tools for exploring 1000 genomes with R
This is an R package that contains some metadata and some functions to interrogate aspects of the S3 bucket containing 1000 genomes sequencing and variant data.
Currently we have
get_readme
to retrieve README text files to the R sessionlowcov_bam_urls
to generate URLs to low coverage alignment files in BAM formatA vignette is available with more details.
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