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- ▌ Claude Agent System Instructions 3 · tools-only bundleYou are a deep research and scientific writing assistant that combines AI-driven research with well-formatted written outputs.
- ▌ Claude Agent System Instructions 4 · tools-only bundleYou are a deep research and scientific writing assistant that combines AI-driven research with well-formatted written outputs.
- ▌ Asset Patterns Reference · tools-only bundleOnce you've defined assets, use the dg launch command to materialize them. For comprehensive documentation on launching assets, see the CLI launch reference.
- ▌ Asset Patterns Reference 2 · tools-only bundleOnce you've defined assets, you'll need to materialize (launch) them. Use the modern dg launch command for all asset execution.
- ▌ Intelligent Scaffolding · tools-only bundleI'll create complete feature structures based on your project patterns, with full continuity across sessions.
- ▌ Integration Scaffolding · tools-only bundleInvoke the /dagster-integrations skill to help find an existing integration component that matches the user's use case.
- ▌ Exceptions Module · tools-only bundleDefines a custom exception hierarchy for structured error handling throughout TunaCode.
- ▌ Kraken2 Classification Usage Guide · tools-only bundleKraken2 is a fast taxonomic classifier that uses exact k-mer matches to assign reads to taxonomic nodes. It's highly accurate for well-represented taxa and ideal for screening large datasets.
- ▌ Cross Validation Usage Guide · tools-only bundleImplement proper cross-validation strategies to get unbiased performance estimates on biomedical datasets and avoid overfitting during biomarker discovery.
- ▌ Figure Export Usage Guide · tools-only bundleThis guide covers exporting publication-ready figures with proper resolution, sizing, and formatting.
- ▌ Functional Prediction Usage Guide · tools-only bundlePICRUSt2 predicts metagenome functional content from 16S/18S marker gene data by inferring gene content from phylogenetically related reference genomes.
- ▌ Local Blast Usage Guide · tools-only bundleThis skill enables AI agents to help you run BLAST searches locally using BLAST+ command-line tools, enabling fast unlimited searches against custom or downloaded databases.
- ▌ Fcs Handling Usage Guide · tools-only bundleFCS (Flow Cytometry Standard) is the standard file format for cytometry data. flowCore provides comprehensive tools for reading, writing, and manipulating FCS files.
- ▌ Bowtie2 Alignment Usage Guide · tools-only bundleBowtie2 is a fast and memory-efficient aligner for short reads. It supports both end-to-end and local alignment modes, making it versatile for ChIP-seq, ATAC-seq, and general short-read alignment.
- ▌ Mageck Analysis Usage Guide · tools-only bundleMAGeCK is the standard tool for analyzing pooled CRISPR screens. It handles count normalization, identifies significantly enriched/depleted genes, and performs pathway analysis.
- ▌ Hit Calling Usage Guide · tools-only bundleMultiple methods exist for calling hits in CRISPR screens. The choice depends on screen design, reference data availability, and desired stringency.
- ▌ Vcf Manipulation Usage Guide · tools-only bundleThis guide covers merging, concatenating, sorting, and comparing VCF files.
- ▌ Mirdeep2 Analysis Usage Guide · tools-only bundleDiscover novel miRNAs and quantify known miRNAs using miRDeep2's de novo prediction algorithm based on secondary structure and read patterns.
- ▌ Star Rna Seq Alignment Usage Guide · tools-only bundleSTAR (Spliced Transcripts Alignment to a Reference) is the most widely used RNA-seq aligner. It's extremely fast, supports splice-aware alignment, and can detect novel junctions with two-pass mode.
- ▌ Pileup Generation Usage Guide · tools-only bundleGenerate pileup data showing all reads covering each genomic position for variant calling and position-level analysis.
- ▌ Taxonomy Assignment Usage Guide · tools-only bundleTaxonomic assignment classifies ASVs or OTUs to taxonomic ranks (Kingdom through Species) using reference databases like SILVA, GTDB, or UNITE.
