Analyzes base editing and prime editing outcomes including editing efficiency, bystander edits, and indel frequencies.
Develop a Base44 app remotely from your own coding agent (Claude Code, claude.ai, or any MCP client) by connecting it to the Base44 sandbox.
Extracts clinical trial baseline data (study, region, participants, etc.) from article text or PMID. Checks PubMed for metadata; always falls back to LLM extraction for full…
Use when performing 3+ similar operations like file edits, searches, or git operations. Triggers on repetitive tasks, "do the same for", loop-like patterns.
Replace human review with reproducible evidence. Always provide deterministic receipts, never narratives.
Guides development and approval of Binding Corporate Rules under GDPR Article 47 for intra-group international data transfers. Covers Art.
Create and manage blog posts on Bear Blog (bearblog.dev). Supports extended Markdown, custom attributes, and browser-based publishing.
把用户提供的素材（网页 URL / PDF / DOCX / Markdown / 纯文本 / 截图 / 粘贴材料）编辑、设计成一篇美丽的、可离线打开和分享的**单文件 HTML 网页文章**。基于 reacticle 组件协议：不手写裸 HTML/CSS，而用语义组件 + 受主题约束的 Raw 自由层；按…
A source-backed ASE skill for Beekeeper Studio, the SQL editor and database manager for Linux, macOS, and Windows.
Manage and tag music libraries with beets, the Python-based CLI tool that auto-tags audio files using MusicBrainz metadata.
Spezialisierter Agent für Kampf-, Sozial- und Erkundungsbegegnungen. Balanciert Herausforderungen nach Erfahrungsstufe und sorgt für taktische Tiefe und narrative Spannung — für…
Provides Framer Motion animation patterns and best practices specific to the Bellog blog project. Triggers when implementing animated components or interactions.
Provides theme integration guidelines and CSS variable usage patterns for the Bellog blog. Triggers when creating styled components or working with colors.
Migrates content from Markdown, Jekyll, Hugo, or other SSGs to Bengal. Use when converting a site, importing posts, or restructuring content.
Scaffolds a new Bengal static site with config, content structure, and theme. Use when creating a new site, starting a blog, or converting a project to Bengal.
Transform text into Ben Church's authentic blog writing voice. Use when the user asks to "benify", "write like Ben", "rewrite in Ben's voice", "make this sound like me", "apply my…
Prüft Videoüberwachung, Zutrittslogs, Fernwartung, Auftragsverarbeitung und Drittlandzugriffe im Energierecht.
The best-youtube-video-editor skill on ClawHub transforms how YouTube creators produce content by enabling conversational, AI-driven video editing without timelines or complex…
Influencer-Recht: Betriebsfeier und Content – KUG, DSGVO, Mitarbeiterfotos, Veröffentlichungspflichten und Datenschutz im Influencer-Recht.
Beverage commercial photography expert. Given a product image, automatically analyzes product → selects aesthetic style → builds Prompts → batch generates 5 × 4K images (dynamic…
Professional web design skill for AI coding agents. Overrides LLM default UI biases. Non-generic, minimalist, animated frontends. Framework-agnostic.
Spezialfall Mediendienste: Untertitel, Audiodeskription, Gebaerdensprache, ARD/ZDF-Linie, AVMD-Richtlinie, MStV. Pflichten fuer Streaming-Anbieter und Mediatheken.
BibiGPT CLI for summarizing videos, audio, and podcasts directly in the terminal. Use when the user wants to summarize a URL (YouTube, Bilibili, podcast, etc...
Analyze a BibTeX bibliography and generate a thematic tree diagram in Mermaid, plus a suggested article title (TARGET_TITLE). Stage 1 of the academic-pipeline.
Use when after bias correction of ATAC-seq reads (via ATACorrect) when you have a bias-corrected bigWig file and need to measure transcription factor footprint strength within…
A comprehensive Bilibili toolkit that integrates hot trending monitoring, video downloading, video watching/playback, subtitle downloading, and video publishing capabilities into…
Extract subtitles and transcripts from Bilibili and YouTube videos. Use when the user wants to get subtitles from B站 (Bilibili) or YouTube, extract Chinese/Japanese video…
Use when paired tr.md and en.md files need a parity verdict, when titles, frontmatter, headings, or DOI sets may have drifted between languages, or when a bilingual document is…
Drafting deutsch-englischer Vertraege in Side-by-Side- oder Stacked-Layout. Bestimmt den Anwendungsfall (true bilingual, sovereign language, courtesy translation), waehlt das…
Corporate Billing Narratives: Erstellt deal-taugliche Time Narratives, Phasenbudgets, Workstream-Rechnungen, Cap/Success-Fee-Hinweise und Matter-Controlling.
