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End of preview. Expand in Data Studio

Extended-BioAgentBench

A growing benchmark for evaluating LLM agents on complex bioinformatics workflows.

Dataset on HF Tasks Based on

Building on BioAgentBench (10 tasks), this benchmark adds 71 new tasks that test LLM agents on increasingly complex, multi-tool bioinformatics pipelines. Tasks span 6 domains and range from simple linear workflows to depth-8 diamond DAGs with 16+ CLI tools.

This benchmark is actively growing — new tasks are added continuously to cover more domains, increase complexity, and push the boundaries of what AI agents can do in bioinformatics.

What makes this benchmark different?

  • Diamond DAG complexity: Tasks require running multiple independent tool branches that converge — not just linear pipelines
  • No pipeline leakage: Task prompts describe what to produce, never which tools to use or how to structure the pipeline
  • Domain-specific traps: Tasks include steps where default parameters silently produce wrong results (e.g., Tn5 shift correction in ATAC-seq, Medaka model selection for Nanopore)
  • Real public data: Every task uses published datasets with ground truth generated by validated reference pipelines

Tasks (71 total)

# Task ID Name
11 chipseq-peak-calling ChIP-seq Peak Calling: TAL1 Binding Site Comparison
12 bacterial-assembly Bacterial Genome Assembly and Annotation: MRSA Characte
13 mobile-elements Bacterial Mobile Genetic Element Characterization: MRSA
14 outbreak-investigation Foodborne Pathogen Outbreak Investigation via WGS Phylo
15 atacseq-accessibility ATAC-seq Chromatin Accessibility Profiling
16 longread-assembly Nanopore Long-read Bacterial Genome Assembly
17 hybrid-assembly Hybrid Genome Assembly from Illumina and Nanopore Data
18 sv-detection Bacterial Structural Variant and SNP Detection
19 pangenome-evolution E. coli Pan-genome and Core Phylogeny
20 metagenomic-profiling Metagenomic Assembly and Functional Profiling
21 phage-characterization Bacteriophage Genome Assembly and Functional Characteri
22 genome-comparison Pairwise Bacterial Genome Comparison
23 mapping-qc Genome Mapping and Coverage Quality Assessment
24 multisample-variants Multi-sample Variant Calling and Comparison
25 consensus-genome Bacterial Consensus Genome Generation
26 gene-prediction Gene Prediction Method Comparison
27 downsampling-analysis Read Downsampling and Assembly Quality Titration
28 plasmid-typing Plasmid Detection and Replicon Typing
29 genome-completeness Genome Completeness and Quality Assessment
30 species-identification Multi-reference Bacterial Species Identification
31 viral-amplicon Viral Amplicon Surveillance Analysis
32 bisulfite-methylation Bisulfite Sequencing DNA Methylation Analysis
33 rnaseq-isoform RNA-seq Isoform Assembly and Quantification
34 ancient-dna Ancient DNA Authentication and Damage Assessment
35 mirna-seq Small RNA-seq miRNA Discovery and Quantification
36 gcms-metabolomics GC-MS Metabolomics Profiling: Brown Algae Salinity Adap
37 cutandrun CUT&RUN Epigenomic Profiling
38 scrna-full-pipeline Single-Cell RNA-seq Full Pipeline: Multi-Quantifier Ana
39 crispr-screen CRISPR Screen Analysis: Drug Sensitivity Gene Discovery
40 amplicon-microbiome 16S Amplicon Microbiome: Community Profiling and Functi
41 rna-fusion RNA Fusion Detection from RNA-seq
42 spatial-transcriptomics Spatial Transcriptomics: Visium FFPE Brain Cancer Analy
43 taxonomic-profiling Multi-classifier Taxonomic Profiling of Metagenomic Rea
44 lcms-metabolomics LC-MS Untargeted Metabolomics: Urine Feature Discovery
45 somatic-variant-calling Somatic Variant Calling: Tumor-Normal Paired Analysis
46 amr-bgc-screening Antimicrobial Resistance and Biosynthetic Gene Cluster
47 variant-trio Variant Annotation Trio: Clinical Interpretation of Ash
48 clinical-metaproteomics Clinical Metaproteomics: Multi-Engine Marine Microbiome
49 mhc-immunopeptidomics MHC Immunopeptidomics: Peptide Identification and Quant
50 riboseq Ribosome Profiling Translation Analysis
51 neoantigen-prediction Neoantigen Prediction: Tumor-Normal Somatic Analysis
52 somatic-germline-dual Somatic+Germline Dual Analysis: Hereditary Cancer Varia
53 hicar-chromatin HiCAR Chromatin Interaction: Proximity Ligation and Acc
54 radseq-popgen RADseq Population Genetics: Stickleback Freshwater-Mari
55 mag-recovery MAG Recovery: Metagenome-Assembled Genomes from Environ
56 viral-phylodynamics Viral Phylodynamics (Molecular Clock Analysis)
57 edna-metabarcoding eDNA Aquatic Metabarcoding Biodiversity Assessment
58 metatranscriptomics Metatranscriptomics: Active Microbial Community Profili
59 nascent-transcription Nascent Transcription: GRO-seq Polymerase Activity Prof
60 circrna-discovery Circular RNA Discovery: C. elegans Wild-type vs fust-1
61 hic-3d-conformation Hi-C 3D Genome Conformation Analysis
62 genome-scaffolding Long-Read Genome Scaffolding of Fragmented Assembly
63 longread-rna-isoform Long-Read RNA Isoform Discovery from Direct RNA Sequenc
64 circrna-detection Circular RNA Detection and Quantification
65 pharmacogenomics CYP2D6 Pharmacogenomic Star Allele Calling
66 rna-editing-detection RNA Editing Detection: A-to-I Editing from Matched RNA/
67 cnv-detection-wes CNV Detection from Whole-Exome Sequencing
68 haplotype-phasing Haplotype Phasing and Genotype Refinement
69 dda-proteomics-simple DDA Proteomics: Single-Engine BSA Identification
70 immune-repertoire Immune Repertoire Analysis (BCR-seq)
71 germline-wes-gatk Germline WES Variant Calling: Clinical Exome Analysis
72 gwas-association GWAS Population Association Testing
73 dia-proteomics Label-Free Proteomics: BSA Standard Identification
74 structural-variant-multi Structural Variant Detection: Multi-caller Human SV Ana
75 dda-lfq-proteomics DDA Label-Free Quantitative Proteomics
76 clinical-wgs-interpretation Clinical WGS Interpretation: Full Clinical Genome Analy
77 repeat-element-annotation Repeat Element Annotation (Transposable Element Analysi
78 msi-detection Microsatellite Instability Detection: Multi-Caller Cons
79 scatac-seq Single-Cell ATAC-seq Chromatin Accessibility Analysis
80 multiomics-rna-atac Multi-omics Integration (RNA-seq + ATAC-seq)
81 methylation-array-epic Methylation Array Analysis (Illumina EPIC)

