PGVDA:,使.

Sanghyun Shon1, Younhee Ko2, Hojin Yoon1,3

  • 1Department of Biomedical Informatics, Korea University College of Medicine, 73 Goryeodae-ro, Seongbuk-gu, Seoul 02841, Republic of Korea.

PubMed
概括

本研究引入了一种机器学习方法,使用基于途径的遗传变异剂量平均值 (PGVDA) 来通过分析生物途径内的遗传变异来区分神经肌肉结合障碍 (NMD) 和炎症性多神经病变 (IPN).

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