「fingerprints」の検索結果

Core cheminformatics toolkit for SMILES/SDF/InChI parsing, descriptors (MW, LogP, TPSA), fingerprints, ECFP/Morgan fingerprints, substructure search, 2D/3D generation, similarity, reactions, and datamol-style molecule standardization when no separate wrapper skill is routed.

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Calculates molecular descriptors and fingerprints using RDKit. Computes Morgan fingerprints (ECFP), MACCS keys, Lipinski properties, QED drug-likeness, TPSA, and 3D conformer descriptors. Use when featurizing molecules for machine learning or filtering by drug-likeness criteria.

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。

Cheminformatics toolkit for molecular analysis and virtual screening: SMILES/SDF parsing, descriptors (MW, LogP, TPSA), fingerprints (Morgan/ECFP, MACCS), Tanimoto similarity, SMARTS substructure filtering, Lipinski drug-likeness, reaction enumeration, 2D/3D coordinates. For simpler API use datamol; use RDKit for fine-grained sanitization, custom fingerprints, or SMARTS/reaction control.

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Consolidate PostHog error tracking issues that are the same actual error reported under different fingerprints. Use when the user asks "why do I have so many TypeError issues that look the same?", "merge these duplicates", "stop splitting this error into new issues", or wants to clean up fingerprint sprawl. Decides between a one-shot merge of existing issues and a durable grouping rule that keeps future events from creating new fingerprints. Does NOT group conceptually similar bugs across different runtimes, SDKs, or call sites.

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Cheminformatics toolkit for fine-grained molecular control. SMILES/SDF parsing, descriptors (MW, LogP, TPSA), fingerprints, substructure search, 2D/3D generation, similarity, reactions. For standard workflows with simpler interface, use datamol (wrapper around RDKit). Use rdkit for advanced control, custom sanitization, specialized algorithms.

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ADR-152 — weighted similarity between two harness fingerprints (genome + score JSON). Returns overall score in [0,1] plus per-component breakdown (cosine over 9 numerics, categorical agreement over 4 enums, jaccard over agent_topology). Unblocks ADR-151 §3.2 Recommender, §3.3 Drift Detection, §3.5 Plugin Compat. Pure-TS, no `@metaharness/*` dep — preserves ADR-150's four architectural constraints.

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。

Cheminformatics toolkit for fine-grained molecular control. SMILES/SDF parsing, descriptors (MW, LogP, TPSA), fingerprints, substructure search, 2D/3D generation, similarity, reactions. For standard workflows with simpler interface, use datamol (wrapper around RDKit). Use rdkit for advanced control, custom sanitization, specialized algorithms.

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Featurizes small molecules with Molfeat for QSAR/QSPR, chemical similarity, virtual screening, and molecular ML. Covers ECFP/MACCS fingerprints, RDKit descriptors, pharmacophores, pretrained embeddings, configuration persistence, and molecule-to-label alignment.

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Pythonic wrapper around RDKit with simplified interface and sensible defaults. Preferred for standard drug discovery including SMILES parsing, standardization, descriptors, fingerprints, clustering, 3D conformers, parallel processing. Returns native rdkit.Chem.Mol objects. For advanced control or custom parameters, use rdkit directly.

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NGS analysis toolkit. BAM to bigWig conversion, QC (correlation, PCA, fingerprints), heatmaps/profiles (TSS, peaks), for ChIP-seq, RNA-seq, ATAC-seq visualization.

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Use when maintaining a durable Markdown knowledge store that agents compile from sources, when every number or quote in a wiki page must trace back to an immutable source, or when compiled pages need cheap drift detection against the code they describe. Teaches the raw/wiki/archive layout, per-claim provenance links, and git fingerprints for zero-token staleness checks.

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Parse Apache and Nginx access logs to detect SQL injection attempts, local file inclusion, directory traversal, web scanner fingerprints, and brute-force patterns. Uses regex-based pattern matching against OWASP attack signatures, GeoIP enrichment for source attribution, and statistical anomaly detection for request frequency and response size outliers.

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Build hyperrealistic PBR metal in Three.js: steel, brass, gold, copper and iron as true conductors (metalness 1, measured F0 tint, no albedo) with roughness-varied finishes (polished, brushed anisotropic, aged with patina and worn edges) lit by a dark HDR studio of real bright window cards prefiltered with PMREM. Use when metal looks like grey plastic, a dull blur, or a black hole; when blades, tools, rings, ingots, hardware or product metal need reflections with edges and structure; or when a finish needs scratches, streaks, fingerprints and bevels that catch light.

