The hardware and bandwidth for this mirror is donated by dogado GmbH, the Webhosting and Full Service-Cloud Provider. Check out our Wordpress Tutorial.
If you wish to report a bug, or if you are interested in having us mirror your free-software or open-source project, please feel free to contact us at mirror[@]dogado.de.

Running local LD operations

We have tried to provide useful cloud-based functionality for many operations, including relatively demanding LD operations. If you are running a large number of LD operations, we request that you think about performing those locally rather than through the API. We have tried to write the software to enable this to work seamlessly. Some examples below.

LD operations available on the OpenGWAS API

library(ieugwasr)
#> OpenGWAS updates:
#>   Date: 2024-05-17
#>   [>] OpenGWAS is growing!
#>   [>] Please take 2 minutes to give us feedback -
#>   [>] It will help directly shape our emerging roadmap
#>   [>] https://forms.office.com/e/eSr7EFAfCG

LD clumping

The API has a wrapper around plink version 1.90 and can use it to perform clumping with an LD reference panel from 1000 genomes reference data.

a <- tophits(id="ieu-a-2", clump=0)
b <- ld_clump(
    dplyr::tibble(rsid=a$name, pval=a$p, id=a$id)
)

There are 5 super-populations that can be requested via the pop argument. By default this will use the Europeans subset (EUR super-population). The reference panel has INDELs removed and only retains SNPs with MAF > 0.01 in the selected population.

Note that you can perform the same operation locally if you provide a path to plink and a bed/bim/fam LD reference dataset.

To get a path to plink you can do the following:

devtools::install_github("explodecomputer/genetics.binaRies")
genetics.binaRies::get_plink_binary()

To get the same LD reference dataset that is used by the API, you can download it directly from here:

http://fileserve.mrcieu.ac.uk/ld/1kg.v3.tgz

This contains an LD reference panel for each of the 5 super-populations in the 1000 genomes reference dataset. e.g. for the European super population it has the following files:

Now supposing in R you have a dataframe, dat, with the following columns:

to perform clumping, just do the following:

ld_clump(
    dplyr::tibble(rsid=dat$rsid, pval=dat$pval, id=dat$trait_id),
    plink_bin = genetics.binaRies::get_plink_binary(),
    bfile = "/path/to/reference/EUR"
)

LD matrix

Similarly, a matrix of LD r values can be generated using

ld_matrix(b$variant)

This uses the API by default but is limited to only 500 variants. You can use, instead, local plink and LD reference data in the same manner as in the ld_clump function, e.g.

ld_matrix(
    dat$rsid,
    plink_bin = genetics.binaRies::get_plink_binary(),
    bfile = "/path/to/reference/EUR"
)

LD proxies

To automatically extract variants from a dataset, and search for LD proxies when a requested variant is not present in the dataset, please look at the options available in the gwasvcf package:

https://mrcieu.github.io/gwasvcf/articles/guide.html#ld-proxies-1

These binaries (installable software) and packages are in development.
They may not be fully stable and should be used with caution. We make no claims about them.
Health stats visible at Monitor.