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Claude Skills by FreedomIntelligence
github.com/FreedomIntelligence741 skills2 installs1,922 views
- Tooluniverse Systems BiologyComprehensive systems biology and pathway analysis using multiple pathway databases (Reactome, KEGG, WikiPathways, Pathway Commons, BioModels). Performs pathway enrichment, protein-pathway mapping, keyword searches, and systems-level analysis. Use when analyzing gene sets, exploring biological pathways, or investigating systems-level biology.Votes: 0GitHub stars: 2,984
- Tooluniverse Target ResearchGather comprehensive biological target intelligence from 9 parallel research paths covering protein info, structure, interactions, pathways, expression, variants, drug interactions, and literature. Features collision-aware searches, evidence grading (T1-T4), explicit Open Targets coverage, and mandatory completeness auditing. Use when users ask about drug targets, proteins, genes, or need target validation, druggability assessment, or comprehensive target profiling.Votes: 0GitHub stars: 2,984
- Tooluniverse Variant AnalysisProduction-ready VCF processing, variant annotation, mutation analysis, and structural variant (SV/CNV) interpretation for bioinformatics questions. Parses VCF files (streaming, large files), classifies mutation types (missense, nonsense, synonymous, frameshift, splice, intronic, intergenic) and structural variants (deletions, duplications, inversions, translocations), applies VAF/depth/quality/consequence filters, annotates with ClinVar/dbSNP/gnomAD/CADD via ToolUniverse, interprets SV/CNV c...Votes: 0GitHub stars: 2,984
- Tooluniverse Variant InterpretationSystematic clinical variant interpretation from raw variant calls to ACMG-classified recommendations with structural impact analysis. Aggregates evidence from ClinVar, gnomAD, CIViC, UniProt, and PDB across ACMG criteria. Produces pathogenicity scores (0-100), clinical recommendations, and treatment implications. Use when interpreting genetic variants, classifying variants of uncertain significance (VUS), performing ACMG variant classification, or translating variant calls to clinical actiona...Votes: 0GitHub stars: 2,984
- Torch GeometricGraph Neural Networks (PyG). Node/graph classification, link prediction, GCN, GAT, GraphSAGE, heterogeneous graphs, molecular property prediction, for geometric deep learning.Votes: 0GitHub stars: 2,984
- TorchdrugGraph-based drug discovery toolkit. Molecular property prediction (ADMET), protein modeling, knowledge graph reasoning, molecular generation, retrosynthesis, GNNs (GIN, GAT, SchNet), 40+ datasets, for PyTorch-based ML on molecules, proteins, and biomedical graphs.Votes: 0GitHub stars: 2,984
- Tpd Ternary Complex Agent--> --- name: 'tpd-ternary-complex-agent' description: 'AI-powered ternary complex prediction for targeted protein degradation, modeling POI-degrader-E3 ligase assemblies to optimize PROTAC and molecular glue efficacy.' measurable_outcome: Execute skill workflow successfully with valid output within 15 minutes. allowed-tools: - read_file - run_shell_command --- The **TPD Ternary Complex Agent** specializes in predicting and modeling ternary complex formation for targeted protein degradation (...Votes: 0GitHub stars: 2,984
- TransformersThis skill should be used when working with pre-trained transformer models for natural language processing, computer vision, audio, or multimodal tasks. Use for text generation, classification, question answering, translation, summarization, image classification, object detection, speech recognition, and fine-tuning models on custom datasets.Votes: 0GitHub stars: 2,984
- Travel Health Analyzer分析旅行健康数据、评估目的地健康风险、提供疫苗接种建议、生成多语言紧急医疗信息卡片。支持WHO/CDC数据集成的专业级旅行健康风险评估。Votes: 0GitHub stars: 2,984
- Treatment PlansGenerate concise (3-4 page), focused medical treatment plans in LaTeX/PDF format for all clinical specialties. Supports general medical treatment, rehabilitation therapy, mental health care, chronic disease management, perioperative care, and pain management. Includes SMART goal frameworks, evidence-based interventions with minimal text citations, regulatory compliance (HIPAA), and professional formatting. Prioritizes brevity and clinical actionability.Votes: 0GitHub stars: 2,984
