Đang chuẩn bị liên kết để tải về tài liệu:
Exome sequencing in one family with gastric- and rectal cancer

Không đóng trình duyệt đến khi xuất hiện nút TẢI XUỐNG

Heritable factors are well known to increase the risk of cancer in families. Known susceptibility genes account for a small proportion of all colorectal cancer cases. The aim of this study was to identify the genetic background in a family suggested to segregate a dominant cancer syndrome with a high risk of rectal- and gastric cancer. |

TÀI LIỆU LIÊN QUAN

Whole exome sequencing pipeline evaluation and mutation detection in esophageal cancer patients

Performance assessment of variant calling pipelines using human whole exome sequencing and simulated data

Identification of a de novo mutation in KRT5 gene underlying epidermolysis bullosa simplex by whole exome sequencing in a Vietnamese patient

Opportunities and challenges of whole-genome and exome sequencing

A new massively parallel nanoball sequencing platform for whole exome research

Variant detection sensitivity and biases in whole genome and exome sequencing

Shared genetic susceptibilities for irritable bowel syndrome and depressive disorder in Chinese patients uncovered by pooled whole-exome sequencing

Comparative study of whole exome sequencing-based copy number variation detection tools

Effective filtering strategies to improve data quality from population-based whole exome sequencing studies

Whole exome sequencing in the rat
Đã phát hiện trình chặn quảng cáo AdBlock
Trang web này phụ thuộc vào doanh thu từ số lần hiển thị quảng cáo để tồn tại. Vui lòng tắt trình chặn quảng cáo của bạn hoặc tạm dừng tính năng chặn quảng cáo cho trang web này.