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Compare modelos biológicos, motores de docking y flujos computacionales lado a lado. Filtre por modelo de acceso, huella de cómputo y categoría para obtener una tabla de decisiones útil en menos de un minuto.
| Atributo | ＋ Añadir herramienta | |||
|---|---|---|---|---|
| Category | Genomics & Bioinformatics | Genomics & Bioinformatics | Genomics & Bioinformatics | — |
| Subcategory | Research AI Methods | Regulatory Genomics | Conventional or Statistical Baselines | — |
| Company | Research / method authors | Google DeepMind | Research / method authors | — |
| Access mode | Confirm distribution and exact release | Research code or publication | Confirm distribution and exact release | — |
| Licence conditions | NOT_INDEPENDENTLY_AUDITED | Check code and model weights separately | NOT_INDEPENDENTLY_AUDITED | — |
| Compute requirements | Version and data dependent | Check selected checkpoint and runtime; no GPU catalog recommendation | Version and data dependent | — |
| Biological application | No registrado | No registrado | No registrado | — |
| Research workflow | No registrado | No registrado | No registrado | — |
| Evidence level | PEER_REVIEWED_METHOD_OR_CONFERENCE | Peer-reviewed primary method | PEER_REVIEWED_METHOD_OR_CONFERENCE | — |
| Commercial eligibility | NOT_INDEPENDENTLY_AUDITED | Unknown, requires audit | NOT_INDEPENDENTLY_AUDITED | — |
| Price | Verify access and licence | Check selected model licence | Verify access and licence | — |
| Availability ⓘ | Method paper or official documentation | Public research method/code | Method paper or official documentation | — |
| Features | EVE scientific method, Protein family homolog alignment and compatible human missense variants, Evolutionary deep generative variant effect estimate | Predicts genomic regulatory tracks and predicted functional effects of noncoding DNA variants., Genomic regulatory track, sequence-variant contrast | bcftools scientific method, Reference genome with aligned short-read input and correct ploidy assumptions, VCF/BCF variant calls and variants QC operations | — |
| Entry type | Source-scoped research method | Research AI model / method | Classical/statistical scientific method | — |
| AI role | DEEP_LEARNING | Published biomedical AI method | NON_AI_STATISTICAL | — |
| Input data | Protein family homolog alignment and compatible human missense variants | DNA sequence interval; alleles and tissue/assay ontology | Reference genome with aligned short-read input and correct ploidy assumptions | — |
| Output data | Evolutionary deep generative variant effect estimate | Genomic regulatory track; sequence-variant contrast | VCF/BCF variant calls and variants QC operations | — |
| Validation | Published method scope; no independent BioAtlas execution or benchmark | Requires independent dataset-specific evaluation | Published method scope; no independent BioAtlas execution or benchmark | — |
| Type | No registrado | No registrado | No registrado | — |
| Intended use | No registrado | No registrado | No registrado | — |
| Compatibility | No registrado | No registrado | No registrado | — |