- ▌ Proximity Operations Usage Guide · tools-only bundleProximity operations help you find relationships between genomic features based on their distance.
- ▌ Iso Seq Analysis Usage Guide · tools-only bundleProcess PacBio Iso-Seq data for full-length transcript discovery and isoform characterization.
- ▌ Genotype Imputation Usage Guide · tools-only bundleGenotype imputation predicts untyped variants using haplotype patterns from a reference panel, enabling increased variant density for GWAS, fine-mapping, and polygenic risk score calculation.
- ▌ Alerting Integrations · tools-only bundleNotification and alerting systems for pipeline monitoring, team communication, and incident management.
- ▌ Alerting Webhooks · tools-only bundleimport Image from '@theme/IdealImage'; import Tabs from '@theme/Tabs'; import TabItem from '@theme/TabItem';
- ▌ Alerting API Reference · tools-only bundleComplete reference for Grafana Alerting HTTP API endpoints (Grafana 9.0+).
- ▌ Decision Checklists Reference · tools-only bundleIf any answer is "yes", wrap in a @cache-decorated function instead.
- ▌ Type Annotations Python 3 11 · tools-only bundleThis document provides complete, canonical type annotation guidance for Python 3.11.
- ▌ Type Annotations Python 3 13 · tools-only bundleThis document provides complete, canonical type annotation guidance for Python 3.13. Python 3.13 implements PEP 649 (Deferred Evaluation of Annotations), fundamentally changing how annotations are evaluated.
- ▌ API Design Reference · tools-only bundleboilerplate are explicitly exempt. These helpers often wrap complex constructors (like formatplanheader_body) with sensible defaults, and having many default parameters is their intended purpose—not a code smell
- ▌ MCP Overview 4 · tools-only bundleimport Tabs from '@theme/Tabs'; import TabItem from '@theme/TabItem'; import Image from '@theme/IdealImage';
- ▌ Ribosome Stalling Usage Guide · tools-only bundleDetect ribosome pausing and stalling sites at codon resolution to study translational regulation, rare codon effects, and nascent chain interactions.
- ▌ Type Annotations Python 3 12 · tools-only bundleThis document provides complete, canonical type annotation guidance for Python 3.12.
- ▌ Figlet Text Converter Usage Guide · tools-only bundleThe Figlet Text Converter skill converts marked text in files to ASCII art. It uses a universal tag syntax that works across all file types and intelligently preserves comment formatting.
- ▌ Entrez Link Usage Guide · tools-only bundleThis skill enables AI agents to help you navigate between NCBI databases, finding related records across different data types (genes, proteins, sequences, publications).
- ▌ Atac Seq Peak Calling Usage Guide · tools-only bundleCall accessible chromatin regions from ATAC-seq data using MACS3 or Genrich, with specialized handling for Tn5 transposase cut sites and nucleosome-free region detection.
- ▌ Structure Navigation Usage Guide · tools-only bundleThis skill covers navigating the SMCRA (Structure-Model-Chain-Residue-Atom) hierarchy in Biopython Bio.PDB.
- ▌ Functional Profiling Usage Guide · tools-only bundleHUMAnN3 profiles the functional potential of metagenomic communities by quantifying gene families (UniRef90) and inferring pathway abundances (MetaCyc).
- ▌ Pairwise Alignment Usage Guide · tools-only bundleThis skill performs pairwise sequence alignment to compare two DNA, RNA, or protein sequences. It uses Biopython's PairwiseAligner class which implements dynamic programming algorithms for finding optimal alignments.
- ▌ Lineage Tracing Analysis Usage Guide · tools-only bundleReconstruct cell lineage trees from CRISPR barcodes, mitochondrial mutations, or other heritable markers.
- ▌ Chip Seq Qc Usage Guide · tools-only bundleQuality control metrics for ChIP-seq experiments including FRiP, NSC/RSC, IDR, and library complexity measurements to assess enrichment quality and replicate reproducibility.
