glyfun
glyfun is three releases old and has spent all of them chasing glyexp's container change.
A side-by-side editorial comparison of constants and glyenzy — release velocity, themes, recent moves, and the top alternatives to consider.
The R package for CODATA constants rebuilt its symbol table on NIST's naming so future updates stop being hand work.
constants exposes the CODATA recommended values of the physical constants to R, as a data frame plus symbol lists that carry units, uncertainties, or both. The package reached 1.0.0 on the 2018 CODATA release and has shipped once since, purely to track a units package update. Its surface is small and its release cadence is bound to CODATA, which revises every few years.
Glycan biosynthesis as a traceable enzyme graph, now including sulfation and gaps it can bridge.
glyenzy infers which enzymes could have produced a glycan and traces biosynthetic routes to it, backed by curated per-enzyme rules for human glycosyltransferases and, since 0.7.0, twelve sulfotransferases. Biosynthesis functions return typed network objects that keep their igraph interface while supporting layered DAG plots with glycan nodes and labelled enzyme edges. Where no concrete enzyme covers a step, bounded virtual transitions bridge the gap and are marked so users can see which edges are inferred rather than enzymatic.
constants exposes the CODATA recommended values of the physical constants to R, as a data frame plus symbol lists that carry units, uncertainties, or both. The package reached 1.0.0 on the 2018 CODATA release and has shipped once since, purely to track a units package update. Its surface is small and its release cadence is bound to CODATA, which revises every few years.
The direction set at 1.0.0 was to stop being a curated convenience wrapper and become a mechanical mirror of NIST. Hand-crafted symbol names were replaced with NIST's own ASCII symbols, categories adopted NIST's, and uncertainty switched from relative to absolute — all framed by the maintainer as necessary to make future CODATA updates routine. On top of that the package gained a correlation matrix and optional integration with the quantities package, moving it from a lookup table toward something that can propagate uncertainty.
Having rebuilt the symbol table specifically so CODATA revisions become mechanical, the next substantive release most likely tracks a new CODATA dataset rather than adding API. The experimental correlated-value support, disabled by default at 1.0.0, is the one part these entries flag as unfinished.
glyenzy infers which enzymes could have produced a glycan and traces biosynthetic routes to it, backed by curated per-enzyme rules for human glycosyltransferases and, since 0.7.0, twelve sulfotransferases. Biosynthesis functions return typed network objects that keep their igraph interface while supporting layered DAG plots with glycan nodes and labelled enzyme edges. Where no concrete enzyme covers a step, bounded virtual transitions bridge the gap and are marked so users can see which edges are inferred rather than enzymatic.
Two kinds of release alternate here. One is enzyme curation, a steady stream of rule corrections for the FUT, MAN1A and MGAT families and removals where an enzyme turned out to act only on glycolipids, which is the unglamorous accuracy work a rule-based inference engine lives on. The other is turning biosynthesis output into a first-class object: paths became networks, networks became typed with plotting support, and targets became a marked vertex attribute. The package moves in lockstep with its siblings, pinning glyrepr 0.13.0 and glymotif 0.17.0 as those refreshed their data and matching APIs, and the latest release already speaks glydraw 0.8.0's orientation values.
The paucimannose N-glycan support dropped in 0.7.0 is the obvious loose end, with users told to stay on 0.6.3, so a reinstated implementation is a plausible next move. Beyond that the virtual-step machinery is new enough that its heuristics, particularly the inferred step limits added in 0.8.1, should keep being tuned.
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 constants or glyenzy.
glyfun is three releases old and has spent all of them chasing glyexp's container change.
glydet is rebuilding its glycan trait vocabulary on top of someone else's container.
glyexp is retiring its own data container and handing the job to Bioconductor.
A glycan motif matcher trading convenience wrappers for speed, strictness and explicit specs.
The type system the rest of the glycan stack is built on, being hardened one breaking change at a time.
Glycan annotation stops depending on the database having seen the structure before.
See all constants alternatives → · See all glyenzy alternatives →
Latest ship moves from both products, interleaved chronologically. ⚡ = editorial spark.
They serve adjacent needs but don't currently overlap on shipped themes. glyenzy is currently shipping more aggressively (velocity 6.3 vs 0.0), with 1 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. glyenzy is currently shipping more aggressively (velocity 6.3 vs 0.0), with 1 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 constants alternatives in Analytics are ranked by recent ship velocity. Browse the "constants alternatives" section above for the current picks, or visit /alternatives/constants-r for the full list with editorial commentary on each.
Top glyenzy alternatives in Analytics are ranked by recent ship velocity. Browse the "glyenzy alternatives" section above for the current picks, or visit /alternatives/glyenzy for the full list with editorial commentary on each.