fillpattern
Pattern fills for ggplot2, hardened against the ways users write sizes
A side-by-side editorial comparison of qtl2convert and UCell — release velocity, themes, recent moves, and the top alternatives to consider.
A conversion utility in pure maintenance mode, tracking R-devel breakage release by release
qtl2convert is the format-shim of the R/qtl2 ecosystem: it moves genotype probabilities and genetic maps between DOQTL, R/qtl and R/qtl2 representations. The last three releases contain no new conversion functions at all — 0.32 fixed a C string comparison flagged by CRAN, 0.34 restored attribute-clearing that R-devel 4.7 changed underneath the package, and 0.36 adjusted parallel core defaults plus a test tweak. The functional surface has been stable since 0.26 added cross2_ril_to_genril().
A rank-based gene signature scorer that has grown by adapting to whatever object format single-cell R uses next
UCell scores gene signatures in single-cell data using a rank-based metric that is robust to dataset composition. Its release history reads as a sequence of ecosystem accommodations: Bioconductor submission in 2.0, SmoothKNN() for k-nearest-neighbor smoothing of scores in 2.2, smoothing applied directly to expression slots in 2.4, Seurat v5 assay compatibility in 2.6, multi-layer Seurat v5 objects in 2.8, and a missing_genes parameter in 2.14 that lets callers impute or skip signature genes absent from the data. Version 2.16 tracks Bioconductor 3.23 and points at a new publication and a Python implementation, pyUCell.
qtl2convert is the format-shim of the R/qtl2 ecosystem: it moves genotype probabilities and genetic maps between DOQTL, R/qtl and R/qtl2 representations. The last three releases contain no new conversion functions at all — 0.32 fixed a C string comparison flagged by CRAN, 0.34 restored attribute-clearing that R-devel 4.7 changed underneath the package, and 0.36 adjusted parallel core defaults plus a test tweak. The functional surface has been stable since 0.26 added cross2_ril_to_genril().
This is a package whose release cadence is driven by its dependencies, not its roadmap. Two of the last three releases exist purely because upstream R or CRAN's check suite moved; the maintainer responds within weeks and ships. The cores=0 change in 0.36 is the only user-visible behavior shift in over a year, and it landed simultaneously in sibling package qtl2fst — this is a maintainer-wide convention change, not a qtl2convert decision.
Expect the next release to be triggered by another R-devel or CRAN check change rather than a feature request, following the same pattern as 0.32 and 0.34.
UCell scores gene signatures in single-cell data using a rank-based metric that is robust to dataset composition. Its release history reads as a sequence of ecosystem accommodations: Bioconductor submission in 2.0, SmoothKNN() for k-nearest-neighbor smoothing of scores in 2.2, smoothing applied directly to expression slots in 2.4, Seurat v5 assay compatibility in 2.6, multi-layer Seurat v5 objects in 2.8, and a missing_genes parameter in 2.14 that lets callers impute or skip signature genes absent from the data. Version 2.16 tracks Bioconductor 3.23 and points at a new publication and a Python implementation, pyUCell.
Two threads run through this. The scoring algorithm itself has barely changed — the rank-based core is stable, and 2.14's reformatting to gene indices rather than string matching is a speed change, not a method change. What does change constantly is object-format compatibility, which is the tax of living between Seurat and SingleCellExperiment. The pyUCell reference in 2.16 is the first sign of the method reaching beyond R, though these notes say nothing about its scope.
The cadence is locked to Bioconductor's twice-yearly release train, so the next version will most likely accompany Bioconductor 3.24 with whatever Seurat or SingleCellExperiment changes it brings.
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 qtl2convert or UCell.
Pattern fills for ggplot2, hardened against the ways users write sizes
gcube's recent releases are all packaging metadata, not simulation code
The R port of Quinlan's Cubist gets reproducibility fixes, not new modelling
ggstats keeps widening what a coefficient or Likert plot can be
ecodive rebuilt itself into a broad diversity-metric library, breaking as it went
State-space data simulation for R, filled in one function at a time
See all qtl2convert alternatives → · See all UCell alternatives →
Latest ship moves from both products, interleaved chronologically. ⚡ = editorial spark.
Both compete on the same themes — r-package — within Analytics. qtl2convert and UCell are shipping at a similar cadence (velocity 0.0 vs 0.0, both within Sparkpulse's "active" band). 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. qtl2convert and UCell are shipping at a similar cadence (velocity 0.0 vs 0.0, both within Sparkpulse's "active" band). For your specific use case, the alternatives sections above list other Analytics products to evaluate alongside.
Top qtl2convert alternatives in Analytics are ranked by recent ship velocity. Browse the "qtl2convert alternatives" section above for the current picks, or visit /alternatives/qtl2convert for the full list with editorial commentary on each.
Top UCell alternatives in Analytics are ranked by recent ship velocity. Browse the "UCell alternatives" section above for the current picks, or visit /alternatives/ucell for the full list with editorial commentary on each.