gps2gtfs
gps2gtfs spent a release making its docs stop describing functions it does not have.
A side-by-side editorial comparison of glyenzy and pedmut — release velocity, themes, recent moves, and the top alternatives to consider.
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.
pedmut turns awkward mutation models into ones the likelihood engine can actually handle.
pedmut builds and transforms the mutation models used in pedigree likelihood calculations. Its recent arc is a toolkit of model transformations: makeReversible() with three methods, makeStationary() replacing the older stabilize(), adjustRate() for tuning overall mutation rate, and lumpMutSpecial() for lumping models that strong lumpability cannot handle. The most recent release is narrow, adding a programmatic output format to getParams().
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.
pedmut builds and transforms the mutation models used in pedigree likelihood calculations. Its recent arc is a toolkit of model transformations: makeReversible() with three methods, makeStationary() replacing the older stabilize(), adjustRate() for tuning overall mutation rate, and lumpMutSpecial() for lumping models that strong lumpability cannot handle. The most recent release is narrow, adding a programmatic output format to getParams().
The consistent goal is making models satisfy the mathematical properties downstream algorithms require. Reversibility, stationarity, and lumpability each unlock something in pedprobr, and the package keeps adding ways to coerce an arbitrary model into having them. lumpMutSpecial() is explicitly incomplete, described as covering only some cases with more possibly to follow, which sets up the main open thread.
Expect additional special lumping cases to be implemented, since the package documents the current coverage as partial and pedprobr's likelihood performance depends directly on it.
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 glyenzy or pedmut.
gps2gtfs spent a release making its docs stop describing functions it does not have.
ducksemantics puts an ontology graph and ColBERT retrieval inside DuckDB, callable from R.
dvir keeps making disaster victim identification a single call instead of a workflow.
pedbuildr reconstructs pedigrees from DNA, and it just got much faster at the search.
forrel is getting faster at the simulations forensic kinship work actually spends its time on.
pedFamilias exists to read one legacy file format, and it has that job nearly finished.
See all glyenzy alternatives → · See all pedmut 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 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.
Top pedmut alternatives in Analytics are ranked by recent ship velocity. Browse the "pedmut alternatives" section above for the current picks, or visit /alternatives/pedmut for the full list with editorial commentary on each.