T2T-CHM13 improves read mapping and detection of clinically relevant genetic variation in the Swedish population. #HumanGenome #ReferenceGenome #T2t_CHM13 #SwedishPopulation #GeneticVariation @genomeresearch.bsky.social 🧬 🖥️
genome.cshlp.org/content/earl...

Complete reference genome and pangenome improve genome-wide detection and interpretation of DNA methylation using sequencing and array data. #T2T_CHM13 #Pangenome #Epigenetics #MethylationArrays @cp-cellreports.bsky.social‬
www.cell.com/cell-reports...