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VMware vSphere / vCenter Server external attack matrix — version fingerprinting, the high-impact CVE chain (CVE-2021-21972 vRealize unauth file upload, CVE-2021-21985 vSAN plugin RCE, CVE-2022-22954 Workspace ONE SSTI, CVE-2023-20887 Aria RCE, CVE-2024-37085 ESXi AD bypass, CVE-2023-34048 vCenter DCERPC OOB write APT-exploited), default credentials, SSO configuration disclosure, vmdir LDAP enumeration, ESXi Open SLP RCE history. ONLY for vCenter / Workspace ONE / Aria instances exposed to the internet — internal-network vCenter is out of scope per the external-only boundary. Use when recon shows port 443 with vCenter banner, `/ui` redirect, `/websso/SAML2/Metadata`, or VMware product fingerprints.

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Hunting skill for subdomain takeover vulnerabilities. Includes modern provider fingerprints — Microsoft Azure DevOps `cloudapp.azure.com` regional-pool re-issue (1-click OAuth ATO via wildcard `reply_to`, Binary Security), Zendesk help-desk takeover → email interception → password reset chain (0xprial writeup), Vercel `cname.vercel-dns.com` deleted-project takeover, plus general Fastly CDN service re-attach and S3 dangling-bucket cookie-scope techniques. Use when hunting subdomain takeover — emphasis on ATO-chain primitives (OAuth `redirect_uri`, cookie-domain, email DNS).

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Hunt server-side template injection (SSTI) across Jinja2 (Flask/Django), Twig (Symfony), Freemarker (Java), ERB (Rails), Spring, Velocity, Mako, Thymeleaf, Smarty. Detection probes use double-curly and dollar-curly math expressions evaluated server-side. Once an engine is fingerprinted, escalate to RCE via the engine-specific class-walker, callback-registrar, or Execute-utility patterns documented in disclosed reports. Detection patterns: error messages reveal engine, blank or numeric eval reveals expression mode. Targets: email templates, PDF/report generators, CMS preview features, error pages with user input. Use when hunting RCE via template rendering, when content shows engine fingerprints, when finding endpoints that compose strings with user input before render.

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Skill-set loader for /hunt orchestrator. Fingerprints the target, picks the right platform attack skills, and loads the Red Team or WAPT skill set. Use when /hunt has just received a mode answer (redteam or wapt + blackbox|greybox) and needs to load the appropriate skills and print the taxonomy. Not for direct user invocation.

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CVE lookup and applicability assessment domain card. Use after reconnaissance has identified products, versions, services, or fingerprints and red-team mode needs evidence-based CVE matching before deeper testing.

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Use when writing or debugging nvMolKit Python code for GPU-accelerated RDKit fingerprints, similarity, conformers, clustering, and molecular searches.

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Assemble a minimal redacted Attio diagnostic bundle with request fingerprints, schema context, retry evidence, and environment metadata. Use when escalating an Attio integration failure without leaking CRM data or secrets. Trigger with "Attio debug bundle", "Attio support evidence", or "collect Attio diagnostics".

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Cheminformatics toolkit for fine-grained molecular control. SMILES/SDF parsing, descriptors (MW, LogP, TPSA), fingerprints, substructure search, 2D/3D generation, similarity, reactions. For standard workflows with simpler interface, use datamol (wrapper around RDKit). Use rdkit for advanced control, custom sanitization, specialized algorithms.

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Performs molecular similarity searching using Tanimoto, Tversky, Dice, and cosine coefficients on bit/count fingerprints with explicit choice rules for symmetric vs asymmetric measures, scaffold-hopping vs lead-optimization regimes, activity-cliff diagnosis, and large-library nearest-neighbor methods (BulkTanimoto, MHFP6 LSH forest, USRCAT). Use when ranking compounds by structural resemblance to a query, clustering libraries, finding analogs, or diagnosing activity cliffs.

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Calculates molecular fingerprints (ECFP/Morgan, FCFP, MACCS, RDKit, AtomPair, TopologicalTorsion, Avalon, MAP4, MHFP6) and physicochemical descriptors (Lipinski, QED, TPSA, Crippen LogP, 3D shape) with explicit choice tables, bit vs count semantics, and partial-charge model selection. Use when featurizing molecules for similarity, QSAR, virtual screening, or ML, or selecting the correct fingerprint for a chemotype-aware task.

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 a final, machine-readable argument snapshot from current H3 sections and refresh section fingerprints before merge.

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。