Genome Understanding Evaluation (GUE)
28 datasets/tasks in the native packaging; mapped here to five task families.
- 协议
- 1
- 结果行
- 10
- 工作
- 1
2026-08-06 快照
查找公开数值结果或可审计缺口。结果行数不等于独立实验数。
47 / 47 个 benchmark
28 datasets/tasks in the native packaging; mapped here to five task families.
Eighteen downstream tasks are benchmark instances, not eighteen unique task families.
Human-genome tasks with biologically aligned splits; inspect each track for leakage controls.
Regulatory DNA evaluation across zero-shot, probing and fine-tuning regimes.
Framework and dataset suite; native task count follows current release documentation.
Widely reused classification datasets; simple random-style splits can inflate biological generalization.
Long-range genomic tasks; exact sequence length and cell-type packaging vary by track.
One-time benchmark study rather than a maintained benchmark suite.
Thirteen native tasks; some reuse OpenVaccine, Optimus and CRISPR datasets.
Board is public; DeepASmRNA and DeeReCT-PolyA/PAS are exposed as distinct tracks; verify exact release and frozen splits before comparative claims.
Three core tasks plus a task-family view of the ribozyme-assay subset; the subset track is separated from the aggregate DMS-effect track.
Four native study processes; the GTEx tissue-specific splicing evaluation is additionally mapped to the alternative-splicing task family without changing the native-task count.
Blind, rolling CASP-like assessment; puzzle count and target composition change by round.
First dedicated CASP RNA season; preserve target/category filters.
Includes RNA and nucleic-acid-containing targets; 42-target figure is reported for the richer RNA set in later assessment work.
High-throughput DMS/2A3 reactivity prediction; leaderboard is archived.
Same raw competition data is repackaged by several RNA benchmark suites.
Community-standard inverse-folding set; protocol differences across folding engines reduce comparability.
Focused benchmark for non-canonical RNA base pairs.
Only molecular and functional variant challenges are in scope; phenotype-from-exome and patient-level tasks are excluded.
Historic blinded TF–DNA specificity assessment.
Held-out cell types and chromosomes improve realism, but access is through Synapse.
Docking benchmark; target version, bound/unbound state and redundancy filters must be recorded.
Useful for binding and docking, but not a single standardized leaderboard.
Decoy construction and pocket redundancy are material evaluation choices.
Official repository lists 17 design tasks. The ribosomal-loading task is separated as 5′UTR/translation-control design; the remaining instances stay consolidated under cis-regulatory design.
Twelve curated ASO/siRNA/shRNA datasets with explicit split comparisons.
Seven RNA structure–function datasets; task-level splits and structural redundancy controls should be preserved.
Large-scale nucleotide fitness benchmark; verify repository release before production adoption.
Prospective promoter-expression prediction challenge with experimental readout; not counted as a sequence-generation benchmark.
External set of 125 nucleic-acid–ligand complexes; model-paper benchmark, not community suite.
Emerging benchmark for RNA–small-molecule interaction; check release artifacts and negative construction.
Meta-suite packaging RGB, BEACON, GUE, Genomic Benchmarks and PGB; native_task_count=5 suites, not the sum of their downstream tasks.
One-time model study spanning 15 named data packages; PrismNet is additionally stratified into 17 HeLa RBP assays.
Two time-separated competitions with hidden targets; submissions provide five candidate 3D structures and are evaluated best-of-five.
Adversarial robustness wrapper over eight GUE histone-mark datasets; four attack families and three defense strategies are evaluation regimes, not new biological task families.
Two released evaluation collections: CASP15 predicted models and Randstr decoys; benchmark package is fully archived on Zenodo.
Thirty-one chemical-mapping, riboswitch and external thermodynamic datasets; repository is archived but versioned and reproducible.
6,289 DNA/RNA aptamer–ligand records with fixed stratified, ligand-disjoint and aptamer-disjoint five-fold protocols; anonymous pre-review status should be preserved.
Manually confirmed interaction regions across archaea, bacteria and eukaryotes; the repository moved from UCanCompBio to Gardner-BinfLab.
Fixed generative riboswitch design evaluation over 685,109 unique sequences with validity and novelty metrics.
Evaluation against experimental-structure and molecular-dynamics DNA-shape labels; a reusable study protocol rather than a community leaderboard.
Blind and independent RNA–protein affinity tests; only RNA-side mutations are in scope. MS2, diverse-complex and PUM2 tests remain separate protocols.
100,000 generated 1,024-bp promoters evaluated with the Sei H3K4me3 activity oracle, MSE, KS and fluency; comparisons are restricted to the same source table.
Fixed tertiary-structure-to-sequence design evaluation released with code and benchmark data; computational structural recovery only unless separately validated.
Multi-objective mRNA design with prospective wet-lab measurements of stability, expression and immunogenicity; it must not be ranked with computational-only protocols.
Structure-guided light-up aptamer generation with prospective fluorescence validation; secondary mapping to tertiary RNA design is recorded separately.
没有符合当前筛选条件的 benchmark。