「sequence analysis」の検索結果

Rigorous analysis expert covering limits, continuity, sequences, series, and measure theory foundations

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Produces structured U.S. legal audit summaries that distill compliance findings into executive-ready risk prioritization and remediation plans, covering likelihood/impact scoring, consequence analysis, and corrective actions with timelines and owners. Use for legal audits, compliance audits, regulatory audits, compliance gap analyses, risk assessments, audit report summaries, or remediation roadmaps. Trigger keywords: audit summary, compliance findings, audit report, risk prioritization, remediation plan, regulatory exposure, corrective action plan.

日本語の概要は準備中です。原文の説明を表示しています。

Discovers de novo motifs and tests known motif enrichment in ChIP-seq, ATAC-seq, or other peak sequences using HOMER, MEME-ChIP (STREME, CentriMo, TOMTOM, FIMO), monaLisa, and AME. Handles background selection (GC-matched, dinucleotide-shuffled, Markov order-2, peak-flanks), motif databases (JASPAR 2024 CORE PWMs, JASPAR 2026 deep-learning collection, HOCOMOCO v12, HOMER built-in), centrally-enriched motif testing, and differential motif analysis. Use when identifying TF binding motifs in peaks, testing for known TF enrichment, scanning for motif instances, comparing motif content between conditions, or interpreting motifs from deep learning models.

日本語の概要は準備中です。原文の説明を表示しています。

Analyze a single FASTA file (nucleotide or protein), compute sequence-level metrics (GC, ORFs, MW, pI, GRAVY, secondary-structure fractions) with Biopython, and write a Markdown report plus structured JSON for downstream chaining.

日本語の概要は準備中です。原文の説明を表示しています。

Knowledge base from the GAO Schedule Assessment Guide (GAO-16-89G, 2015). Use for building, assessing, or auditing a program's integrated master schedule (IMS): the ten best practices of a reliable schedule (capture, sequence, resource, duration, traceability, valid critical path, reasonable total float, schedule risk analysis, updating, baseline), the four characteristics (comprehensive, well-constructed, credible, controlled), critical path method arithmetic (forward/backward pass, total float), schedule risk analysis (Monte Carlo, contingency), statusing and baseline control, and the Appendix II audit triad. Scheduling/time-management oriented: it is the authority on schedule reliability, but it is NOT a cost-estimating guide, a full SE process model, an agile guide, or a risk-management framework — see sibling packs (gao-cost, dau-se-guidebook, nasa-schedule, nasa-risk) for those.

日本語の概要は準備中です。原文の説明を表示しています。

Use when the user asks to "build battle cards", "prep the sales team for launch", or "write the internal launch FAQ"; produces the internal enablement kit for a sales-led launch — battle cards vs each named alternative (where we win / where they win / trap questions, every fact traceable), a sales talk track derived from the PR-FAQ spine, an objection-handling table (objection → response → evidence), internal FAQ + CS macros, and an internal launch announcement with embargo discipline. Not for the external message house — use message-house-builder; not for competitor tracking itself — use competitor-tracker or competitor-analysis; not for outbound sequences — use cold-outbound-sequencer. 销售赋能/battle card/销售叙事/异议处理/内部FAQ

日本語の概要は準備中です。原文の説明を表示しています。

Use when working with Close Crm — close CRM management including leads, contacts, opportunities, activities, sequences, smart views, and custom fields. Covers pipeline velocity, calling metrics, email outreach performance, sequence engagement, and team productivity analysis.

日本語の概要は準備中です。原文の説明を表示しています。

Pixel-based motion and UI change analysis from frame sequences or screenshots using computer vision and visual comparison. Use when `.transition` or visual effects are not observable via MotionEyes logs, when you only have screenshots/video, when you need regression diffs across builds, or when you need to summarize on-screen changes without instrumentation. Do not use when MotionEyes traces are available and you need precise timing/values; use `motioneyes-animation-debug` instead.

日本語の概要は準備中です。原文の説明を表示しています。

Discovers de novo motifs and tests known motif enrichment in ChIP-seq, ATAC-seq, or other peak sequences using HOMER, MEME-ChIP (STREME, CentriMo, TOMTOM, FIMO), monaLisa, and AME. Handles background selection (GC-matched, dinucleotide-shuffled, Markov order-2, peak-flanks), motif databases (JASPAR 2024 CORE PWMs, JASPAR 2026 deep-learning collection, HOCOMOCO v12, HOMER built-in), centrally-enriched motif testing, and differential motif analysis. Use when identifying TF binding motifs in peaks, testing for known TF enrichment, scanning for motif instances, comparing motif content between conditions, or interpreting motifs from deep learning models.

日本語の概要は準備中です。原文の説明を表示しています。

Identify section boundaries and content sequences within a scraped webpage for AEM Edge Delivery Services import. Performs two-level analysis (sections, then sequences per section) and surveys available blocks.

