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mirror of https://github.com/msberends/AMR.git synced 2026-05-31 21:01:45 +02:00

Add parallel computing support to antibiogram() and wisca() (#281)

For WISCA: simulations are distributed across (group, chunk) job pairs
via future.apply::future_lapply(), keeping all workers active even when
the regimen count is smaller than nbrOfWorkers(). Sequential fallback
with progress ticker is preserved when parallel = FALSE or workers = 1.

For grouped antibiograms: each group is processed by a separate worker,
mirroring the row-batch approach in as.sir().

Same gate pattern as as.sir() (PR #280): requires a non-sequential
future::plan() to be active; auto-upgrades to parallel = TRUE when a
parallel plan is detected; throws an informative error otherwise.

https://claude.ai/code/session_01FC43syPbzhGmKgrrVNHjnF
This commit is contained in:
Claude
2026-04-30 10:12:36 +00:00
parent 23beebc6c3
commit 623f6230f9
4 changed files with 253 additions and 70 deletions

View File

@@ -1,4 +1,4 @@
# AMR 3.0.1.9053
# AMR 3.0.1.9050
This will become release v3.1.0, intended for launch end of May.
@@ -7,6 +7,7 @@ This will become release v3.1.0, intended for launch end of May.
* Support for the [`future`](https://future.futureverse.org) package and its framework, as the previous implementation of parallel computing was slow
- **Breaking change**: `as.sir()` with `parallel = TRUE` now requires a non-sequential `future::plan()` to be active before the call — e.g., `future::plan(future::multisession)` — and throws an informative error if none is set.
- New all-core usage setup: when the number of AB columns is smaller than the number of available cores, rows are now split into batches so all cores stay active (row-batch mode). Previously, a 6-column dataset on a 16-core machine would only use 6 cores; now all 16 are used, with each worker processing a smaller row slice (lower per-worker memory pressure and processing time)
- `antibiogram()` and `wisca()` gained a `parallel` argument using the same `future`/`future.apply` pattern: for WISCA, Monte Carlo simulations are split into `(group, chunk)` job pairs distributed across workers; for grouped antibiograms, each group is processed by a separate worker (#281)
* Integration with the *tidymodels* framework to allow seamless use of SIR, MIC and disk data in modelling pipelines via `recipes`
- `step_mic_log2()` to transform `<mic>` columns with log2, and `step_sir_numeric()` to convert `<sir>` columns to numeric
- New `tidyselect` helpers: