STACAS
Single-cell batch correction that learned to use cell labels, then spent three releases chasing Seurat.
A side-by-side editorial comparison of b3gbi and GeneNMF — release velocity, themes, recent moves, and the top alternatives to consider.
b3gbi pulled confidence intervals out of its indicator workflow and handed them to dubicube.
b3gbi computes biodiversity indicators from GBIF occurrence cubes for the B-Cubed project, and sits at 0.9.4 in a JOSS review run-up. The 0.9 release decoupled uncertainty from indicator calculation: confidence intervals are no longer produced inline but added afterward with add_ci(), backed by whole-cube bootstrapping from the sibling dubicube package. Everything since has been grid-parsing and compatibility repair around that split.
GeneNMF rebuilt how it derives meta-programs, changing every result it had produced.
GeneNMF applies non-negative matrix factorization to single-cell expression data to find gene programs, then consolidates programs recurring across samples into meta-programs. Version 0.6.0 replaced the consolidation method: instead of reducing each program to a gene set and taking a consensus, it retains full gene weight vectors and compares them by cosine similarity. Later releases have built reporting and control around that core — a metaprogram composition matrix showing which samples contributed, custom signature databases for enrichment testing, and the ability to drop meta-programs from results.
b3gbi computes biodiversity indicators from GBIF occurrence cubes for the B-Cubed project, and sits at 0.9.4 in a JOSS review run-up. The 0.9 release decoupled uncertainty from indicator calculation: confidence intervals are no longer produced inline but added afterward with add_ci(), backed by whole-cube bootstrapping from the sibling dubicube package. Everything since has been grid-parsing and compatibility repair around that split.
Two forces are shaping releases. Internally, the uncertainty split produced an indicator-specific rule book — species-level indicators bootstrap the whole cube, raw counts resample within year, evenness gets a logit transform — and that rule book is where the statistical thinking now lives. Externally, GBIF's taxonomic backbone migration to the Catalogue of Life forced string taxon keys through process_cube() and the plotting paths, while recurring EEA and MGRS grid-code fixes mark coordinate parsing as the least settled area.
The 0.9.4 notes are entirely JOSS review items — contributors, examples, tracked datasets — so the next release is most likely a JOSS-accepted 1.0 rather than new indicator work.
GeneNMF applies non-negative matrix factorization to single-cell expression data to find gene programs, then consolidates programs recurring across samples into meta-programs. Version 0.6.0 replaced the consolidation method: instead of reducing each program to a gene set and taking a consensus, it retains full gene weight vectors and compares them by cosine similarity. Later releases have built reporting and control around that core — a metaprogram composition matrix showing which samples contributed, custom signature databases for enrichment testing, and the ability to drop meta-programs from results.
The package is moving from producing meta-programs to letting users interrogate and constrain how they were formed. Composition matrices, the drop function and downsampled similarity heatmaps all serve inspection rather than derivation. The parameters added alongside the 0.6.0 rewrite — specificity weighting, cumulative weight thresholds, confidence defined as the fraction of programs containing a gene — turn what were fixed internal choices into stated, tunable ones.
Recent releases have been fixes and compatibility work rather than method changes, so the core approach appears settled. The dependency on an RcppML version not on CRAN is the loose end most likely to force the next release.
Other Analytics products tracked by Sparkpulse, ranked by recent ship velocity. Each card links to a full editorial trajectory and lets you pivot into a head-to-head comparison with either b3gbi or GeneNMF.
Single-cell batch correction that learned to use cell labels, then spent three releases chasing Seurat.
A debugger for ggplot2's internals, hardening its grip as the internals it traces keep moving.
A univariate density estimator that added zero-inflated data and reopened its C++ API to do it.
Stationary vine copulas for time series, released in lockstep with the rest of Nagler's vine stack.
A single-purpose ggplot2 extension that has spent six years tracking ggplot2 instead of growing.
A Star Trek data package that became a Memory Alpha web client and has been patching scrapers ever since.
See all b3gbi alternatives → · See all GeneNMF alternatives →
Latest ship moves from both products, interleaved chronologically. ⚡ = editorial spark.
They serve adjacent needs but don't currently overlap on shipped themes. b3gbi is currently shipping more aggressively (velocity 2.5 vs 0.0), with 0 editorial sparks in the last 30 days against 0. See the at-a-glance table above for a side-by-side breakdown of velocity, recent sparks, and editorial themes.
Sparkpulse doesn't pick a winner — we score release velocity, not feature parity. b3gbi is currently shipping more aggressively (velocity 2.5 vs 0.0), with 0 editorial sparks in the last 30 days against 0. For your specific use case, the alternatives sections above list other Analytics products to evaluate alongside.
Top b3gbi alternatives in Analytics are ranked by recent ship velocity. Browse the "b3gbi alternatives" section above for the current picks, or visit /alternatives/b3gbi for the full list with editorial commentary on each.
Top GeneNMF alternatives in Analytics are ranked by recent ship velocity. Browse the "GeneNMF alternatives" section above for the current picks, or visit /alternatives/genenmf for the full list with editorial commentary on each.