日本語の概要は準備中です。原文の説明を表示しています。

Discovers de novo motifs and tests known motif enrichment in ChIP-seq, ATAC-seq, or other peak sequences using HOMER, MEME-ChIP (STREME, CentriMo, TOMTOM, FIMO), monaLisa, and AME. Handles background selection (GC-matched, dinucleotide-shuffled, Markov order-2, peak-flanks), motif databases (JASPAR 2024 CORE PWMs, JASPAR 2026 deep-learning collection, HOCOMOCO v12, HOMER built-in), centrally-enriched motif testing, and differential motif analysis. Use when identifying TF binding motifs in peaks, testing for known TF enrichment, scanning for motif instances, comparing motif content between conditions, or interpreting motifs from deep learning models.

日本語の概要は準備中です。原文の説明を表示しています。

Identify section boundaries and content sequences within a scraped webpage for AEM Edge Delivery Services import. Performs two-level analysis (sections, then sequences per section) and surveys available blocks.

日本語の概要は準備中です。原文の説明を表示しています。

Queries 20+ bioinformatics resources through CLI/Python. Supports quick lookups of gene info, BLAST/BLAT, viral sequence downloads, PDB/mmCIF structures, G2P residue annotations, enrichment analysis, OpenTargets, COSMIC, CELLxGENE, and 8cube mouse specificity/expression data. Best for interactive exploration and simple queries. For batch processing or advanced BLAST use biopython; for multi-database Python workflows use bioservices.

日本語の概要は準備中です。原文の説明を表示しています。

Internal downstream skill for ctf-sandbox-orchestrator. CTF-sandbox workflow for packet capture analysis, session reconstruction, application-protocol decoding, stream reassembly, beacon timing, and packet-to-process correlation. Use when the user asks to analyze a PCAP, rebuild TCP or UDP sessions, decode HTTP, WebSocket, DNS, custom C2, or binary protocols, extract transferred artifacts, or tie packet sequences to host or malware behavior. Use only after `$ctf-sandbox-orchestrator` has already established sandbox assumptions and routed here.

日本語の概要は準備中です。原文の説明を表示しています。

Detect anomalies in Modbus/TCP and Modbus RTU industrial traffic via function code monitoring, register range validation, timing analysis, and deep packet inspection, using Zeek's Modbus analyzer, Suricata IDS with OT rules, and Python Markov chain models of normal transaction sequences. Use for deploying Modbus IDS in OT environments, baselining polling patterns, investigating suspicious Modbus traffic, or building function code allowlists.

日本語の概要は準備中です。原文の説明を表示しています。

Generate forensic super-timelines with Plaso's log2timeline.py, pinfo.py, psort.py, and psteal.py CLI tools (fusing file-system MACB, registry, EVTX, browser history, prefetch, LNK, and more), then triage and filter the results in Timesketch. Use when reconstructing the full sequence of events on a compromised or forensically imaged host during a DFIR investigation.

日本語の概要は準備中です。原文の説明を表示しています。

Build collaborative forensic incident timelines using Timesketch to ingest, normalize, and analyze multi-source event data (including Plaso output) for attack chain reconstruction and investigation documentation. Use when reconstructing the sequence of events during an incident investigation or when multiple analysts need to jointly tag, annotate, and search a shared DFIR timeline.

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Retrieve and analyze AlphaFold predicted structures for a protein. Use when the user provides a specific UniProt Accession ID and wants structural confidence metrics (pLDDT), domain boundary analysis, or disorder assessment. Do not use if the user only has a protein name, gene name, or amino acid sequence — ask for a UniProt ID first.

日本語の概要は準備中です。原文の説明を表示しています。

Visualize, analyze, and render protein and molecular structures using PyMOL. Use when the user wants to create images of protein structures, perform structural alignments or superposition, measure distances or contacts, highlight binding sites or active site residues, color by B-factor/pLDDT, or analyze protein-ligand interactions. Do not use for docking, molecular dynamics, or sequence-only analysis.

日本語の概要は準備中です。原文の説明を表示しています。

Amplicon sequence variant (ASV) inference from 16S rRNA or ITS amplicon sequencing using DADA2. Covers quality filtering, error learning, denoising, and chimera removal. Use when processing demultiplexed amplicon FASTQ files to generate an ASV table for downstream analysis.

日本語の概要は準備中です。原文の説明を表示しています。

Read, 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.

日本語の概要は準備中です。原文の説明を表示しています。

Gets people to actually use what was delivered — stakeholder analysis, communication, training, resistance, and measuring adoption. Use this to plan a rollout, recover an implementation nobody is using, handle resistance to a change, sequence communications, or work out why a technically successful project changed nothing.

日本語の概要は準備中です。原文の説明を表示しています。

A high-performance Rust toolkit (with Python bindings and a CLI) for genomic interval analysis; use it when you need fast overlap queries, coverage track generation, genomic tokenization for ML, reference sequence verification, or fragment processing.

日本語の概要は準備中です。原文の説明を表示しています。

Systematically maps mechanism evidence for a disease from molecules to pathways, cell types, tissues, biological consequences, and clinical phenotypes. Always use this skill when a user needs a layered mechanism evidence chain rather than a flat summary or immediate gap analysis. Formal literature citations must be real and verifiable.

日本語の概要は準備中です。原文の説明を表示しています。