- ▌ Dg Scaffold Create Definitions · tools-only bundleScaffold Dagster definitions including Python objects (assets, schedules, sensors) and integration components.
- ▌ Dg Scaffold Create Definitions 2 · tools-only bundleScaffold Dagster definitions including Python objects (assets, schedules, sensors) and integration components.
- ▌ Alignment Indexing Usage Guide · tools-only bundleCreate and use indices for random access to BAM and CRAM files, enabling fast region queries without reading entire files.
- ▌ Qpcr Primer And Probe Design Usage Guide · tools-only bundleThis skill covers designing primers and probes for quantitative PCR (real-time PCR) using primer3-py. Supports TaqMan hydrolysis probes and SYBR Green primer-only assays.
- ▌ Adapter Trimming Usage Guide · tools-only bundleSequencing adapters must be removed before alignment to prevent misalignment and artifacts.
- ▌ Hisat2 Rna Seq Alignment Usage Guide · tools-only bundleHISAT2 is a memory-efficient splice-aware aligner for RNA-seq data. It uses a graph-based index that enables fast alignment with low memory usage (~8GB for human genome vs ~30GB for STAR).
- ▌ Differential Splicing Usage Guide · tools-only bundleDetect differential alternative splicing between experimental conditions. Identifies splicing events that change significantly between groups, reporting both statistical significance and effect size (delta PSI).
- ▌ Mofa2 Integration Usage Guide · tools-only bundleMOFA2 (Multi-Omics Factor Analysis v2) is an unsupervised method for integrating multiple omics layers. It decomposes the data into latent factors that explain shared and view-specific variation.
- ▌ Heatmaps And Clustering Usage Guide · tools-only bundleClustered heatmaps visualize matrix data (expression, methylation, etc.) with hierarchical clustering to reveal patterns across samples and features.
- ▌ Atac Seq Qc Usage Guide · tools-only bundleAssess ATAC-seq library quality using TSS enrichment, FRiP scores, fragment size distributions, mitochondrial contamination, and library complexity metrics.
- ▌ Pathway Mapping Usage Guide · tools-only bundlePathway mapping places differential metabolites in biological context, identifying affected metabolic processes using enrichment analysis and pathway topology.
- ▌ Classification Models Usage Guide · tools-only bundleBuild classification models for biomarker discovery and diagnostics using RandomForest, XGBoost, and logistic regression with sklearn-compatible APIs.
- ▌ Entrez Search Usage Guide · tools-only bundleThis skill enables AI agents to help you search NCBI databases using Biopython's Entrez module. It covers keyword searches, database exploration, and query building.
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- ▌ Scenic Regulons Usage Guide · tools-only bundleInfer transcription factor regulons from single-cell RNA-seq data using the pySCENIC three-step pipeline.
- ▌ Sashimi Plots Usage Guide · tools-only bundleCreate sashimi plots to visualize splicing events with read coverage and splice junction counts.
- ▌ Sparse Matrix Handling Usage Guide · tools-only bundleWork with sparse matrices (CSR, CSC, COO) for memory-efficient storage and operations on count data with many zero values, especially single-cell RNA-seq data.
- ▌ Repertoire Visualization Usage Guide · tools-only bundleCreate publication-quality visualizations of immune repertoire data including V-J circos plots, clone tracking, diversity comparisons, and clonotype networks.
- ▌ Metagenome Visualization Usage Guide · tools-only bundleVisualize and statistically analyze metagenomic profiles using Python (matplotlib, seaborn, scikit-learn) or R (phyloseq, vegan, ggplot2).
- ▌ Targeted Metabolomics Usage Guide · tools-only bundleTargeted metabolomics quantifies a predefined set of metabolites using selected reaction monitoring (SRM/MRM). This approach provides absolute quantification with high sensitivity and reproducibility.
