rsnps
This package gives you access to data from OpenSNP and NCBI’s dbSNP SNP database.
NOTE
rsnps
used to be ropensnp
Data sources
This set of functions/package accesses data from:
- openSNP.org
- https://opensnp.org
- See documentation on the openSNP API https://opensnp.org/faq#api
- See blog post about their API https://opensnp.wordpress.com/2012/01/18/some-progress-on-the-api-json-endpoints/
- Relevant functions:
allgensnp()
,allphenotypes()
,annotations()
,download_users()
,fetch_genotypes()
,genotypes()
,phenotypes()
,phenotypes_byid()
,users()
- NCBI’s dbSNP SNP database
- See https://www.ncbi.nlm.nih.gov/snp/ for more details
- Relevant function:
ncbi_snp_query()
Install
Install from CRAN
install.packages("rsnps")
Or dev version
install.packages("remotes")
remotes::install_github("ropensci/rsnps")
library("rsnps")
Usage
NCBI dbSNP data
snps <- c("rs332", "rs420358", "rs1837253", "rs1209415715", "rs111068718")
ncbi_snp_query(snps)
#> # A tibble: 4 × 16
#> query chromosome bp class rsid gene alleles ancestral_allele
#> <chr> <chr> <dbl> <chr> <chr> <chr> <chr> <chr>
#> 1 rs332 7 117559593 del rs1219… "CFT… TTT, d… TTT
#> 2 rs420358 1 40341239 snv rs4203… "" A,C,G,T A
#> 3 rs1837253 5 111066174 snv rs1837… "" T,C T
#> 4 rs1209415715 9 41782316 snv rs1209… "" T,A,C T
#> # ℹ 8 more variables: variation_allele <chr>, seqname <chr>, hgvs <chr>,
#> # assembly <chr>, ref_seq <chr>, minor <chr>, maf <dbl>,
#> # maf_population <list>
The ncbi_snp_query()
function can be used with an NCBI API which gives
access higher numbers of API requests per second. More information about
setting this up can be found in the package help accessed via ?rsnps
.
openSNP data
genotypes()
function
genotypes('rs9939609', userid='1,6,8', df=TRUE)
#> snp_name snp_chromosome snp_position user_name user_id
#> 1 rs9939609 16 53786615 Bastian Greshake Tzovaras 1
#> 2 rs9939609 16 53786615 Nash Parovoz 6
#> 3 rs9939609 16 53786615 Samantha B. Clark 8
#> genotype_id genotype
#> 1 9 AT
#> 2 5 AT
#> 3 2 TT
phenotypes()
function
out <- phenotypes(userid=1)
out$phenotypes$`Hair Type`
#> $phenotype_id
#> [1] 16
#>
#> $variation
#> [1] "straight"
For more detail, see the vignette: rsnps tutorial.
Meta
- Please report any issues or bugs.
- License: MIT
- Get citation information for
rsnsps
in R doingcitation(package = 'rsnps')
- Please note that this package is released with a Contributor Code of Conduct. By contributing to this project, you agree to abide by its terms.