相关实验视频

Updated: Jul 5, 2025

Rare Event Detection Using Error-corrected DNA and RNA Sequencing
10:36

Rare Event Detection Using Error-corrected DNA and RNA Sequencing

Published on: August 3, 2018

12.1K

超敏感的分子残留疾病检测通过全基因组测序与一次性读取错误校正

Xinxing Li, Tao Liu, Antonella Bacchiocchi

    medRxiv : the preprint server for health sciences
    |January 23, 2024
    PubMed
    概括

    在无细胞DNA分析中,AccuScan技术显著减少了全基因组测序错误. 这一突破使分子残留疾病 (MRD) 的高度敏感检测成为可能,并预测多种癌症类型的复发.

    更多相关视频

    Ultra-long Read Sequencing for Whole Genomic DNA Analysis10:34

    Ultra-long Read Sequencing for Whole Genomic DNA Analysis

    Published on: March 15, 2019

    22.8K
    Detection of Rare Mutations in CtDNA Using Next Generation Sequencing11:11

    Detection of Rare Mutations in CtDNA Using Next Generation Sequencing

    Published on: August 24, 2017

    16.8K

    相关概念视频

    Next-generation Sequencing03:00

    Next-generation Sequencing

    The first human genome sequencing project cost $2.7 billion and was declared complete in 2003, after 15 years of international cooperation and collaboration between several research teams and funding agencies. Today, with the advent of next-generation sequencing technologies, the cost and time of sequencing a human genome have dropped over 100 fold.
    Next-Generation Sequencing Methods
    Although all next-generation methods use different technologies, they all share a set of standard features....
    88.8K