Russian language calibration for Billy Milligan agents. Load when session language is RU. Contains native speech patterns, swearing vocabulary, pet name styles, and anchor…
Annotate CLIP-seq binding sites to genomic features including 3'UTR, 5'UTR, CDS, introns, and ncRNAs. Use when characterizing where an RBP binds in transcripts.
Detect transcription factor binding sites through footprinting analysis in ATAC-seq data using TOBIAS.
Detect transcription factor binding footprints in ATAC-seq using TOBIAS, HINT-ATAC, Wellington, or scprinter.
Analyze transcription factor motif accessibility variability using chromVAR. Use when identifying which TF motifs show variable accessibility across samples or conditions in…
Bulk-query Ensembl BioMart (and other BioMart instances) for cross-database ID mapping, gene/transcript/exon coordinates, and ortholog tables.
Performs gene-level association from GWAS summary statistics via genetically predicted tissue expression using FUSION, PrediXcan, S-PrediXcan, S-MultiXcan, UTMOST, MOSTWAS, kTWAS,…
De novo motif discovery and known motif enrichment analysis using HOMER and MEME-ChIP. Identify transcription factor binding motifs in ChIP-seq, ATAC-seq, or other genomi — from…
Detects allele-specific transcription factor or histone modification binding from heterozygous-variant ChIP-seq using WASP (reference-bias filter; mandatory upstream), RASQUAL…
De novo motif discovery and known motif enrichment analysis using HOMER and MEME-ChIP. Identify transcription factor binding motifs in ChIP-seq, ATAC-seq, or other genomi — from…
ChIP-seq peak calling using MACS3 (or MACS2). Call narrow peaks for transcription factors or broad peaks for histone modifications.
Identifies super-enhancers from H3K27ac ChIP-seq data using ROSE and related tools. Use when studying cell identity genes, cancer-associated regulatory elements, or master…
Identifies super-enhancers from H3K27ac, MED1, or BRD4 ChIP-seq using ROSE, ROSE2, LILY, HOMER -style super, and ENCODE dELS cross-referencing.
Queries PharmGKB / CPIC / DPWG for drug-gene interactions; calls CYP2D6/CYP2C9/CYP2C19/DPYD/TPMT/NUDT15/UGT1A1/SLCO1B1 star alleles and phenotype with PharmCAT, Cyrius (CYP2D6…
Annotate CLIP-seq peaks or crosslink sites to RNA features (5'UTR, CDS, 3'UTR, intron, splice junction, snoRNA, tRNA, ncRNA, repeat elements) with ChIPseeker, RCAS, RBP-Maps (Yeo…
Infer integer allele-specific copy number, tumor purity, and ploidy from tumor sequencing by jointly modeling read depth (logR) and B-allele frequency (BAF) with ASCAT, Sequenza,…
Annotate CNVs with genes, pathways, and clinical significance. Use when interpreting CNV calls or identifying affected genes from copy number analysis.
Annotate copy number variant segments with overlapping genes, dosage-sensitivity scores, cancer driver databases, population frequencies, and clinical-variant content.
Visualize copy number profiles, segments, and compare across samples. Create publication-quality plots of CNV data from CNVkit, GATK, or other callers.
Visualize copy number profiles, segments, allele-specific tracks, and cohort patterns from CNVkit, GATK, ASCAT, FACETS, Sequenza, and other callers.
Detect copy number variants from targeted/exome sequencing using CNVkit. Supports tumor-normal pairs, tumor-only, and germline CNV calling.
Detect somatic and germline copy number variants from targeted, exome, and whole-genome sequencing with CNVkit, a read-depth caller that combines on-target and off-target…
Normalize read-depth copy-ratio profiles and segment them into copy-number regions using circular binary segmentation (CBS, DNAcopy), hidden Markov models, HaarSeg, and…
Resolve the architecture of focal oncogene amplifications — extrachromosomal DNA (ecDNA), breakage-fusion-bridge (BFB) cycles, homogeneously staining regions (HSR), and linear…
Call copy number variants using GATK best practices workflow. Supports both somatic (tumor-normal) and germline CNV detection from WGS or WES data.
Call copy number variants with the GATK best-practices workflows — the somatic CNV pipeline (CollectReadCounts, DenoiseReadCounts with tangent normalization, ModelSegments,…
Classify constitutional (germline) copy number variants for clinical reporting using the 2019 ACMG/ClinGen technical standards points-based framework, with ClassifyCNV an — from…
Quantify homologous recombination deficiency (HRD) from tumor copy number using the three genomic-scar metrics — loss of heterozygosity (LOH), large-scale state transitions (LST),…
Identify recurrent and driver copy number alterations across a tumor cohort with GISTIC2 (G-score, Ziggurat deconstruction, focal vs broad/arm-level analysis, q-values from…
Resolve subclonal copy number, whole-genome doubling, and copy-number tumor evolution from bulk sequencing with Battenberg, TITAN, and MEDICC2.