Đang chuẩn bị liên kết để tải về tài liệu:
SeqCNV: A novel method for identification of copy number variations in targeted next-generation sequencing data

Không đóng trình duyệt đến khi xuất hiện nút TẢI XUỐNG Tải xuống

Targeted next-generation sequencing (NGS) has been widely used as a cost-effective way to identify the genetic basis of human disorders. Copy number variations (CNVs) contribute significantly to human genomic variability, some of which can lead to disease. However, effective detection of CNVs from targeted capture sequencing data remains challenging. |