- Trial Eligibility Agent--> --- name: trial-eligibility-agent description: Parse trial protocols and patient data to produce criterion-level MET/NOT/UNKNOWN determinations with evidence and gaps for clinical trial screening tasks. allowed-tools: - read_file - run_shell_command ---Votes: 0GitHub stars: 2,984
- Trialgpt Matching--> --- name: trialgpt-matching description: Trial shortlist keywords: - retrieval - ranking - ClinicalTrials - patient-profile measurable_outcome: Produce ≥5 ranked trials (when available) with rationale + missing-data notes within 3 minutes of receiving a patient query. license: MIT metadata: author: TrialGPT Team version: "1.0.0" compatibility: - system: Python 3.9+ allowed-tools: - run_shell_command - read_file --- Run the locally checked-out TrialGPT pipeline to retrieve, rank, and expla...Votes: 0GitHub stars: 2,984
- Tumor Clonal Evolution Agent--> --- name: 'tumor-clonal-evolution-agent' description: 'AI-powered analysis of tumor clonal architecture, subclonal dynamics, and evolutionary trajectories from multi-region sequencing and longitudinal liquid biopsy data.' measurable_outcome: Execute skill workflow successfully with valid output within 15 minutes. allowed-tools: - read_file - run_shell_command --- The **Tumor Clonal Evolution Agent** analyzes intratumoral heterogeneity (ITH), reconstructs tumor phylogenies, and tracks clon...Votes: 0GitHub stars: 2,984
- Tumor Heterogeneity Agent--> --- name: 'tumor-heterogeneity-agent' description: 'AI-powered intratumor heterogeneity analysis for clonal architecture reconstruction, subclonal evolution tracking, and therapy resistance prediction using multi-region and longitudinal sequencing.' measurable_outcome: Execute skill workflow successfully with valid output within 15 minutes. allowed-tools: - read_file - run_shell_command --- The **Tumor Heterogeneity Agent** provides comprehensive analysis of intratumor heterogeneity (ITH)...Votes: 0GitHub stars: 2,984
- Tumor Mutational Burden Agent--> --- name: 'tumor-mutational-burden-agent' description: 'Calculates and harmonizes Tumor Mutational Burden (TMB) across platforms to predict immunotherapy response.' keywords: - tmb - immunotherapy - biomarker - harmonization - oncology measurable_outcome: 'Harmonizes TMB scores across 5+ assay platforms with <5% variance from WES gold standard.' allowed-tools: - read_file - run_shell_command --- The **Tumor Mutational Burden Agent** provides comprehensive TMB analysis for immunotherapy re...Votes: 0GitHub stars: 2,984
- Ukb NavigatorSemantic search across UK Biobank's 12,000+ data fields and publications — find the right variables for your research question.Votes: 0GitHub stars: 2,984
- Umap LearnUMAP dimensionality reduction. Fast nonlinear manifold learning for 2D/3D visualization, clustering preprocessing (HDBSCAN), supervised/parametric UMAP, for high-dimensional data.Votes: 0GitHub stars: 2,984
- Uniprot DatabaseDirect REST API access to UniProt. Protein searches, FASTA retrieval, ID mapping, Swiss-Prot/TrEMBL. For Python workflows with multiple databases, prefer bioservices (unified interface to 40+ services). Use this for direct HTTP/REST work or UniProt-specific control.Votes: 0GitHub stars: 2,984
- Universal Single Cell Annotator--> --- name: 'universal-single-cell-annotator' description: 'Annotate scRNA-seq' measurable_outcome: Execute skill workflow successfully with valid output within 15 minutes. allowed-tools: - read_file - run_shell_command --- This skill wraps multiple cell type annotation strategies into a single Python class. It allows agents to flexibly choose between rule-based (markers), data-driven (CellTypist), or reasoning-based (LLM) approaches depending on the context.Votes: 0GitHub stars: 2,984
- Using Git WorktreesUse when starting feature work that needs isolation from current workspace or before executing implementation plans - creates isolated git worktrees with smart directory selection and safety verificationVotes: 0GitHub stars: 2,984
