biotender-max

Classifies germline variants using ACMG/AMP guidelines, generating clinical-grade reports with evidence audit trails.

Ranks gene-level CRISPR screen hits using guide-level count tables for enhanced functional genomics analysis.

Generates structured summaries of differential expression results, highlighting top genes and biological themes for publication-ready reports.

Transforms RNA-seq and scRNA outputs into rich visualizations and reports, enhancing data interpretation and presentation.

Identifies medications from photos and generates personalized dosage cards based on genotype data using Claude vision.

Generates phylogenetic distance matrices and trees from genomic VCF or FASTA data using the fastreeR toolkit.

Galaxy Bridge enables intelligent discovery and execution of bioinformatics tools through natural language, enhancing research workflows.

Compares genomes to George Church's data, estimating ancestry composition and IBS similarity for genetic analysis.

Fetches GWAS summary statistics for variants in a specified chromosomal region from the NHGRI-EBI GWAS Catalog.

Facilitates the import of Illumina DRAGEN result bundles into ClawBio for streamlined genomic analysis and reporting.

Synthesizes biomedical literature from PubMed and bioRxiv into structured reports and citation graphs, enhancing research efficiency.

Facilitates two-sample Mendelian Randomisation analysis from GWAS data, providing comprehensive estimators and sensitivity analysis.

Computes epigenetic age from DNA methylation arrays using PyAging clocks, ensuring reproducibility and detailed reporting.

Aggregates bioinformatics QC reports into a single MultiQC HTML report and markdown summary for streamlined analysis.

Facilitates downloading genomic, gene, virus, and taxonomy data from NCBI using command-line tools for bioinformatics research.

Generates personalized pharmacogenomic reports from DTC genetic data, providing insights on drug-gene interactions for better medication management.

Computes organ-specific biological age from Olink proteomic data using elastic net aging models for precise aging analysis.

Detects RNA-seq expression outliers for rare diseases, aiding diagnostics by scoring cases against a control reference panel.

Facilitates local single-cell latent embedding and batch-aware integration using scVI/scANVI from raw-count data.

Automates NGS read QC, alignment, and BAM processing using FastQC, BWA, and SAMtools for streamlined genomic workflows.