Analysis of chromosomal background of cancerous mutations using a long-read sequencer

In our previous study detecting cancerous complex SVs, we performed whole-genome sequencing of lung cancer clinical samples using PromethION. In this study, its depth and quality was substantially enriched and we conducted the phasing analysis in human lung cancer genomes. In addition, long read and short read RNA-seq was performed for transcriptome analysis.

• Type: Tumor vs. Matched-Normal
• Archiver: Japanese Genotype-phenotype Archive (JGA)