- Using SuperpowersUse when starting any conversation - establishes how to find and use skills, requiring Skill tool invocation before ANY response including clarifying questionsVotes: 0GitHub stars: 2,984
- UsmlePrepare for US medical licensing exams with progress tracking, weak area analysis, question bank management, and residency match planning.Votes: 0GitHub stars: 2,984
- Uspto DatabaseAccess USPTO APIs for patent/trademark searches, examination history (PEDS), assignments, citations, office actions, TSDR, for IP analysis and prior art searches.Votes: 0GitHub stars: 2,984
- VaexUse this skill for processing and analyzing large tabular datasets (billions of rows) that exceed available RAM. Vaex excels at out-of-core DataFrame operations, lazy evaluation, fast aggregations, efficient visualization of big data, and machine learning on large datasets. Apply when users need to work with large CSV/HDF5/Arrow/Parquet files, perform fast statistics on massive datasets, create visualizations of big data, or build ML pipelines that do not fit in memory.Votes: 0GitHub stars: 2,984
- Varcadd Pathogenicity--> --- name: varcadd-pathogenicity description: Variant Scorer keywords: - variant-interpretation - CADD - pathogenicity - genomics - prediction measurable_outcome: Return pathogenicity scores for a VCF of 1000 variants within 2 minutes, flagging top 1% deleterious hits. license: Non-Commercial metadata: author: Genome Medicine 2025 version: "1.0.0" compatibility: - system: Python 3.9+ allowed-tools: - run_shell_command - read_file --- Genome-wide pathogenicity prediction leveraging standing...Votes: 0GitHub stars: 2,984
- Variant Interpretation Acmg--> --- name: 'variant-interpretation-acmg' description: 'Classifies genetic variants according to ACMG (American College of Medical Genetics) guidelines.' measurable_outcome: Execute skill workflow successfully with valid output within 15 minutes. allowed-tools: - read_file - run_shell_command --- The **Variant Interpretation Skill** automates the classification of genetic variants (Pathogenic, Benign, VUS) using a rules-based engine derived from ACMG guidelines.Votes: 0GitHub stars: 2,984
- Clinical Interpretation--> --- name: bio-variant-calling-clinical-interpretation description: Clinical variant interpretation using ClinVar, ACMG guidelines, and pathogenicity predictors. Prioritize variants for diagnostic and research applications. Use when interpreting clinical significance of variants. tool_type: mixed primary_tool: InterVar measurable_outcome: Execute skill workflow successfully with valid output within 15 minutes. allowed-tools: - read_file - run_shell_command --- Prioritize and interpret vari...Votes: 0GitHub stars: 2,984
- Consensus Sequences--> --- name: bio-consensus-sequences description: Generate consensus FASTA sequences by applying VCF variants to a reference using bcftools consensus. Use when creating sample-specific reference sequences or reconstructing haplotypes. tool_type: cli primary_tool: bcftools measurable_outcome: Execute skill workflow successfully with valid output within 15 minutes. allowed-tools: - read_file - run_shell_command --- Apply variants to reference FASTA using bcftools consensus.Votes: 0GitHub stars: 2,984
- Deepvariant--> --- name: bio-variant-calling-deepvariant description: Deep learning-based variant calling with Google DeepVariant. Provides high accuracy for germline SNPs and indels from Illumina, PacBio, and ONT data. Use when calling variants with DeepVariant deep learning caller. tool_type: cli primary_tool: DeepVariant measurable_outcome: Execute skill workflow successfully with valid output within 15 minutes. allowed-tools: - read_file - run_shell_command ---Votes: 0GitHub stars: 2,984
- Filtering Best Practices--> --- name: bio-variant-calling-filtering-best-practices description: Comprehensive variant filtering including GATK VQSR, hard filters, bcftools expressions, and quality metric interpretation for SNPs and indels. Use when filtering variants using GATK best practices. tool_type: mixed primary_tool: bcftools measurable_outcome: Execute skill workflow successfully with valid output within 15 minutes. allowed-tools: - read_file - run_shell_command ---Votes: 0GitHub stars: 2,984
