GCA_000207985.1_ASM20798v1_genomic.gff.gz" [8] "_ncbi_downloads/human_gut/annotations/GCA_000208005.1_ASM20800v1_genomic.gff.gz" [9] "_ncbi_downloads/human_gut/annotations/GCA_000208025.1_ASM20802v1_genomic.gff.gz" [10] "_ncbi_downloads/human_gut/annotations/GCA_000208045.1_ASM20804v1_genomic.gff.gz" [11] "_ncbi_downloads/human_gut/annotations/GCA_000208065.1_ASM20806v1_genomic.gff.gz" [12] "_ncbi_downloads/human_gut/annotations/GCA_000208085.1_ASM20808v1_genomic.gff.gz" [13] "_ncbi_downloads/human_gut/annotations/GCA_000208105.1_ASM20810v1_genomic.gff.gz" [13] "_ncbi_downloads/human_gut/annotations/GCA_000208105.1_ASM20810v1_genomic.gff.gz" [14] "_ncbi_downloads/human_gut/annotations/GCA_000208125.1_ASM20812v1_genomic.gff.gz" [15] "_ncbi_downloads/human_gut/annotations/GCA_000208145.1_ASM20814v1_genomic.gff.gz" [16] "_ncbi_downloads/human_gut/annotations/GCA_000208165.1_ASM20816v1_genomic.gff.gz" ...
The file paths of the downloaded *.gff
are retured by getMetaGenomeAnnotations()
and can be used
as input for the read.gff()
function in the seqreadr package.
Download all mammalian vertebrate proteomes.
NCBI RefSeq
:# download all vertebrate genomes meta.retrieval(kingdom = "vertebrate_mammalian", db = "refseq", type = "proteome", reference = FALSE)
NCBI Genbank
:# download all vertebrate genomes meta.retrieval(kingdom = "vertebrate_mammalian", db = "genbank", type = "proteome", reference = FALSE)
ENSEMBL
:# download all Ensembl proteome sequneces meta.retrieval(kingdom = "Ensembl", db = "ensembl", type = "proteome", reference = FALSE)
Download all mammalian vertebrate CDS from RefSeq (Genbank does not store CDS data).
NCBI RefSeq
:# download all vertebrate genomes meta.retrieval(kingdom = "vertebrate_mammalian", db = "refseq", type = "cds", reference = FALSE)
NCBI Genbank
:# download all vertebrate genomes meta.retrieval(kingdom = "vertebrate_mammalian", db = "genbank", type = "cds", reference = FALSE)
ENSEMBL
:# download all Ensembl CDS sequneces meta.retrieval(kingdom = "Ensembl", db = "ensembl", type = "cds", reference = FALSE)
Download all mammalian vertebrate gff files.
Example NCBI RefSeq
:
# download all vertebrate gff files meta.retrieval(kingdom = "vertebrate_mammalian", db = "refseq", type = "gff", reference = FALSE)
Example NCBI Genbank
:
# download all vertebrate gff files meta.retrieval(kingdom = "vertebrate_mammalian", db = "genbank", type = "gff", reference = FALSE)
Download all mammalian vertebrate gtf files.
Example ENSEMBL
:
# download all vertebrate gff files meta.retrieval(kingdom = "Ensembl", db = "ensembl", type = "gtf", reference = FALSE)
Download all mammalian vertebrate RNA sequences from NCBI RefSeq
and NCBI Genbank
.
NCBI RefSeq
:# download all vertebrate RNA sequneces meta.retrieval(kingdom = "vertebrate_mammalian", db = "refseq", type = "rna", reference = FALSE)
NCBI Genbank
:# download all vertebrate RNA sequneces meta.retrieval(kingdom = "vertebrate_mammalian", db = "genbank", type = "rna", reference = FALSE)
ENSEMBL
:# download all Ensembl RNA sequneces meta.retrieval(kingdom = "Ensembl", db = "ensembl", type = "rna", reference = FALSE)
Download all mammalian vertebrate Repeat Masker Annotation files from NCBI RefSeq
and NCBI Genbank
.
NCBI RefSeq
:# download all vertebrate RNA sequneces meta.retrieval(kingdom = "vertebrate_mammalian", db = "refseq", type = "rm", reference = FALSE)
NCBI Genbank
:# download all vertebrate RNA sequneces meta.retrieval(kingdom = "vertebrate_mammalian", db = "genbank", type = "rm", reference = FALSE)
Users can obtain alternative kingdoms using getKingdoms()
.
If users wish to download the all genomes, proteome, CDS, or gff files for all species
available in RefSeq or Genbank, they can use the meta.retrieval.all()
function for this purpose.
Example RefSeq
:
# download all geneomes stored in RefSeq meta.retrieval.all(db = "refseq", type = "genome", reference = FALSE)
Example Genbank
:
# download all geneomes stored in Genbank meta.retrieval.all(db = "genbank", type = "genome", reference = FALSE)
Example RefSeq
:
# download all proteome stored in RefSeq meta.retrieval.all(db = "refseq", type = "proteome", reference = FALSE)
Example Genbank
:
# download all proteome stored in Genbank meta.retrieval.all(db = "genbank", type = "proteome", reference = FALSE)
Again, by exchanging type = "proteome"
by either
type = "genome"
type = "cds"
type = "rna"
type = "assemblystats"
type = "gff"
users can retrieve genome, CDS, RNA, genome assembly statistics or GFF files instead of proteomes.
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