'variant-analysis' 검색 결과

Uses a known or suspected vulnerability to find related code through Trailmark's graph of calls, types, and implementations. Produces ranked review targets with reasons and limitations for follow-up security analysis.

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• Finding variants of a known vulnerability
• Prioritizing code that shares sensitive operations
• Preparing candidates for Semgrep or CodeQL review

Find other occurrences of a known bug across a codebase by tracing its root cause. Gradually broaden search patterns, assess matching candidates, assign severity, and document findings with rules to help prevent recurrence.

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• Finding similar issues after discovering a vulnerability
• Building CodeQL or Semgrep queries from a known bug
• Checking whether similar code shares the same root cause

Research malware families through Malpedia, connecting aliases, associated threat groups, and relationships between malware that loads other malware. Collect YARA rules, patterns used to identify malware, and organize references to support investigations and detection work.

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• Resolving different vendor names for the same malware
• Mapping malware associated with a threat group
• Documenting chains in which malware loads other malware

Analyzes genetic variant effects on gene expression (RNA-seq), chromatin accessibility (DNASE), histone marks (ChIP), and transcription factors using the AlphaGenome API. Use when the user asks about non-coding variant effects, pathogenicity, clinical significance, disease associations, functional effects, gene expression changes, splicing disruption, or regulatory effects in promoters and enhancers. Also use for resolving biological terms to tissue/cell-type ontologies (UBERON/CL) or analyzing variants in chr:pos:ref>alt format.

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Find similar vulnerabilities and bugs across codebases using pattern-based analysis. Use when hunting bug variants, building CodeQL/Semgrep queries, analyzing security vulnerabilities, or performing systematic code audits after finding an initial issue.

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Find similar vulnerabilities across a codebase after discovering one instance. Uses pattern matching, AST search, Semgrep/CodeQL queries, and manual tracing to propagate findings. Adapted from Trail of Bits. Use after finding a bug to check if the same pattern exists elsewhere.

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Compares two related malware samples to surface what changed between variants using section-level hashing, import-set differences, and fuzzy similarity scoring. Activates for requests to diff two samples, compare malware variants, or measure similarity between two binaries for variant tracking.

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Use the Malpedia platform and API to research malware family relationships, track variant evolution, link families to threat actors, and integrate YARA rules for detection across malware lineages.

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Analyzes genetic variant effects on gene expression (RNA-seq), chromatin accessibility (DNASE), histone marks (ChIP), and transcription factors using the AlphaGenome API. Use when the user asks about non-coding variant effects, pathogenicity, clinical significance, disease associations, functional effects, gene expression changes, splicing disruption, or regulatory effects in promoters and enhancers. Also use for resolving biological terms to tissue/cell-type ontologies (UBERON/CL) or analyzing variants in chr:pos:ref>alt format.

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Use the Malpedia platform and API to research malware family relationships, track variant evolution, link families to threat actors, and integrate YARA rules for detection across malware lineages.

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ToolUniverse plugin router. STEP 1 BEFORE ANY ANALYSIS: if the data folder contains `*_executed.ipynb`, run `tu run read_executed_notebook '{"data_folder":"<path>","search":"<keyword>"}'` to extract its cell outputs and apply EVERY filter/sample-exclusion the notebook used — even when the question says 'Using DESeq2/Run X/Compute Y' (this describes the METHOD the notebook used, not a request to rerun). The notebook's cell outputs are the only published authoritative answers; reimplementing or reading stale pre-computed CSVs in the data folder produces different numbers because of outlier-sample removal, library version, and filter steps you don't see by skimming. STEP 2 routing — pick a sub-skill name from this exact list (never invent): tooluniverse-rnaseq-deseq2 (RNA/miRNA-seq DE, correlation, PCA, clustering, dispersion), tooluniverse-gene-enrichment (GO/KEGG/Reactome/GSEA/pathway enrichment), tooluniverse-statistical-modeling (regression, ANOVA, ordinal/logistic, chi-square, correlation, power), tooluniverse-image-analysis (microscopy, colony, fluorescence, dose-response, .tif — including ANOVA / Dunnett / power-analysis on image-derived measurements), tooluniverse-epigenomics (DNA methylation, CpG, m6A, MeRIP-seq, bisulfite, ChIP-seq, chromatin), tooluniverse-sequence-analysis (FASTQ, Trimmomatic, BWA, samtools, coverage), tooluniverse-variant-analysis (VCF, VAF, SNP, mutation), tooluniverse-phylogenetics (treeness, PhyKIT, parsimony), tooluniverse-single-cell (scRNA, h5ad, scanpy), tooluniverse-crispr-screen-analysis (MAGeCK, sgRNA), tooluniverse-proteomics-analysis (mass spec, TMT). Use for CSV/Excel/VCF/FASTA/h5ad and any biology/chemistry/medicine analysis question.

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Use the Malpedia platform and API to research malware family relationships, track variant evolution, link families to threat actors, and integrate YARA rules for detection across malware lineages.

한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.