- Gatk Variant Calling--> --- name: bio-gatk-variant-calling description: Variant calling with GATK HaplotypeCaller following best practices. Covers germline SNP/indel calling, GVCF workflow for cohorts, joint genotyping, and variant quality score recalibration (VQSR). Use when calling variants with GATK HaplotypeCaller. tool_type: cli primary_tool: gatk measurable_outcome: Execute skill workflow successfully with valid output within 15 minutes. allowed-tools: - read_file - run_shell_command --- GATK HaplotypeCall...Votes: 0GitHub stars: 2,984
- Joint Calling--> --- name: bio-variant-calling-joint-calling description: Joint genotype calling across multiple samples using GATK CombineGVCFs and GenotypeGVCFs. Essential for cohort studies, population genetics, and leveraging VQSR. Use when performing joint genotyping across multiple samples. tool_type: cli primary_tool: GATK measurable_outcome: Execute skill workflow successfully with valid output within 15 minutes. allowed-tools: - read_file - run_shell_command --- Call variants jointly across multi...Votes: 0GitHub stars: 2,984
- Structural Variant Calling--> --- name: bio-variant-calling-structural-variant-calling description: Call structural variants (SVs) from short-read sequencing using Manta, Delly, and LUMPY. Detects deletions, insertions, inversions, duplications, and translocations that are too large for standard SNV callers. Use when detecting structural variants from short-read data. tool_type: cli primary_tool: manta measurable_outcome: Execute skill workflow successfully with valid output within 15 minutes. allowed-tools: - read_fi...Votes: 0GitHub stars: 2,984
- Variant Annotation--> --- name: bio-variant-annotation description: Comprehensive variant annotation using bcftools annotate/csq, VEP, SnpEff, and ANNOVAR. Add database annotations, predict functional consequences, and assess clinical significance. Use when annotating variants with functional and clinical information. tool_type: mixed primary_tool: VEP measurable_outcome: Execute skill workflow successfully with valid output within 15 minutes. allowed-tools: - read_file - run_shell_command ---Votes: 0GitHub stars: 2,984
- Variant Calling--> --- name: bio-variant-calling description: Call SNPs and indels from aligned reads using bcftools mpileup and call. Use when detecting variants from BAM files or generating VCF from alignments. tool_type: cli primary_tool: bcftools measurable_outcome: Execute skill workflow successfully with valid output within 15 minutes. allowed-tools: - read_file - run_shell_command --- Call SNPs and indels from aligned reads using bcftools.Votes: 0GitHub stars: 2,984
- Variant Normalization--> --- name: bio-variant-normalization description: Normalize indel representation and split multiallelic variants using bcftools norm. Use when comparing variants from different callers or preparing VCF for downstream analysis. tool_type: cli primary_tool: bcftools measurable_outcome: Execute skill workflow successfully with valid output within 15 minutes. allowed-tools: - read_file - run_shell_command --- Left-align indels and split multiallelic sites using bcftools norm.Votes: 0GitHub stars: 2,984
- Vcf Basics--> --- name: bio-vcf-basics description: View, query, and understand VCF/BCF variant files using bcftools and cyvcf2. Use when inspecting variants, extracting specific fields, or understanding VCF format structure. tool_type: cli primary_tool: bcftools measurable_outcome: Execute skill workflow successfully with valid output within 15 minutes. allowed-tools: - read_file - run_shell_command --- View and query variant files using bcftools and cyvcf2.Votes: 0GitHub stars: 2,984
- Vcf Manipulation--> --- name: bio-vcf-manipulation description: Merge, concatenate, sort, intersect, and subset VCF files using bcftools. Use when combining variant files, comparing call sets, or restructuring VCF data. tool_type: cli primary_tool: bcftools measurable_outcome: Execute skill workflow successfully with valid output within 15 minutes. allowed-tools: - read_file - run_shell_command --- Merge, concat, sort, and compare VCF files using bcftools.Votes: 0GitHub stars: 2,984
