Comprehensive detection of variants in unsolved rare disease cases with PacBio HiFi readsWilliam J. Rowell,Aaron M. Wenger, Roberto Lleras, Matthew H. McLoughlin, Benjamin M. Moskowitz,Emily Farrow,Neil Miller,Isabelle Thiffault,Shreyasee Chakraborty,Christine Lambert,Primo Baybayan,Tomi PastinenEUROPEAN JOURNAL OF HUMAN GENETICS(2022)引用 0|浏览33暂无评分AI 理解论文溯源树样例生成溯源树,研究论文发展脉络Chat Paper正在生成论文摘要