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Updated: Jun 10, 2026

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations
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A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations

Published on: December 1, 2017

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基因组测序对于预测先天性心脏手术后的结果至关重要

W Scott Watkins, E Javier Hernandez, Thomas Miller

    medRxiv : the preprint server for health sciences
    |May 15, 2024
    PubMed
    概括

    在人工智能的帮助下,基因组测序可以预测先天性心脏缺陷 (CHD) 患者的手术结果. 识别有害的遗传变异可以改善手术后不良事件的风险评估.

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    Author Spotlight: Nuclei Isolation from Mouse Cardiac Progenitor Cells for Epigenome and Gene Expression Profiling at Single-Cell Resolution

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    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.