- Vcf Statistics--> --- name: bio-vcf-statistics description: Generate variant statistics, sample concordance, and quality metrics using bcftools stats and gtcheck. Use when evaluating variant quality, comparing samples, or summarizing VCF contents. tool_type: cli primary_tool: bcftools measurable_outcome: Execute skill workflow successfully with valid output within 15 minutes. allowed-tools: - read_file - run_shell_command --- Generate statistics and quality metrics using bcftools.Votes: 0GitHub stars: 2,984
- VarCADD--> --- name: varcadd-pathogenicity description: Variant Scorer keywords: - variant-interpretation - CADD - pathogenicity - genomics - prediction measurable_outcome: Return pathogenicity scores for a VCF of 1000 variants within 2 minutes, flagging top 1% deleterious hits. license: Non-Commercial metadata: author: Genome Medicine 2025 version: "1.0.0" compatibility: - system: Python 3.9+ allowed-tools: - run_shell_command - read_file --- Genome-wide pathogenicity prediction leveraging standing...Votes: 0GitHub stars: 2,984
- Vcf AnnotatorAnnotate VCF variants with VEP, ClinVar, gnomAD frequencies, and ancestry-aware context. Generates prioritised variant reports.Votes: 0GitHub stars: 2,984
- Verification Before CompletionUse when about to claim work is complete, fixed, or passing, before committing or creating PRs - requires running verification commands and confirming output before making any success claims; evidence before assertions alwaysVotes: 0GitHub stars: 2,984
- Virtual Lab Agent--> --- name: 'virtual-lab-agent' description: 'AI-powered virtual laboratory orchestrating multi-agent scientific research teams for autonomous hypothesis generation, experimental design, and validation in biomedical research.' measurable_outcome: Execute skill workflow successfully with valid output within 15 minutes. allowed-tools: - read_file - run_shell_command --- The **Virtual Lab Agent** orchestrates AI-powered virtual scientific research teams consisting of specialized agents (Princi...Votes: 0GitHub stars: 2,984
- Wearable Analysis Agent--> --- name: wearable-analysis-agent description: Analyzes longitudinal wearable sensor data (heart rate, activity, sleep) to detect anomalies and provide personalized health insights. keywords: - wearable - sensor-data - health-monitoring - anomaly-detection - longitudinal-analysis measurable_outcome: Detects atrial fibrillation and sleep anomalies with >90% accuracy using continuous PPG and accelerometer data. license: MIT metadata: author: Biomedical AI Team version: "1.0.0" compatibility...Votes: 0GitHub stars: 2,984
- Weightloss Analyzer分析减肥数据、计算代谢率、追踪能量缺口、管理减肥阶段Votes: 0GitHub stars: 2,984
- Wellally TechIntegrate digital health data sources (Apple Health, Fitbit, Oura Ring) and connect to WellAlly.tech knowledge base. Import external health device data, standardize to local format, and recommend relevant WellAlly.tech knowledge base articles based on health data. Support generic CSV/JSON import, provide intelligent article recommendations, and help users better manage personal health data.Votes: 0GitHub stars: 2,984
- Wikipedia SearchSearch and fetch structured content from Wikipedia using the MediaWiki API for reliable, encyclopedic informationVotes: 0GitHub stars: 2,984
- Writing PlansUse when you have a spec or requirements for a multi-step task, before touching codeVotes: 0GitHub stars: 2,984
- Writing SkillsUse when creating new skills, editing existing skills, or verifying skills work before deploymentVotes: 0GitHub stars: 2,984
- Xlsx OfficialComprehensive spreadsheet creation, editing, and analysis with support for formulas, formatting, data analysis, and visualization. When Claude needs to work with spreadsheets (.xlsx, .xlsm, .csv, .tsv, etc) for: (1) Creating new spreadsheets with formulas and formatting, (2) Reading or analyzing data, (3) Modify existing spreadsheets while preserving formulas, (4) Data analysis and visualization in spreadsheets, or (5) Recalculating formulasVotes: 0GitHub stars: 2,984