Genome Atlas Wgs · dayuguo bundle Audited, reproducible analysis of a personal whole-genome sequencing delivery (FASTQ / BAM / CRAM, GRCh37) into a bilingual (中文/English) single-file HTML report. Covers QC and a callable mask, Y and mtDNA haplogroups with heteroplasmy, 1000G ancestry PCA, local ancestry with a calibrated reference, ancient-DNA projection, ClinVar and ACMG screening, star-allele pharmacogenomics with copy number, HLA typing with disease and drug associations, polygenic scores, structural variants, repeat expansions, archaic introgression, blood groups, KIR, phasing and somatic signals. Use when a user hands you their own raw sequencing reads and asks to analyse, explore or report on their genome. Never for diagnosis or dosing.
