save_allele_seqs | R Documentation |
Take the alleles identified by analyze_dataset in the summary data frame and save each entry to a separate FASTA file. Samples identified as homozygous will have one sequence written rather than two. Entries with no identified alleles will be skipped.
save_allele_seqs(results_summary, dp)
results_summary |
summary data frame as produced by analyze_dataset. |
dp |
output directory path to use for all files. |
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.