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Updated: Jun 17, 2026

Detection of Rare Genomic Variants from Pooled Sequencing Using SPLINTER
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Detection of Rare Genomic Variants from Pooled Sequencing Using SPLINTER

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对"EAP:一个基于云的多功能平台,用于对大型ChIP/ATAC-seq数据集进行有效的定量分析"的纠正 [Comput Struct Biotechnol J 27 (2025) 5220-5233]

Guangyong Zheng1,2, Haojie Chen1,3, Zhijie Guo1,3

  • 1Shanghai Institute of Nutrition and Health, Chinese Academy of Sciences, Shanghai, China.

Computational and structural biotechnology journal
|January 5, 2026
PubMed
概括

No abstract available in PubMed .

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

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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.