Optimized shallow whole-genome sequencing for large CNV detection in rare genetic disordersAnett Marais,Krishna Kumar Kandaswamy,Antonio Romito,Natalia Ordonez, Dan Diego Alvarez,Katja Bruesehafer,Volkmar Weckesser,Peter Bauer, Jonas MarcelloEUROPEAN JOURNAL OF HUMAN GENETICS(2022)引用 0|浏览1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