From giftag to gifter
Keep the annotation step and the biological completeness decision connected, but distinct.
Pass the marker table into R
Once giftag annotate has finished, check that giftag_run.json exists and review the searchable marker count with giftag info. Then read the marker TSV:
install.packages("remotes")
remotes::install_github("alberdilab/gifter", build_vignettes = TRUE)
markers <- read.delim("annotations/giftag_markers.tsv")
needed <- c("genome_id", "gene_id", "namespace", "accession")
stopifnot(all(needed %in% names(markers)))
calls <- gifter::evaluate_gifts_community(markers)The example assumes annotations/ is the output directory used with giftag annotate -o. genome_id keeps the inputs separate, so genes in different genomes cannot combine to complete a route. For a single genome, select its marker rows and use gifter::evaluate_gifts().
CONTINUE READING IN GIFTER
The evaluating a genome guide explains complete and closest-incomplete calls, missing requirements and tracing evidence to genes. The database atlas shows the curated GIFT definitions.
What each tool establishes
| Step | Claim it can support |
|---|---|
| giftag | A gene matched a named marker profile under its source’s rule, with a recorded score and threshold. |
| gifter | The observed markers support at least one complete curated route, architecture, circuit or defense mechanism for a named GIFT. |
A positive call describes encoded capability. It does not establish expression, activity, flux, environmental relevance, actual motility, a defense outcome or phenotype. An unsupported call may reflect a missing gene, incomplete genome, search coverage gap, conservative threshold or a curated requirement with no accepted marker. Keep giftag_run.json, the built database’s giftag.json and markers.tsv, and gifter’s database version alongside the analysis so this distinction can be audited.
Where to go next
- Evaluate a genome to understand a call and trace it back to genes.
- From calls to quantitative traits for reference frames and denominators.
- A genome-resolved community to compare separately evaluated genomes.
- Many samples over one catalogue when the same catalogue is evaluated across samples.