- ▌ Secondary Structure Prediction Usage Guide · tools-only bundlePredict RNA secondary structures from sequence using thermodynamic models. ViennaRNA computes minimum free energy (MFE) structures, partition function ensembles, base-pair probabilities, consensus structures from…
- ▌ Interaction Databases Usage Guide · tools-only bundleThis skill enables AI agents to query protein-protein interaction (PPI) databases including STRING, BioGRID, IntAct, and OmniPath.
- ▌ Upset Plots Usage Guide · tools-only bundleUpSet plots visualize set intersections more effectively than Venn diagrams, especially for 4+ sets. They show intersection sizes as bar charts with a matrix indicating which sets participate.
- ▌ Time Series De Usage Guide · tools-only bundleIdentify genes with significant temporal expression patterns across time-course experiments using spline models, polynomial regression, or likelihood ratio tests.
- ▌ Multiomics Grn Inference Usage Guide · tools-only bundleBuild enhancer-driven gene regulatory networks by integrating single-cell RNA-seq and ATAC-seq data.
- ▌ Alignment Statistics Usage Guide · tools-only bundleGenerate QC statistics from alignment files including mapping rates, read counts, coverage depth, and per-chromosome distributions.
- ▌ Quarto Reports Usage Guide · tools-only bundleQuarto is a next-generation scientific publishing system supporting R, Python, Julia, and Observable with enhanced features over R Markdown.
- ▌ Uniprot Access Usage Guide · tools-only bundleThis skill enables AI agents to help you query UniProt programmatically using the REST API to retrieve protein sequences, annotations, and functional information.
- ▌ Dbsnp Queries Usage Guide · tools-only bundleQuery dbSNP for rsID lookups, coordinate mapping, and variant annotations using myvariant.info or NCBI Entrez APIs.
- ▌ Cnv Annotation Usage Guide · tools-only bundleCNV annotation adds biological context to copy number calls by identifying affected genes, pathways, and clinical significance. This is essential for interpreting CNV findings in research and clinical contexts.
- ▌ Scaffolding Usage Guide · tools-only bundleScaffolding orders and orients contigs into chromosome-level assemblies using Hi-C proximity ligation data to infer long-range contacts.
- ▌ Flow Cytometry Pipeline Usage Guide · tools-only bundleThis workflow processes flow cytometry data from raw FCS files through compensation, transformation, clustering or gating, and differential analysis.
- ▌ Ggplot2 Fundamentals Usage Guide · tools-only bundleggplot2 is a declarative visualization system based on the Grammar of Graphics. Build publication-quality figures layer by layer.
- ▌ Conservation Genetics Usage Guide · tools-only bundleAssesses the genetic health of populations for conservation management. Covers F-statistics and genetic diversity metrics (hierfstat), allelic richness, pairwise population differentiation, runs of homozygosity for…
- ▌ Circadian Rhythm Detection Usage Guide · tools-only bundleDetects circadian and ultradian rhythms in time-series omics data. Fits cosinor regression models to estimate rhythm parameters (amplitude, phase, MESOR) and applies non-parametric tests (JTK_CYCLE, RAIN) to identify…
- ▌ Hi C Visualization Usage Guide · tools-only bundleThis skill covers visualizing Hi-C contact matrices, TADs, loops, and other genomic features using matplotlib, cooltools, and HiCExplorer.
- ▌ Population Structure Usage Guide · tools-only bundlePopulation structure analysis identifies genetic ancestry and stratification using PCA (continuous clustering) and ADMIXTURE (discrete ancestry proportions).
- ▌ Time Series De Usage Guide 2 · tools-only bundleIdentify genes with significant temporal expression patterns across time-course experiments using spline models, polynomial regression, or likelihood ratio tests.
- ▌ Co Expression Networks Usage Guide · tools-only bundleBuild weighted gene co-expression networks to identify modules of co-regulated genes and relate them to phenotypes.
