Datasets:
dataset card: Dataset Viewer configs (8 configs)
Browse files
README.md
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- zero-shot
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- protein-embeddings
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size_categories:
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---
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# AMBIMOD benchmark data (K562)
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Derived evaluation data for the AMBIMOD zero-shot perturbation-prediction
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benchmark.
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## Dataset Access
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This repository hosts the processed, benchmark-ready derived data (490-TF
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cohort, locked response matrices, protein embeddings, split manifests).
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- Norman 2019 CRISPRa (GEARS-official file, Harvard Dataverse): https://dataverse.harvard.edu/api/access/datafile/6154020
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```
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responses_doublet_filtered/
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responses_log1p_delta.npy # (490, 5, 1000) log1p-delta responses
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target_gene_indices.npy # 1000 target-gene indices
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metadata.json
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annotations/
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dbd_annotations_doublet_filtered.csv # DNA-binding-domain families
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ensembl_paralogs_doublet_filtered.json# paralog graph (leakage control)
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data/
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splits/
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k562/{design}_seed{NN}.json # 15 frozen split manifests (train/test TF lists)
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eligible_tfs.json, seed*.json # RPE1 frozen splits (raw-data pipeline)
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embedding_checksums.txt # SHA-256 of every embedding file
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download_*.sh # raw-data download scripts (optional rebuild)
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EMBEDDINGS.md # embedding provenance + reproduction guide
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```
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##
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All embedding caches were **computed by us** from public model weights applied
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to the cohort's UniProt-reviewed sequences — no third-party embedding files
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| Embedding | Checkpoint | Pooling |
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|---|---|---|
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`scripts/recompute_embeddings.py` in the code repository rebuilds any cache
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from these checkpoints and fails on checksum mismatch. The RPE1 patched
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ProTrek cache and its gated sanity receipt are documented in
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`EMBEDDINGS.md` in the code repository.
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## Usage
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```bash
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huggingface-cli download wozhen/ambimod --repo-type dataset --local-dir .
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tar xzf ambimod-benchmark-data.tar.gz
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pip install -e git+https://github.com/ambimod/ambimod#egg=ambimod
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python -c "from mechid.benchmark import load_benchmark; s = load_benchmark(); print(len(s))"
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# -> 15
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- zero-shot
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- protein-embeddings
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size_categories:
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- 1M<n<10M
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configs:
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- config_name: cohort
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data_files:
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- split: train
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path: viewer/cohort/*.parquet
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- config_name: annotations
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data_files:
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- split: train
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path: viewer/annotations/*.parquet
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- config_name: responses
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data_files:
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- split: train
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path: viewer/responses/*.parquet
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- config_name: embeddings_esm2_650m
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data_files:
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- split: train
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path: viewer/embeddings/embedding_esm2_650m.parquet
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- config_name: embeddings_esm2_3b
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data_files:
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- split: train
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path: viewer/embeddings/embedding_esm2_3b.parquet
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- config_name: embeddings_protrek
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data_files:
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- split: train
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path: viewer/embeddings/embedding_protrek.parquet
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- config_name: splits
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data_files:
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- split: train
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path: viewer/splits/splits.parquet
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- config_name: rpe1_splits
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data_files:
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- split: train
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path: viewer/splits/rpe1_splits.parquet
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---
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# AMBIMOD benchmark data (K562)
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Derived evaluation data for the AMBIMOD zero-shot perturbation-prediction
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benchmark. The data is organized into Dataset-Viewer configs (browse each
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tab above) plus a ready-to-use archive for the benchmark code.
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## Dataset Access
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Two equivalent access paths:
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**A. Load individual tables with `datasets`** (what the Dataset Viewer shows):
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```python
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from datasets import load_dataset
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cohort = load_dataset("wozhen/ambimod", "cohort", split="train")
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splits = load_dataset("wozhen/ambimod", "splits", split="train")
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responses = load_dataset("wozhen/ambimod", "responses", split="train")
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```
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**B. Download the benchmark archive** (exact layout the code expects —
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`cache/`, `data/splits/`, checksums):
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```bash
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huggingface-cli download wozhen/ambimod --repo-type dataset --local-dir .
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tar xzf ambimod-benchmark-data.tar.gz
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```
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## Configs (Dataset Viewer tabs)
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| Config | Rows | Columns | Content |
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| `cohort` | 490 | tf, n_cells, sequence_length, sequence, uniprot_header | quality-controlled K562 TF cohort (UniProt-reviewed human sequences) |
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| `annotations` | 490+490 | tf ↔ DBD family (InterPro); tf ↔ paralog list | leakage-control annotations |
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| `responses` | 2,450,000 | tf, replicate (1–5), gene_idx, gene_id, log1p_delta | held-out evaluation responses: log1p-delta per TF × replicate × 1,000 target genes |
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| `embeddings_esm2_650m` | 627,200 | tf, dim, value | ESM2-650M embeddings (490 × 1280, L2-normalized) |
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| `embeddings_esm2_3b` | 1,254,400 | tf, dim, value | ESM2-3B embeddings (490 × 2560) |
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| `embeddings_protrek` | 501,760 | tf, dim, value | ProTrek-650M embeddings (490 × 1024) |
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| `splits` | 7,350 | design, seed, role, tf | the 15 frozen K562 splits (random / dbd_family / embed_ball × 5 seeds), train/test membership |
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| `rpe1_splits` | 6,534 | seed, role, perturbation | frozen RPE1 split manifests (reference for the raw-data pipeline) |
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Embeddings are stored in long format (`tf, dim, value`) for Viewer
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compatibility; the benchmark archive (`ambimod-benchmark-data.tar.gz`)
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contains the same values as dense `(490, d)` float32 arrays.
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## Raw Data Sources
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- K562 GWPS + RPE1 essentialome (Perturb-seq): https://gwps.wi.mit.edu/
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- K562/RPE1 figshare mirror (RPE1 h5ad, direct download): https://figshare.com/ndownloader/files/42362275
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- Norman 2019 CRISPRa (GEARS-official file, Harvard Dataverse): https://dataverse.harvard.edu/api/access/datafile/6154020
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## Embedding provenance
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All embedding caches were **computed by us** from public model weights applied
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to the cohort's UniProt-reviewed sequences — no third-party embedding files
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| Embedding | Checkpoint | Pooling |
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| `esm2_650m` | `facebook/esm2_t33_650M_UR50D` | residue mean (1022-aa length-weighted chunks), L2-normalized |
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| `esm2_3b` | `facebook/esm2_t36_3B_UR50D` | same |
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| `protrek` | `westlake-repl/ProTrek_650M` | official `get_protein_repr` |
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`scripts/recompute_embeddings.py` in the code repository rebuilds any cache
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from these checkpoints and fails on checksum mismatch. The RPE1 patched
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ProTrek cache and its gated sanity receipt are documented in
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`EMBEDDINGS.md` in the code repository.
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## Usage with the benchmark code
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```bash
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pip install -e git+https://github.com/ambimod/ambimod#egg=ambimod
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python -c "from mechid.benchmark import load_benchmark; s = load_benchmark(); print(len(s))"
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# -> 15
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