関連する実験動画

Updated: Jun 21, 2026

Automating ChIP-seq Experiments to Generate Epigenetic Profiles on 10,000 HeLa Cells
08:34

Automating ChIP-seq Experiments to Generate Epigenetic Profiles on 10,000 HeLa Cells

Published on: December 10, 2014

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Cell2Read：ヒト細胞懸濁液からシーケンシング準備済みDNAライブラリを生成するための自動ワークフロー

Kathryn Whitehead1, Sarah Planchak1, Trinity Williams1

  • 1Center for Biomedical Engineering, School of Engineering, Brown University, Providence, RI 02912, United States.

Biology methods & protocols
|December 30, 2025
PubMed
まとめ

Cell2Readは、細胞溶解および次世代シーケンシング（NGS）用サンプル調製を自動化し、わずか1500個の細胞から高品質DNA分析を可能にします。この新しい方法は、ゲノム研究および診断に不可欠な、多様な細胞タイプに対して再現性の高い結果を保証します。

キーワード:
DNA抽出自動化自動DNAライブラリ調製がん細胞検出細胞溶解ハイスループットゲノミクス低入力シーケンシング腫瘍診断

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Author Spotlight: An Integrated Workflow to Study the Promoter-Centric Spatio-Temporal Genome Architecture in Scarce Cell Populations11:36

Author Spotlight: An Integrated Workflow to Study the Promoter-Centric Spatio-Temporal Genome Architecture in Scarce Cell Populations

Published on: April 21, 2023

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Author Spotlight: Enhancing Drug Discovery - Development of Automated, Standardized Protocols for Nuclei Extraction from Frozen Tissues07:12

Author Spotlight: Enhancing Drug Discovery - Development of Automated, Standardized Protocols for Nuclei Extraction from Frozen Tissues

Published on: July 28, 2023

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関連する概念動画

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.
RNA-seq03:21

RNA-seq

RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases. 
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while microarray-based...