helixly

Re-audits a consumer DNA export's existing analysis documents into a deterministic, allow-list-cited, HelixyAI-branded HTML report. Use when the user wants to re-audit, rebuild, or verify a prior genome-analysis document set against their raw chip genotypes — e.g. "redo my genome report", "rebuild my health analysis from my 23andMe file", "verify what my prior genome docs claimed". It builds a genotype-truth INDEX from the raw export, audits the prior docs for unsupported or aspirational claims, rebuilds them with rsID + allow-list citations and a provenance block, and renders an interlinked HTML report. Requires a genome-reader install for parsing. Not a diagnostic tool — it restates authoritative-source guidance (CPIC/FDA/peer-reviewed) only and every recommendation ends with "consult your prescribing clinician".

Parses, summarizes, queries, and converts DNA and genome data files locally. Use whenever the user shares a FASTA, FASTQ, VCF, BAM/SAM/CRAM, BED, GFF/GTF, or a 23andMe / AncestryDNA / MyHeritage raw export — even if they don't name the format. Use for sequence inspection, variant counts, genotype lookups by rsID, region extraction, FASTQ QC, VCF Excel reports, format conversion, and DNA→protein translation. Do not use for de novo assembly, read alignment, variant calling, phylogenetic trees, or anything requiring an external paid API or uploading user data.