测序方法探索工具
Use this interactive tool to explore experimental NGS library prep methods compiled from the scientific literature. The tool includes a subset of methods from the review articles and posters below. New methods will be added as they become available.利用此交互式工具来探索汇编自科学文献的实验性NGS文库制备方法。该工具包含来自如下综述文章、海报的各类方法和新方法（如可用）。
获取工具
测序方法海报
查看与边合成边测序技术兼容的DNA、RNA和单细胞库制备技术的原理图。还可查看Illumina文库制备试剂盒实验方案的简图。
Featured Method
scTrio-Seq
scTrio-Seq can analyze genomic CNVs, the DNA methylome, and the transcriptome of an individual mammalian cell simultaneousl. This approach is an extension of previous methods, such as scMT-seq.
Pros
- Accurately analyzes the mechanism by which the transcriptome, genome, and DNA methylome regulate each other
- CNVs can be identified reliably using scRRBS data
Cons
- Lower transcriptome coverage than scMT-seq1
- Results in 3'-biased transcriptome
方法指南
该指南提供了您需要的全部信息，包括用于文库制备的BeadChip芯片、测序仪选择和分析。为您的实验室选择较佳工具。
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Additional Resources
Create Custom Protocols
Generate custom sequencing protocols tailored to your Illumina instrument and experimental requirements.
Library Prep and Array Kit Selector
Find the right kit for your lab, study, and application.
Flexible High-Throughput Sequencer
The NovaSeq System offers scalable throughput and flexibility for virtually any genome, sequencing method, and scale of project.
Get the Illumina DNA Prep Advantage
A fast, integrated workflow for a wide range of applications, from human whole-genome sequencing to amplicons, plasmids, and microbial species.