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Updated: Jul 10, 2026

gDNA Enrichment by a Transposase-based Technology for NGS Analysis of the Whole Sequence of BRCA1, BRCA2, and 9 Genes Involved in DNA Damage Repair
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gDNA Enrichment by a Transposase-based Technology for NGS Analysis of the Whole Sequence of BRCA1, BRCA2, and 9 Genes Involved in DNA Damage Repair

Published on: October 6, 2014

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用NGS方法并行处理高质量,损坏或碎片化的输入材料,使用目标缩

Anna Lyander1,2, Anna Gellerbring2, Moa Hägglund2

  • 1Science for Life Laboratory, KTH Royal Institute of Technology, Clinical Genomics Stockholm, School of Engineering Sciences in Chemistry, Biotechnology and Health, Stockholm, Sweden.

PloS one
|May 29, 2024
PubMed
概括

下一代测序 (NGS) 库的准备是具有挑战性的,因为不同的DNA质量. 一个新的联合程序使得从各种样本类型中高效地准备DNA库,用于基因组学和诊断.

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Target Cell Pre-enrichment and Whole Genome Amplification for Single Cell Downstream Characterization10:12

Target Cell Pre-enrichment and Whole Genome Amplification for Single Cell Downstream Characterization

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相关概念视频

Long-patch Base Excision Repair01:02

Long-patch Base Excision Repair

Since the discovery of the two BER pathways, there has been a debate about how a cell chooses one pathway over the other and the factors determining this selection. Numerous in vitro experiments have pointed out multiple determinants for the sub-pathway selection. These are: