[3LBA-139] An Evaluation of NGS Platforms in Large-Scale Clinical Whole-Exome Sequencing Analyses for Rare and Undiagnosed Diseases
Genetic Disorders, Rare and Undiagnosed Diseases, Large-Scale Clinical Whole-Exome Sequencing, Next Generation Sequencing, IRUD
This archive has moved to the member page of The Molecular Biology Society of Japan.
Members can access the abstracts via links at the member page of the sites.
Please feel free to contact the journal offices for any inquiries.