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Updated: Jul 26, 2025

Screening for Functional Non-coding Genetic Variants Using Electrophoretic Mobility Shift Assay EMSA and DNA-affinity Precipitation Assay DAPA
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Screening for Functional Non-coding Genetic Variants Using Electrophoretic Mobility Shift Assay EMSA and DNA-affinity Precipitation Assay DAPA

Published on: August 21, 2016

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VarDecrypt:一种新且易于使用的工具,用于探索和优先考虑整个exome测序数据中的变体

Mohammad Salma1,2, Elina Alaterre3, Jérôme Moreaux4,3,5

  • 1Institut de Génétique Moléculaire de Montpellier, Univ Montpellier, CNRS, Montpellier, France. mohammad.salma@igmm.cnrs.fr.

Epigenetics & chromatin
|June 13, 2023
PubMed
概括

VarDecrypt是一个新的基于网络的工具,简化了全外因子测序 (WES) 数据分析,以识别引起疾病的基因变异. 这个用户友好的应用程序帮助研究人员和临床医生从复杂的数据集中发现关键的遗传信息.

关键词:
患有急性白血病的人.生物信息学是一种生物信息学.疾病驱动基因是疾病的驱动基因.整体外基因组测序的测序

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Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease09:34

Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease

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Sequencing of the human genome has opened up several best-kept secrets of the genome. Scientists have identified thousands of genome variations that exist within a population. These variations can be a single nucleotide or a larger chromosomal variation.
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