'transcript' 검색 결과

Analyze ad creatives (images and videos) extracted from competitor research. Use when given a directory of ad images, video files, or transcripts to evaluate ad quality, score visual and messaging effectiveness, assign a scale score for viral/engagement potential, and generate a cross-creative pattern summary. Triggered by requests like "analyze these ads", "score these creatives", "what hooks are competitors using", "evaluate the ad library", "give me a scale score", "analyze the ad folder", or "what's working in these ads".

한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.

Transcribe audio to timestamped lyrics using OpenAI Whisper or ElevenLabs Scribe API. Outputs LRC, SRT, or JSON with word-level timestamps. Use when users want to transcribe songs, generate LRC files, or extract lyrics with timestamps from audio.

한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.

Structured memory system for OpenClaw agents. Context death resilience (checkpoint/recover), structured storage, Obsidian-compatible markdown, local semantic search, and session transcript repair.

한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.

Transform learning content (like YouTube transcripts, articles, tutorials) into actionable implementation plans using the Ship-Learn-Next framework. Use when user wants to turn advice, lessons, or educational content into concrete action steps, reps, or a learning quest.

한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.

Analyze meeting transcripts to identify communication patterns, behavioral insights, and actionable feedback for improving communication and leadership effectiveness.

한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.

Calculates statistical power for high-dimensional genomics experiments (bulk RNA-seq, scRNA-seq, ATAC-seq, ChIP-seq, methylation, proteomics) under negative-binomial count models using RNASeqPower, PROPER, and simulation via powsimR, distinguishing per-gene from marginal (transcriptome-wide) power, the role of mean expression and dispersion, and the sequencing-depth-versus-replicate tradeoff. Covers simulation as the honest default for overdispersed counts, FDR-aware average power versus single-test power, observed/post-hoc power as an anti-pattern, and the winner's-curse / Type-S / Type-M consequences of underpowering. Use when planning replicate number for a sequencing experiment, deciding whether to add depth or samples, choosing closed-form versus simulation power, estimating power from pilot dispersions, or justifying replication in a grant. For clinical-trial power see clinical-biostatistics/power-and-sample-size; for the inverse sample-size question see experimental-design/sample-size.

한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.

Infer transcription factor regulons from single-cell RNA-seq with pySCENIC by combining GRNBoost2 co-expression, cisTarget motif-enrichment pruning, and AUCell per-cell activity scoring. Covers the motif-pruning-as-directionality principle, regulon specificity scoring, run-to-run stability, and database/species matching. Use when identifying TF regulons, scoring TF activity per cell, finding master regulators of cell identity, or comparing regulon activity across conditions. For enhancer-driven multiomic GRNs see multiomics-grn; for bulk inference and VIPER protein-activity see grn-inference.

한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.

Identifies differential m6A methylation between conditions from MeRIP-seq paired IP/input data using exomePeak2 (GC-bias-aware differential via its bam_ip/bam_input control + bam_treated_ip/bam_treated_input treatment arms), QNB beta-binomial, MeTDiff HMM, and RADAR, plus the paired-symmetric edgeR/DESeq2-on-peak-counts route when batch/lot covariates need fixed-effect handling that exomePeak2's API does not accept. Covers paired vs unpaired vs interaction designs, batch confounding and per-lot meta-analysis, the stoichiometry-vs-expression-vs-IP-efficiency confound, and effect-size filtering against under-powered N=2 designs. Use when comparing m6A across two or more conditions, choosing between exomePeak2/QNB/RADAR/MeTDiff for a design, handling batch confounding when exomePeak2's API is too rigid, distinguishing real hyper/hypo-methylation from expression shifts, applying effect-size thresholds, or planning orthogonal stoichiometry validation (GLORI/SAC-seq/m6Anet mod_ratio).

한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.

Imports gene expression count matrices from featureCounts, HTSeq, STAR ReadsPerGene, Salmon/kallisto via tximport or tximeta, RSEM, 10X Genomics MTX/H5, AnnData H5AD, and RDS. Handles silent-miscounting traps (featureCounts -p v2.0.2 API break, STAR strandedness column choice, salmon NumReads-sum without tximport, RSEM non-integer expected_count, GENCODE _PAR_Y suffix, zero-length-transcript TPM divide-by-zero), and encodes the tximport countsFromAbundance decision tree with the "lengthScaledTPM is not TPM" warning. Use when assembling a gene-by-sample count matrix from aligner or quantifier output, importing salmon/kallisto for DESeq2 vs limma-voom, choosing strandedness column for STAR, debugging zero-count panics, or building tx2gene mapping.

한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.

Infer gene regulatory networks from bulk or general expression data with mutual-information (ARACNe) and tree-ensemble (GENIE3, GRNBoost2) methods, and infer transcription-factor protein activity from regulons with VIPER and msVIPER. Covers the activity-not-edges paradigm, the undirected-association caveat, the DREAM5 wisdom-of-crowds and method-complementarity result, AUPRC-over-AUROC evaluation, and gold-standard incompleteness. Use when inferring a regulatory network from a bulk expression matrix, finding master regulators, or scoring TF activity from a signature. For single-cell motif-pruned regulons see scenic-regulons; for co-expression modules see coexpression-networks.

한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.

Detects m6A modifications from Oxford Nanopore direct-RNA-seq (DRS) signal using m6Anet (multiple-instance-learning over DRACH 5-mer signal). Covers the upstream pipeline (Dorado/Guppy basecalling -> minimap2 map-ont -> nanopolish eventalign -> m6anet dataprep -> m6anet inference), per-site vs per-read probability including the mod_ratio stoichiometry column, the DRACH-only constraint, minimum-coverage thresholds (20-50 reads/site), multi-condition comparison via xPore/Nanocompore/ELIGOS, Dorado native modification calling (RNA004, 2024+), and the cDNA-vs-DRS distinction (cDNA Nanopore CANNOT detect modifications). Use when calling m6A from ONT DRS without immunoprecipitation, choosing m6Anet vs xPore vs Nanocompore vs ELIGOS vs Dorado native, interpreting probability_modified vs mod_ratio vs per-read probabilities, deciding between m6Anet (known DRACH sites) and Dorado/Remora (genome-wide screening), pinning RNA002 vs RNA004 chemistry and basecaller versions, or troubleshooting eventalign/dataprep failures.

한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.

Performs differential expression on bulk RNA-seq count data with edgeR's negative-binomial GLM and quasi-likelihood F-test framework. Covers DGEList construction, filterByExpr, TMM/TMMwsp normalization, robust dispersion estimation, glmQLFit/glmQLFTest, TREAT for magnitude-bounded hypotheses, contrasts via no-intercept designs, voom and voomWithQualityWeights for heterogeneous samples, and the edgeR v4 bias-corrected APL changes. Use when running bulk DE with edgeR, choosing edgeR over DESeq2 (small n, transcript DE via catchSalmon, large samples), needing TREAT for a fold-change-threshold hypothesis, troubleshooting v3-to-v4 reproducibility, building paired or interaction designs, or handling library-quality heterogeneity.

한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.

Identifies super-enhancers from H3K27ac, MED1, or BRD4 ChIP-seq using ROSE, ROSE2, LILY, HOMER -style super, and ENCODE dELS cross-referencing. Handles peak stitching parameters, ranking choices, hockey-stick inflection, marker choice (H3K27ac vs MED1/BRD4), and cross-condition comparison with spike-in normalization. Constructs core regulatory circuitry (Saint-Andre 2016) from SE-encoded TFs. Use when identifying cell-identity / cancer-associated regulatory domains, comparing super-enhancers between conditions, identifying master transcription factor networks, or predicting BET-inhibitor responsiveness.

한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.

Detects allele-specific transcription factor or histone modification binding from heterozygous-variant ChIP-seq using WASP (reference-bias filter; mandatory upstream), RASQUAL (joint QTL + bias-corrected testing), BaalChIP (Bayesian beta-binomial with copy-number-aware overdispersion), and AlleleSeq (personalized diploid genome). Handles imprinted-locus awareness, X-inactivation artifacts, cancer copy-number imbalance, and integration with downstream caQTL / bQTL mapping. Use when identifying variants with allelic effects on TF binding, fine-mapping causal regulatory variants, validating deep-learning variant predictions, or characterizing cis-acting regulatory effects.

