Update README.md
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README.md
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@@ -20,29 +20,6 @@ task_categories:
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- other
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source_datasets:
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- original
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dataset_info:
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features:
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- name: regulator_locus_tag
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dtype: string
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description: Systematic gene name (ORF identifier) of the perturbed transcription factor
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- name: regulator_symbol
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dtype: string
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description: Standard gene symbol of the perturbed transcription factor
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- name: target_locus_tag
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dtype: string
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description: Systematic gene name (ORF identifier) of the target gene measured
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- name: target_symbol
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dtype: string
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description: Standard gene symbol of the target gene measured
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- name: dye_plus
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dtype: float
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description: Normalized log2 fold change for positive (+) dye orientation
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- name: dye_minus
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dtype: float
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description: Normalized log2 fold change for negative (-) dye orientation
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- name: mean_norm_log2fc
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dtype: float
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description: Average log2 fold change across dye orientations; 0 when orientations have opposite signs, single value when only one orientation available
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configs:
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- config_name: metadata
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description: Transcription factor metadata including essentiality and QC status
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@@ -50,16 +27,87 @@ configs:
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data_files:
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- split: train
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path: metadata.parquet
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- config_name: overexpression
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description: Overexpression perturbation normalized log2 fold changes
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data_files:
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- split: train
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path: overexpression.parquet
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- config_name: knockout
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description: Deletion/knockout perturbation normalized log2 fold changes
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data_files:
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- split: train
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path: knockout.parquet
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---
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# Hughes 2006
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@@ -101,4 +149,41 @@ BrentLab/yeast_genome_resources
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| `del_passed_qc` | Boolean indicating whether deletion experiments passed quality control |
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**Dataset Author and Contact**: Chase Mateusiak [@cmatKhan](https://github.com/cmatkhan/)
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- other
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source_datasets:
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- original
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configs:
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- config_name: metadata
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description: Transcription factor metadata including essentiality and QC status
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data_files:
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- split: train
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path: metadata.parquet
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+
dataset_info:
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+
features:
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+
- name: regulator_locus_tag
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+
dtype: string
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+
description: Systematic gene name (ORF identifier) of the transcription factor
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+
- name: regulator_symbol
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dtype: string
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description: Standard gene symbol of the transcription factor
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- name: found_domain
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dtype: string
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description: Identified DNA-binding domain(s) or protein family classification
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- name: sgd_description
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dtype: string
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description: Functional description from Saccharomyces Genome Database (SGD)
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- name: essential
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dtype: bool
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description: Boolean indicating whether the gene is essential for viability
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- name: oe_passed_qc
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dtype: bool
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description: Boolean indicating whether overexpression experiments passed quality control
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- name: del_passed_qc
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dtype: bool
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description: Boolean indicating whether deletion experiments passed quality control
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+
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- config_name: overexpression
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description: Overexpression perturbation normalized log2 fold changes
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data_files:
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- split: train
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path: overexpression.parquet
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+
dataset_info:
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+
features:
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+
- name: regulator_locus_tag
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+
dtype: string
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+
description: Systematic gene name (ORF identifier) of the perturbed transcription factor
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+
- name: regulator_symbol
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+
dtype: string
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+
description: Standard gene symbol of the perturbed transcription factor
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+
- name: target_locus_tag
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+
dtype: string
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+
description: Systematic gene name (ORF identifier) of the target gene measured
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+
- name: target_symbol
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+
dtype: string
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+
description: Standard gene symbol of the target gene measured
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+
- name: dye_plus
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+
dtype: float64
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description: Normalized log2 fold change for positive (+) dye orientation
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+
- name: dye_minus
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+
dtype: float64
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+
description: Normalized log2 fold change for negative (-) dye orientation
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+
- name: mean_norm_log2fc
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+
dtype: float64
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+
description: Average log2 fold change across dye orientations
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+
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- config_name: knockout
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description: Deletion/knockout perturbation normalized log2 fold changes
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data_files:
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- split: train
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path: knockout.parquet
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+
dataset_info:
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+
features:
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+
- name: regulator_locus_tag
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+
dtype: string
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+
description: Systematic gene name (ORF identifier) of the perturbed transcription factor
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+
- name: regulator_symbol
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+
dtype: string
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+
description: Standard gene symbol of the perturbed transcription factor
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+
- name: target_locus_tag
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+
dtype: string
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+
description: Systematic gene name (ORF identifier) of the target gene measured
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+
- name: target_symbol
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+
dtype: string
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+
description: Standard gene symbol of the target gene measured
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+
- name: dye_plus
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+
dtype: float64
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description: Normalized log2 fold change for positive (+) dye orientation
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+
- name: dye_minus
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+
dtype: float64
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+
description: Normalized log2 fold change for negative (-) dye orientation
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+
- name: mean_norm_log2fc
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+
dtype: float64
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description: Average log2 fold change across dye orientations
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---
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# Hughes 2006
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| `del_passed_qc` | Boolean indicating whether deletion experiments passed quality control |
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## Usage
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I recommend using `huggingface_hub.snapshot_download` to pull the repository. After that, use your favorite
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method of interacting with `parquet` files (eg duckDB, but you could use dplyr in R or pandas, too).
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```python
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from huggingface_hub import snapshot_download
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import duckdb
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import os
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repo_id = "BrentLab/hughes_2006"
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# Download entire repo to local directory
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repo_path = snapshot_download(
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repo_id=repo_id,
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repo_type="dataset"
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)
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print(f"Repository downloaded to: {repo_path}")
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# Construct path to the parquet file
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parquet_path = os.path.join(repo_path, "hughes_2006.parquet")
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print(f"Parquet file at: {parquet_path}")
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# Connect to DuckDB and query the parquet file
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conn = duckdb.connect()
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query = """
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SELECT *
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FROM read_parquet(?)
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WHERE regulator_locus_tag = 'YJR060W'
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"""
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result = conn.execute(query, [parquet_path]).fetchall()
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print(f"Found {len(result)} rows for YJR060W")
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```
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**Dataset Author and Contact**: Chase Mateusiak [@cmatKhan](https://github.com/cmatkhan/)
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