Quick start

# Clone and install
git clone https://github.com/lingzhi227/Extended-BioAgentBench.git
cd Extended-BioAgentBench
pip install click requests

# List tasks
python src/dataset.py list-tasks

# Download a specific task (data + reference + ground truth)
python src/dataset.py download --task outbreak-investigation --reference --results

# Download everything
python src/dataset.py download --all --reference --results

Task format

Each task follows the BioAgentBench format:

tasks/<task_id>/
  Dockerfile          # Reproduce ground truth with this
  environment.yml     # Conda environment specification
  run_script.sh       # Reference pipeline (ground truth generator)

Data, reference, and results are downloaded via dataset.py from HuggingFace:

tasks/<task_id>/
  data/               # Input data (FASTQ, FASTA, etc.)
  reference/          # Reference genomes (if needed)
  results/            # Ground truth output

Evaluation

Each task prompt provides the expected output format (CSV columns + example values). Evaluation uses GPT-5.1 as LLM-as-Judge, scoring:

  • steps_completed / steps_to_completion — how many pipeline stages the agent executed
  • completion_rate — fraction of the pipeline completed
  • results_match — full_match / partial_match / no_match against ground truth

Contributing new tasks

This benchmark is designed to grow. To add a new task:

  1. Pick a bioinformatics domain not yet covered
  2. Find small public data (< 1 GB, runtime < 4h on 8 CPUs)
  3. Write run_script.sh to generate ground truth
  4. Write a task prompt that says what to produce, not how
  5. Verify the prompt doesn't leak tool names or pipeline structure
  6. Submit a PR

Citation

Based on BioAgentBench:

@article{patino2025bioagentbench,
  title={BioAgentBench: A Benchmark for Evaluating LLM Agents in Bioinformatics},
  author={Patino, Luis and others},
  journal={arXiv preprint arXiv:2601.21800},
  year={2025}
}
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