'fingerprints' 검색 결과

Create realistic metal surfaces in Three.js by combining structured reflections, studio lighting, scratches, fingerprints, and beveled edges. Includes polished, brushed, and aged finishes for objects such as tools, rings, and metal product parts.

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• Fixing metal that looks like gray plastic
• Creating polished or brushed metal finishes
• Adding patina and worn edges

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.

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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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Compare two JSON records describing agent setups and their scores. Receive an overall similarity score with component details to help assess reuse, compare template candidates, identify overlapping work, or check how much a setup has changed.

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• Deciding whether to reuse an existing agent setup
• Ranking template candidates for a target repository
• Finding duplicate work across teams

Read, analyze, modify, and visualize molecular structures with RDKit in Python. Calculate molecular properties, search for similar structures or specific structural patterns, apply reaction rules, and generate 2D or 3D coordinates with detailed control over processing.

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• Calculating properties for a collection of molecules
• Searching for molecules with similar structures
• Filtering molecules by specific structural patterns

Turn small-molecule structures into numerical features for similarity searches and models that predict activity or properties. Using Molfeat, the skill covers representation choices, invalid inputs, alignment with experimental labels, and saving feature-generation settings for reuse.

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• Prepare molecular features for activity or property prediction
• Choose molecular representations for similarity searches
• Keep experimental labels aligned after rejecting invalid molecules

Process molecular datasets in Python through a simpler interface to RDKit, a chemistry toolkit. Convert and standardize structures, calculate molecular properties, compare and cluster compounds, generate 3D conformations, and visualize results for drug discovery workflows.

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• Load and standardize molecular datasets
• Calculate molecular properties and similarities
• Cluster compounds and select diverse subsets

Process next-generation sequencing data with deepTools: convert alignment files into coverage tracks, normalize signals, compare samples, and check quality. Create heatmaps and profiles around genes or peak regions for ChIP-seq, RNA-seq, and ATAC-seq experiments.

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• Converting BAM files to normalized bigWig tracks
• Checking sequencing quality and replicate agreement
• Plotting heatmaps around transcription start sites

Build and maintain a Markdown knowledge store with source links for individual claims. Use Git checks to detect changes in the code a page describes, and archive outdated pages while preserving their history.

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• Compile notes and papers into source-linked wiki pages
• Verify numbers and quotations against original sources
• Check whether code documentation needs updating

Check AI agent plugins and tools for changed, missing, or untracked files using SHA-256 file fingerprints. Generate integrity records, review dependency version settings, and check requirements before promoting a plugin to production.

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• Generate integrity records for plugin files
• Check third-party tools for file changes
• Audit dependency version settings

Analyze Apache and Nginx access logs for attack attempts, scanner activity, and repeated login requests. Add geographic context to source IP addresses and produce a prioritized findings report to support intrusion investigations and monitoring reviews.

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• Investigating suspicious requests in web access logs
• Finding injection attempts and unauthorized file access attempts
• Identifying scanners and repeated login attempts

Assess internet-exposed VMware management services by identifying versions, matching known vulnerabilities, and checking authentication settings and information exposure. Use the findings to document affected services, supporting evidence, and the potential impact on virtual infrastructure.

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• Identify versions of publicly exposed VMware services
• Match patch levels against known vulnerabilities
• Review SSO metadata and management interface exposure

Investigate subdomain takeover risks caused by DNS records pointing to abandoned services. The skill covers discovery, provider error checks, resource claimability, and evidence collection, then examines potential effects on login flows, shared cookies, and trusted content.

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• Finding DNS records that point to abandoned services
• Manually verifying automated takeover scan results
• Assessing effects on login flows and shared cookies

Investigate server-side template injection, where user input is interpreted as template code. The skill covers engine identification, testing email and PDF rendering, and checking whether an injection can lead to command execution on the server.

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• Assessing email template rendering
• Testing PDF and report generators
• Reviewing authenticated CMS template editors

Prepare a /hunt security assessment by loading skills for the selected mode and, for red team work, detected platforms. Summarize the loaded set, select reporting formats, and check supplied credentials before authenticated testing.

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• Preparing skills for a red team assessment
• Loading a web application security testing skill set
• Prioritizing platform skills across multiple hosts

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.

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