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Updated: Jul 16, 2025

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epiAneufinder从单细胞ATAC-seq数据中识别出副本编号的变化

Akshaya Ramakrishnan1, Aikaterini Symeonidi2,3, Patrick Hanel1,4

  • 1Institute of Computational Biology, Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany.

Nature communications
|September 20, 2023
PubMed
概括

EpiAneufinder分析单细胞ATAC-seq数据以检测单个细胞中的拷贝数变化 (CNA). 这种方法揭示了内异质性和克隆进化,没有额外的实验.

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相关概念视频

Comparing Copy Number Variations and SNPs02:26

Comparing Copy Number Variations and SNPs

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.
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...
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