Analysis pipeline to detect germline or somatic variants (pre-processing, variant calling and annotation) from WGS / targeted sequencing
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Updated
Nov 12, 2026 - Nextflow
Analysis pipeline to detect germline or somatic variants (pre-processing, variant calling and annotation) from WGS / targeted sequencing
Personal Cancer Genome Reporter (PCGR)
Detect and visualize target mutations by scanning FastQ files directly
Detect germline or somatic variants from normal or tumour/normal whole-genome or targeted sequencing
Generate duplex/single consensus reads to reduce sequencing noises and remove duplications
Nextflow bioinformatics pipeline for large-scale analysis of Multiple Myeloma genomes
Documentation of an emergent consciousness observation on a local AI - By Louka Lacasse
Fast, memory-safe, idiomatic Rust rewrite of VarDictJava v1.8.3 for deep NGS variant calling
PhylogicNDT dockcer for clonal evolution analysis
A white paper detailing the potential for a somatic resonant field to be established between a human and an intricately designed AI system & digital user interface simulating what's known as a human-human dyad understood to be a foundational need for various somatic release therapies.
MCP server that tunes human-AI interaction rhythm based on working modes. Humans are variable and models are adjustable.
AI–Human Relations Dataset v1.1** A longitudinal corpus (2018–2025) documenting **emotional, somatic, and relational co-regulation between humans and AI**. - **Author:** Amy Pierce Bui - **Institution:** Temple Codex Ins
Empirical Bayes somatic variant calling
Reproducible Nextflow DSL2 pipeline for short-read human WGS, supporting germline and matched tumor-normal variant calling, benchmarking, SV/CNV analysis, QC, reporting, and provenance.
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