otheropenml/181-yeastclassificationbioinformaticsmulticlasstabularbenchmarkuciopenmlimbalanced

Yeast Protein Localization

Free

Open dataset

Sample structure: 100 / 100
6 download links issued
Seller: DataBazaar
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Category
Other
Records
1,484 rows
Format
PARQUET
Update Frequency
Not documented
Collection Method
uploaded
PII
No flagged field names; not a privacy audit
File Size
~0.02 MB
Download links issued
6

Source, license and coverage

Supplier documentation. These claims are separate from the automated sample score. A listing edit date is not a data freshness date.

License
Public
Source / creator
openml: 181
Collection method
Features were computed by Paul Horton and Kenta Nakai using a combination of expert-designed signal sequence recognition methods (McGeoch's, von Heijne's), membrane-spanning region prediction (ALOM), and discriminant analysis over amino acid composition of relevant protein regions. The target localization labels were assigned based on then-current biological annotation. OpenML hosts the data unchanged in ARFF format.
Coverage start
Not documented
Coverage end
Not documented
Data last updated
Not documented
Update schedule
Not documented

Source documentation ↗

The dataset is heavily class-imbalanced (CYT and NUC dominate; ERL has only 5 instances). Features reflect 1990s-era bioinformatics signal-prediction methods and are not state-of-the-art relative to modern sequence-embedding approaches. Labels reflect biological knowledge as of 1996 and may not match current SGD annotations. Source does not document additional gaps; buyers should validate empirically for any non-benchmark use. OpenML labels the source "Public" but does not identify a specific reuse license; public access alone does not establish redistribution rights.

Sample structure score: 100 / 100

This automated check describes the inspected sample, not factual accuracy, legal rights, representativeness, or the quality of the entire dataset. It is not a customer rating.

Assessed 10 sample records (JSON) on 2026-10-09. All records in the provided sample were checked.

CheckPointsEvidence
Populated cells50 / 5090 of 90 top-level cells contain a value. Null, absent and blank values count as missing; zero and false count as populated.
Consistent value types30 / 3090 of 90 populated cells match their column's most common observed type. Types are inferred, not checked against real-world truth.
Consistent record shape20 / 2010 of 10 records have the expected fields. CSV/TSV use the header width; JSON uses the union of observed keys.
Field-level findings and improvements

Check missing cells and mixed types below. Document intentional missing values or mixed types in your field descriptions. Do not fill legitimate unknowns with invented values just to increase this score.

FieldMissing cellsMost common typeOther populated types
mcg0 / 10number0 / 10
gvh0 / 10number0 / 10
alm0 / 10number0 / 10
mit0 / 10number0 / 10
erl0 / 10number0 / 10
pox0 / 10number0 / 10
vac0 / 10number0 / 10
nuc0 / 10number0 / 10
class_protein_localization0 / 10string0 / 10
How the score is calculated, its limitations, and how to correct an assessment →

About this data

Multi-class classification benchmark predicting cellular localization sites of yeast proteins from 8 sequence-derived numeric features across 10 classes.

Retrieve with your agent or Python

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Download the Python example
python3 retrieve-dataset.py 2ab35349-0b96-4826-aadf-5d4f29eb2510 --output dataset.bin
Full supplier documentation
## Overview The Yeast dataset is a canonical multi-class classification benchmark from UCI, mirrored on OpenML as dataset 181. It contains 1,484 instances of Saccharomyces cerevisiae proteins, each described by 8 numeric features derived from amino acid sequence signals, with a target label indicating one of 10 cellular localization sites (CYT, NUC, MIT, ME3, ME2, ME1, EXC, VAC, POX, ERL). Format: ARFF. Time coverage: static, derived from sequences available circa 1996. ## Schema - mcg — numeric — McGeoch's method for signal sequence recognition - gvh — numeric — von Heijne's method for signal sequence recognition - alm — numeric — score from ALOM membrane-spanning region prediction - mit — numeric — score from discriminant analysis on amino acid content of N-terminal region of mitochondrial and non-mitochondrial proteins - erl — numeric — presence of HDEL substring (ER retention signal), binary-valued - pox — numeric — peroxisomal targeting signal in C-terminus - vac — numeric — score of discriminant analysis on amino acid content of vacuolar and extracellular proteins - nuc — numeric — score of discriminant analysis of nuclear localization signals of nuclear and non-nuclear proteins - class_protein_localization — nominal — target: one of 10 localization sites ## Sources - OpenML dataset 181 — https://www.openml.org/d/181 — Public Domain (CC0) - Originally from UCI Machine Learning Repository (Horton & Nakai, 1996) — https://archive.ics.uci.edu/ml/datasets/Yeast ## Methodology Features were computed by Paul Horton and Kenta Nakai using a combination of expert-designed signal sequence recognition methods (McGeoch's, von Heijne's), membrane-spanning region prediction (ALOM), and discriminant analysis over amino acid composition of relevant protein regions. The target localization labels were assigned based on then-current biological annotation. OpenML hosts the data unchanged in ARFF format. ## Known gaps & limitations The dataset is heavily class-imbalanced (CYT and NUC dominate; ERL has only 5 instances). Features reflect 1990s-era bioinformatics signal-prediction methods and are not state-of-the-art relative to modern sequence-embedding approaches. Labels reflect biological knowledge as of 1996 and may not match current SGD annotations. Source does not document additional gaps; buyers should validate empirically for any non-benchmark use. ## Intended use & out-of-scope - IS for: tabular ML benchmarking, multi-class classifier evaluation, imbalanced-classification studies, teaching examples, AutoML test suites. - NOT for: production protein-localization prediction (use modern sequence models), and not deduplicated against standard ML benchmark suites — leakage risk if used to train models evaluated on OpenML/UCI tabular benchmarks. Original supplier listing: Yeast Protein Localization (UCI/OpenML) Classic multi-class classification benchmark predicting cellular localization sites of yeast proteins from 8 sequence-derived numeric features. 1,484 instances, 10 classes.

Schema

NameTypeDescription
mcgDOUBLESignal sequence recognition score from McGeoch's method, range [0–1].
gvhDOUBLESignal sequence recognition score from von Heijne's method, range [0–1].
almDOUBLEALOM membrane-spanning region prediction score, range [0–1].
mitDOUBLEDiscriminant analysis score for mitochondrial targeting in N-terminal region, range [0–1].
erlDOUBLEBinary indicator of HDEL ER retention signal presence, 0 or 1.
poxDOUBLEPeroxisomal targeting signal score in C-terminus, range [0–1].
vacDOUBLEDiscriminant analysis score for vacuolar/extracellular targeting, range [0–1].
nucDOUBLEDiscriminant analysis score for nuclear localization signals, range [0–1].
class_protein_localizationVARCHARCellular localization site: CYT, NUC, MIT, ME3, ME2, ME1, EXC, VAC, POX, or ERL.

Sample Data

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Via MCP Server
# 1. Add to your agent's MCP config (claude_desktop_config.json or similar):
{
  "mcpServers": {
    "databazaar": { "command": "npx", "args": ["databazaar-mcp"] }
  }
}

# 2. Your agent can then call:
search_datasets({ query: "Yeast Protein Localization" })
// Found: 2ab35349-0b96-4826-aadf-5d4f29eb2510
get_download_url({ dataset_id: "2ab35349-0b96-4826-aadf-5d4f29eb2510" })  // free — sign in with MCP OAuth first
Via REST API
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