Datasets:
Add Malinois MPRA dataset card
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README.md
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dtype: string
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- name: variant_class
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dtype: string
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- name: sequence
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dtype: string
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- name: sequence_length
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dtype: int32
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- name: reverse_complement
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dtype: string
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- name: forward_rc_concat
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dtype: string
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- name: K562_log2FC
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dtype: float32
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- name: HepG2_log2FC
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dtype: float32
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- name: SKNSH_log2FC
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dtype: float32
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- name: K562_lfcSE
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dtype: float32
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- name: HepG2_lfcSE
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dtype: float32
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- name: SKNSH_lfcSE
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dtype: float32
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- name: K562_log2FC_train_zscore
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dtype: float32
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- name: HepG2_log2FC_train_zscore
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dtype: float32
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- name: SKNSH_log2FC_train_zscore
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dtype: float32
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- name: all_se_le_1
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dtype: bool
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- name: any_log2fc_gt_0_5
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dtype: bool
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splits:
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- name: train
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num_bytes: 627457079
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num_examples: 668946
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- name: validation
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num_bytes: 58894846
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num_examples: 62406
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- name: test
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num_bytes: 62485771
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num_examples: 66712
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download_size: 256932482
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dataset_size: 748837696
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configs:
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- config_name: default
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data_files:
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- split: train
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path: data/train-*
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- split: validation
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path: data/validation-*
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- split: test
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path: data/test-*
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---
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---
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pretty_name: Malinois/Gosai MPRA Regression
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task_categories:
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- tabular-regression
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tags:
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- biology
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- genomics
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- dna
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- mpra
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- carbon
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size_categories:
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- 100K<n<1M
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---
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# Malinois/Gosai MPRA Regression
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This dataset preprocesses the Gosai et al. 2024 supplementary MPRA table used by the
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Malinois benchmark for supervised DNA-to-activity regression. Each row contains a DNA
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sequence and three cell-type-specific activity targets: `K562_log2FC`,
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`HepG2_log2FC`, and `SKNSH_log2FC`.
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No new license is asserted by this preprocessing. Users should follow the terms of
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the source publication and supplementary data.
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## Source
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- Publication: Gosai et al., *Machine-guided design of cell-type-targeting
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cis-regulatory elements*, Nature 2024.
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- Source table: `41586_2024_8070_MOESM4_ESM.txt`.
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- Source URL: `https://static-content.springer.com/esm/art%3A10.1038%2Fs41586-024-08070-z/MediaObjects/41586_2024_8070_MOESM4_ESM.txt`.
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## Splits
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Chromosome splits match the Carbon fine-tuning experiments and the public Malinois
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setup we used:
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| Split | Chromosomes | Rows | Rows with all SE <= 1.0 |
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|---|---:|---:|---:|
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| train | all except validation/test chromosomes | 668,946 | 627,661 |
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| validation | 19, 21, X | 62,406 | 58,811 |
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| test | 7, 13 | 66,712 | 62,582 |
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Total rows after filtering finite targets/standard errors and nonempty sequences:
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798,064.
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## Columns
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- `id`: original row identifier from the source table.
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- `split`: train, validation, or test.
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- `chromosome`: normalized chromosome label.
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- `data_project`, `oligo`, `variant_class`: source metadata.
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- `sequence`: uppercase DNA sequence.
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- `reverse_complement`: reverse complement of `sequence`.
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- `forward_rc_concat`: `<dna>sequence</dna><dna>reverse_complement</dna>`,
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matching the best Carbon fine-tuning recipe.
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- `K562_log2FC`, `HepG2_log2FC`, `SKNSH_log2FC`: raw regression targets.
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- `K562_lfcSE`, `HepG2_lfcSE`, `SKNSH_lfcSE`: target standard errors.
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- `*_train_zscore`: target standardized using train-split mean/std.
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- `all_se_le_1`: true when all three SE columns are `<= 1.0`; this was the
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main reported validation/test metric filter.
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- `any_log2fc_gt_0_5`: true when any target is greater than `0.5`; this was used
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for optional high-activity training upsampling.
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Train z-score statistics:
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| Target | Mean | Std |
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|---|---:|---:|
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| K562_log2FC | 0.49943020 | 1.17725282 |
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| HepG2_log2FC | 0.46267671 | 1.05124023 |
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| SKNSH_log2FC | 0.41405871 | 1.16609108 |
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## Usage
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```py
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from datasets import load_dataset
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ds = load_dataset("edbeeching/malinois-mpra-regression")
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train = ds["train"]
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validation_metric = ds["validation"].filter(lambda row: row["all_se_le_1"])
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example = train[0]
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sequence = example["forward_rc_concat"]
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labels = [
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example["K562_log2FC_train_zscore"],
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example["HepG2_log2FC_train_zscore"],
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example["SKNSH_log2FC_train_zscore"],
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]
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```
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To recreate the dataset:
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```sh
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python create_dataset.py --repo-id edbeeching/malinois-mpra-regression --push
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```
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