Documentation

Docs, README files, API references, tutorials, specs, and changelogs

skills in category: 14,027
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Showing 601–624 of 14,027 skills

BookAManage book projects - create/edit parts, chapters, sections. Use when user wants to add, rename, delete, or reorganize book structure elements. Triggers on "new chapter", "add section", "rename part", "delete appendix", "move chapter".documentationpythonbashVotes: 0GitHub stars: 2
Book ReaderARead and search digital books (PDF, EPUB, MOBI, TXT). Use when answering questions about a book, finding quotes or passages, navigating to specific pages or chapters, or extracting information from documents.documentationgobashVotes: 0GitHub stars: 2
Book PublisherAProfessional book publishing from Markdown, Word, or text to PDF/EPUB. Use when creating books, converting manuscripts to PDF, generating covers (Kindle and paperback with spine), building indexes with real page numbers, creating table of contents, or formatting chapters. Handles trade paperback (5.5x8.5), two-pass TOC generation, EPUB conversion, and Amazon KDP requirements.documentationpythongoVotes: 0GitHub stars: 2
Bonfire ContextALoad .bonfire/index.md context to understand ongoing work, previous decisions, blockers, and session history. Use when user references past work or asks about project status.documentationgogitVotes: 0GitHub stars: 2
BloginterviewerAInterview to capture author identity, voice, and brand language for the blog. Use when Ian mentions "interview me", "my background", "author profile", "writing style", "brand voice", "who am I", or wants to define narrative preferences and tone.documentationgoexpressVotes: 0GitHub stars: 2
Blog WriterACreate category-aware, AEO-optimized blog posts for Lightfast. Use when writing technology deep-dives, company announcements, or product launches.documentationgoVotes: 0GitHub stars: 2
Blog Writer 2ATransform brain dumps into polished technical blog posts. Use when you have scattered ideas, talking points, or code examples that need organizing into a cohesive developer-focused post.documentationVotes: 0GitHub stars: 2
Blockbench Mcp OverviewAOverview of the Blockbench MCP server tools, resources, and prompts. Use to understand the full MCP capability set, learn how tools work together, or when starting a new Blockbench project. Covers all domains (modeling, animation, texturing, PBR, UI, camera) and their MCP interfaces.documentationgonodeVotes: 0GitHub stars: 2
BitsATrack and manage work items, tasks, issues, and todos with dependencies using bits. Use when user needs to create tasks, track progress, manage blockers, find ready work, claim/release tasks, close completed work, or organize multi-step projects. Triggers on "bits", "task", "issue", "backlog", "blockers", "dependencies", "what's ready", "track this", "add to my list", "what should I work on".documentationbashgitVotes: 0GitHub stars: 2
Bio Variant Calling Structural Variant CallingACall 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.documentationgobashVotes: 0GitHub stars: 2
Bio Variant Calling Clinical InterpretationAClinical variant interpretation using ClinVar, ACMG guidelines, and pathogenicity predictors. Prioritize variants for diagnostic and research applications. Use when interpreting clinical significance of variants.documentationpythongoVotes: 0GitHub stars: 2
Bio Single Cell PreprocessingAQuality control, filtering, and normalization for single-cell RNA-seq using Seurat (R) and Scanpy (Python). Use for calculating QC metrics, filtering cells and genes, normalizing counts, identifying highly variable genes, and scaling data. Use when filtering, normalizing, and selecting features in single-cell data.documentationpythonVotes: 0GitHub stars: 2
Bio Single Cell Markers AnnotationAFind marker genes and annotate cell types in single-cell RNA-seq using Seurat (R) and Scanpy (Python). Use for differential expression between clusters, identifying cluster-specific markers, scoring gene sets, and assigning cell type labels. Use when finding marker genes and annotating clusters.documentationpythonexpressVotes: 0GitHub stars: 2
Bio Single Cell ClusteringADimensionality reduction and clustering for single-cell RNA-seq using Seurat (R) and Scanpy (Python). Use for running PCA, computing neighbors, clustering with Leiden/Louvain algorithms, generating UMAP/tSNE embeddings, and visualizing clusters. Use when performing dimensionality reduction and clustering on single-cell data.documentationpythongoVotes: 0GitHub stars: 2
Bio Metabolomics Msdial PreprocessingAMS-DIAL-based metabolomics preprocessing as alternative to XCMS. Covers peak detection, alignment, annotation, and export for downstream analysis. Use when processing MS-DIAL output files for R/Python analysis or when preferring GUI-based preprocessing.documentationpythongoVotes: 0GitHub stars: 2
Bio Metabolomics Metabolite AnnotationAMetabolite identification from m/z and retention time. Covers database matching, MS/MS spectral matching, and confidence level assignment. Use when assigning compound identities to detected features in untargeted metabolomics.documentationpythonbashVotes: 0GitHub stars: 2
Bio Local BlastARun local BLAST searches using BLAST+ command-line tools. Use when running fast unlimited searches, building custom databases, performing large-scale analysis, or when NCBI servers are slow or unavailable.documentationpythongoVotes: 0GitHub stars: 2
Bio Genome Intervals Proximity OperationsAFind nearest features, search within windows, and extend intervals using closest, window, flank, and slop operations. Use when performing TSS proximity analysis, assigning enhancers to genes, defining promoter regions, or finding nearby genomic features.documentationpythongoVotes: 0GitHub stars: 2
Bio Genome Intervals Bed File BasicsABED file format fundamentals, creation, validation, and basic operations. Covers BED3 through BED12 formats, coordinate systems, sorting, and format conversion using bedtools and pybedtools. Use when working with genomic coordinates or preparing interval files for downstream tools.documentationpythonbashVotes: 0GitHub stars: 2
Bio Flow Cytometry Clustering PhenotypingAUnsupervised clustering and cell type identification for flow/mass cytometry. Covers FlowSOM, Phenograph, and CATALYST workflows. Use when discovering cell populations in high-dimensional cytometry data without predefined gates.documentationexpressVotes: 0GitHub stars: 2
Bio Clinical Databases Dbsnp QueriesAQuery dbSNP for rsID lookups, variant annotations, and cross-references to other databases. Use when mapping between rsIDs and genomic coordinates or retrieving basic variant information.documentationpythongoVotes: 0GitHub stars: 2
Bio Alignment IoARead, write, and convert multiple sequence alignment files using Biopython Bio.AlignIO. Supports Clustal, PHYLIP, Stockholm, FASTA, Nexus, and other alignment formats for phylogenetics and conservation analysis. Use when reading, writing, or converting alignment file formats.documentationpythonVotes: 0GitHub stars: 2
BillingADebug, edit, and fix billing endpoints. Covers legacy endpoints (attach/checkout/cancel) and the new v2 4-layer architecture (setup, compute, evaluate, execute). Use when working on billing, subscription, invoicing, or Stripe integration code.documentationtypescriptdebuggingVotes: 0GitHub stars: 2
Benchmark OnboarderAOnboard AI creativity benchmarks into HELM-compliant Scenario implementations. Use when asked to onboard a benchmark, create a HELM scenario, process a paper into evaluation code, convert a dataset to HELM format, or when the user mentions "creativity benchmark", "task.py", or "scenario.py".documentationpythonrustVotes: 0GitHub stars: 2