Everything in the catalog

Contract review assistant analyzing agreements against playbooks.

Prepare structured briefings for meetings with legal relevance and track action items.

Adversarial verification for AI-generated legal content.

Dispute analysis and mediation preparation framework.

Deep clause-by-clause NDA review from Recipient or Discloser perspective.

Rapid NDA screening with GREEN/YELLOW/RED classification.

Statute and regulation interpretation framework.

Negotiation frameworks for technology services agreements, B2B contracts, and professional services deals.

Assess IT vendors and third-party partners with multi-factor risk scoring and regulatory compliance checklists.

Audit whistleblower systems and draft compliant reporting policies.

Unified analysis pipeline for affinity-based proteomics platforms — Olink (PEA, NPX) and SomaLogic SomaScan (SOMAmer, RFU).

Given an article DOI or PubMed ID, discover and download the genomics data files deposited by the authors (VCF, FASTA, H5AD, CSV, JSON, BAM, etc.) from public…

Search scientific papers via the BGPT MCP server and retrieve structured experimental data — methods, results, conclusions, quality scores, and 25+ metadata…

Run read-only SQL against BigQuery public datasets with local result capture, cost safeguards, and reproducibility outputs.

Bioconductor package discovery, workflow recommendation, setup inspection, and starter code generation grounded in official Bioconductor containers and…

Cell segmentation in fluorescence microscopy images.

Given a gene and a single-cell atlas, compute how cell-type-specific its expression is — the tau specificity index, Sarle's expression bimodality coefficient…

Methylation cycle analysis — enzymatic activity profiles, Net Methylation Capacity, BH4 axis estimates, compound heterozygosity detection from SNP genotype…

Classify germline variants from VCF/BCF files according to the ACMG/AMP 2015 28-criteria evidence framework and generate clinical-grade interpretation reports…

Classify structural variants / copy-number variants (deletions and duplications) using the ClinGen / ACMG 2019 (Riggs et al.

Population genetics of pre-aligned DNA sequences or multi-sample VCFs using selected DnaSP 6 methods.

Objective-driven pooled viability screen analysis: QC, hit calling, context-selectivity, biomarker sweep, and ranked repurposing candidates.

Compute HEIM diversity and equity metrics from VCF or ancestry data.

Statistical fine-mapping of GWAS loci using SuSiE, SuSiE-inf, and Approximate Bayes Factors to identify credible sets and posterior inclusion probabilities…