- ▌ Structure Modification Usage Guide · tools-only bundleThis skill covers modifying protein structures: transforming coordinates, removing/adding atoms and residues, modifying B-factors and occupancies, and building structures programmatically.
- ▌ Splicing Pipeline Usage Guide · tools-only bundleComplete alternative splicing analysis workflow from raw RNA-seq FASTQ files to differential splicing results and visualizations. Includes QC checkpoints and best practices.
- ▌ Network Visualization Usage Guide · tools-only bundleThis skill enables AI agents to create static, interactive, and publication-quality visualizations of biological networks.
- ▌ Vcf Statistics Usage Guide · tools-only bundleThis guide covers generating variant statistics and quality metrics.
- ▌ Single Cell Preprocessing Usage Guide · tools-only bundleThis skill covers quality control, filtering, and normalization for single-cell RNA-seq data using both Seurat (R) and Scanpy (Python). These are essential steps before clustering and downstream analysis.
- ▌ Spectral Libraries Usage Guide · tools-only bundleBuild and use spectral libraries containing reference MS2 spectra for faster and more sensitive peptide identification in DIA and targeted proteomics.
- ▌ Nucleosome Positioning Usage Guide · tools-only bundleExtract nucleosome positions from ATAC-seq fragment size patterns using ATACseqQC or NucleoATAC to understand chromatin structure at promoters and regulatory regions.
- ▌ Co Expression Networks Usage Guide 2 · tools-only bundleBuild weighted gene co-expression networks to identify modules of co-regulated genes and relate them to phenotypes.
- ▌ Tumor Fraction Estimation Usage Guide · tools-only bundleEstimate circulating tumor DNA fraction from shallow whole-genome sequencing using ichorCNA. Detects copy number alterations and calculates ctDNA percentage for treatment monitoring.
- ▌ Wikipathways Enrichment Usage Guide · tools-only bundleWikiPathways is an open, collaborative platform for biological pathways with CC0 license, community curation, and support for 30+ species including many not covered by KEGG or Reactome.
- ▌ Alignment Validation Usage Guide · tools-only bundleValidate alignment quality with insert size distribution, proper pairing rates, GC bias, strand balance, and other post-alignment metrics before downstream analysis.
- ▌ Super Enhancers Usage Guide · tools-only bundleIdentify super-enhancers from H3K27ac ChIP-seq data using ROSE or HOMER. Super-enhancers are large clusters of enhancers that control cell identity genes and are often altered in cancer.
- ▌ Neoantigen Pipeline Usage Guide · tools-only bundleThis workflow identifies tumor-specific neoantigens from somatic mutations for personalized cancer vaccine design.
- ▌ Diversity Analysis Usage Guide 2 · tools-only bundleDiversity analysis characterizes microbial community structure through alpha (within-sample) and beta (between-sample) diversity metrics using phyloseq and vegan.
- ▌ De Visualization Usage Guide · tools-only bundleThis skill covers creating publication-quality visualizations for differential expression results, including MA plots, volcano plots, PCA plots, and heatmaps. Works with both DESeq2 and edgeR output.
- ▌ Clustering And Phenotyping Usage Guide · tools-only bundleUnsupervised clustering identifies cell populations without predefined gates. Useful for discovery and high-dimensional CyTOF/spectral flow data.
- ▌ Enrichment Visualization Usage Guide · tools-only bundleThe enrichplot package provides visualization functions for clusterProfiler results, including dot plots, bar plots, networks, and GSEA-specific plots.
- ▌ Differential Abundance Usage Guide · tools-only bundleDifferential abundance testing identifies taxa that differ significantly between experimental groups while accounting for the compositional nature of microbiome data.
- ▌ Species Delimitation Usage Guide · tools-only bundleDelimits putative species boundaries from molecular data using complementary approaches: distance-based partitioning (ASAP), tree-based branching rate models (bPTP, GMYC), and full coalescent analysis (BPP).