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Comparison · Analytics

GeneNMF vs tbrf

A side-by-side editorial comparison of GeneNMF and tbrf — release velocity, themes, recent moves, and the top alternatives to consider.

Shared themes:r-package

GeneNMF vs tbrf: at a glance

FeatureGeneNMFtbrf
SectorAnalyticsAnalytics
Velocity score0.00.0
Sparks · 30d00
Top themessingle-cell-genomics, nmf, gene-programs, bioinformaticsrolling-statistics, water-quality, time-series, environmental-data
Last editorial update1h ago45m ago
WebsiteVisit →Visit →

What is GeneNMF?

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.

Read the full GeneNMF trajectory →

What is tbrf?

Time-based rolling statistics for water-quality data, finally getting plotting and padding built in.

tbrf computes rolling statistics over time windows rather than fixed row counts — geometric means, confidence intervals and related summaries indexed by date. That distinction matters for irregularly sampled environmental monitoring data, where a fixed-width window spans different amounts of real time. Version 0.1.7 folds in stat_stepribbon() from ggalt, ships an Entero example dataset for lognormal workflows, and adds na.pad across the tbr_ family.

Read the full tbrf trajectory →

GeneNMF vs tbrf: editorial side-by-side

G
GeneNMF
ANALYTICS
0.0

GeneNMF rebuilt how it derives meta-programs, changing every result it had produced.

◆ Current state

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.

◆ Where it's heading

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.

◆ Prediction

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.

T
tbrf
ANALYTICS
0.0

Time-based rolling statistics for water-quality data, finally getting plotting and padding built in.

◆ Current state

tbrf computes rolling statistics over time windows rather than fixed row counts — geometric means, confidence intervals and related summaries indexed by date. That distinction matters for irregularly sampled environmental monitoring data, where a fixed-width window spans different amounts of real time. Version 0.1.7 folds in stat_stepribbon() from ggalt, ships an Entero example dataset for lognormal workflows, and adds na.pad across the tbr_ family.

◆ Where it's heading

The package spent its middle releases absorbing upstream breakage — a lubridate duration redefinition, a tibble 3.0.0 subassignment change, tidyselect internals. The 0.1.7 release breaks that pattern: it is the first in five years to add capability rather than repair it, and it does so by internalising a stat from an abandoned dependency instead of relying on it. Cadence remains very low, with a five-year gap between 0.1.5 and 0.1.6.

◆ Prediction

Absorbing stat_stepribbon() directly suggests further vendoring of the plotting layer rather than new statistical functions. The entries do not indicate which rolling statistics, if any, are queued next.

Alternatives to GeneNMF and tbrf

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 GeneNMF or tbrf.

See all GeneNMF alternatives → · See all tbrf alternatives →

Recent activity from GeneNMF and tbrf

Latest ship moves from both products, interleaved chronologically. ⚡ = editorial spark.

  1. 11mo agoGeneNMFSingle-sample runs fixed; gene weight definition refined
  2. 0y agotbrfstat_stepribbon vendored in, plus na.pad on all rolling functions
  3. 1y agoGeneNMFMetaprogram composition exposed and custom signature DBs supported
  4. 1y agotbrfgm_mean_ci forwards na.rm and zero.propagate correctly
  5. 1y agoGeneNMFSimilarity heatmap downsampling and meta-program removal
  6. 2y agoGeneNMFMeta-programs rebuilt on gene weight vectors and cosine similarity
  7. 2y agoGeneNMFFirst stable release published to CRAN
  8. 6y agotbrfFix internals broken by tibble 3.0.0 subassignment
  9. 6y agotbrfDate windows recomputed with intervals and periods

Frequently asked questions

What is the difference between GeneNMF and tbrf?

Both compete on the same themes — r-package — within Analytics. GeneNMF and tbrf 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.

Is GeneNMF better than tbrf?

Sparkpulse doesn't pick a winner — we score release velocity, not feature parity. GeneNMF and tbrf 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.

What are the best alternatives to GeneNMF?

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.

What are the best alternatives to tbrf?

Top tbrf alternatives in Analytics are ranked by recent ship velocity. Browse the "tbrf alternatives" section above for the current picks, or visit /alternatives/tbrf for the full list with editorial commentary on each.