Đang chuẩn bị liên kết để tải về tài liệu:
SubPatCNV: Approximate subspace pattern mining for mapping copy-number variations
Đang chuẩn bị nút TẢI XUỐNG, xin hãy chờ
Tải xuống
Many DNA copy-number variations (CNVs) are known to lead to phenotypic variations and pathogenesis. While CNVs are often only common in a small number of samples in the studied population or patient cohort. |