B08-TR06 · same_source_table
Benchmarking DNA foundation models for genomic and genetic tasks — Molecular functional or pathogenic variant interpretation
pathogenic versus common SNP
协议指纹
PF-v1-C1DFA26EE456C882E9662FAE
只有 metric 和 protocol-metric fingerprint 都明确选定后，页面才会加载结果分片。
- Split
- nested chromosome-based held-out test groups
- 聚合
- average held-out AUROC
- 外部数据
- model-specific pretraining allowed
- Ensemble / best-of-N
- single reported configuration · 1
- 关键未知字段
- cross-work compute/hardware equivalence
交互结果表
在同一指纹内筛选和比较
请选择 metric 和指纹。
前 50 个可排名结果
只显示当前指纹与筛选条件。
同口径并排
| 参与者 | 配置 | 分数 | 排名 | Claim |
|---|
| 比较 | 参与者 / 配置 | 分数 | 排名 | Baseline / claim | 证据与配置 |
|---|
完整协议字段
- canonical dataset ids
- NR
- data version
- publication release 2025
- label visibility
- test labels available only to evaluator/reporting authors
- input modality
- variant plus molecular context
- preprocessing
- reference/alternate embeddings and paper-defined classifier
- model selection rule
- paper-defined downstream model
- inference budget
- single model
- protocol completeness
- complete_for_same_table_comparison