한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.

Performs gene-level association from GWAS summary statistics via genetically predicted tissue expression using FUSION, PrediXcan, S-PrediXcan, S-MultiXcan, UTMOST, MOSTWAS, kTWAS, EpiXcan, TIGAR-V2, and probabilistic fine-mapping with FOCUS and MA-FOCUS. Use when running TWAS from GWAS sumstats, prioritising candidate causal genes from a GWAS lead locus, picking single-tissue vs cross-tissue models, identifying LD-induced TWAS false positives, choosing ancestry-matched prediction weights, fine-mapping co-regulated TWAS hits, or triangulating TWAS with cis-eQTL Mendelian randomization and colocalization to nominate a causal gene.

한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.

Bulk-query Ensembl BioMart (and other BioMart instances) for cross-database ID mapping, gene/transcript/exon coordinates, and ortholog tables. Use when batch-converting Ensembl IDs to other namespaces (HGNC, RefSeq, UniProt, Entrez), pulling gene coordinate tables for thousands of genes, building ortholog wide-tables across species, or replacing slow Ensembl REST loops with one-shot bulk export. Encodes BioMart's XML query format, R biomaRt vs Python pybiomart trade-off, mart-vs-dataset hierarchy, and the URL endpoint that's BioMart-specific (separate from rest.ensembl.org).

한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.

Detect transcription factor binding footprints in ATAC-seq using TOBIAS, HINT-ATAC, Wellington, or scprinter. Use when identifying bound TF sites within accessible regions, correcting Tn5 insertion bias before footprinting, choosing between cleavage-based and aggregate-based footprinters, or comparing differential TF activity between conditions.

한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.

Process and generate multimedia content using Google Gemini API. Capabilities include analyze audio files (transcription with timestamps, summarization, speech understanding, music/sound analysis up to 9.5 hours), understand images (captioning, object detection, OCR, visual Q&A, segmentation), process videos (scene detection, Q&A, temporal analysis, YouTube URLs, up to 6 hours), extract from documents (PDF tables, forms, charts, diagrams, multi-page), generate images (text-to-image, editing, composition, refinement). Use when working with audio/video files, analyzing images or screenshots, processing PDF documents, extracting structured data from media, creating images from text prompts, or implementing multimodal AI features. Supports multiple models (Gemini 2.5/2.0) with context windows up to 2M tokens.

한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.

Process images, video, audio, PDFs with Gemini API. Generate images (Nano Banana 2), videos (Veo 3), speech (MiniMax TTS), music (MiniMax). Convert documents to Markdown. Multi-provider fallback (Gemini → MiniMax → OpenRouter). Activate when task references media files, asks to analyze/describe/transcribe/extract/generate/convert, or involves non-text binary files.

한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.

Read-only audit of `.claude/` structural overhead. Reports prioritized "remove X save Y tokens" recommendations against the model context window. NOT for monetary cost tracking — that's /mk:budget. NOT for transcript size monitoring — long-session continuity defers to Claude Code native compaction. NOT for runtime context decisions (what to read, when to compact) — see mk:context-engineering. Use when planning to add context capacity, diagnosing perceived slowdowns, or auditing health.

한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.

다중 세션 transcript에서 반복 실패 패턴(instinct)을 자동 채굴하여 신규 skill candidate 생성

한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.

Annotate speech/TTS datasets with per-clip quality metrics (MOS, SNR, STOI, pitch, bandwidth, speaking rate, WER/CER, gender/emotion), multi-ASR consensus transcription and speaker labeling using the audiogear pipeline; then filter clips by quality and build listenable HTML QA reports. Use when asked to compute audio dataset metrics, build extended_metadata.csv, transcribe unlabeled audio, select clean TTS training data, or QA a speech dataset.

한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.

YouTube transcripts to summaries, threads, blogs.

한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.

Azure OpenAI SDK for .NET. Client library for Azure OpenAI and OpenAI services. Use for chat completions, embeddings, image generation, audio transcription, and assistants.

한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.