NextSeqシリーズの柔軟なパワーを活用するためのリソース

注目のNextSeq文献、製品資料、ビデオ、およびウェビナー

NextSeqシリーズリソース

Clonal evolution and resistance to EGFR blockade in the blood of colorectal cancer patients.

Nat Med   2015

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Pancreatic ß cell enhancers regulate rhythmic transcription of genes controlling insulin secretion.

Science 350 aac4250 2015

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An oncogenic MYB feedback loop drives alternate cell fates in adenoid cystic carcinoma.

Nat Genet 48 265-72 2016

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製品選択ツールおよび実験計画ツール
製品選択ツールおよび実験計画ツール

お客様のニーズに最適な製品を選択し、実験を計画するのに役立つインタラクティブなツールをご紹介します。

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NextSeq 500 User Guide

This guide contains an overview of instrument components and instructions for operating and maintaining the NextSeq 500.

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NextSeq Series Site Prep Guide

This guide contains lab specifications and requirements for preparing a site for the NextSeq 500 and NextSeq 550 systems.

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Sequencing Online Training

Online Illumina sequencing courses are free, interactive, and available any time.

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Personalized Training Workflow Selection Tool

This tool will help you determine the best hands-on sequencing training for your needs based on your area of interest, application, library preparation kit, and platform.

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Sequencing Coverage

Sequencing coverage describes the average number of NGS reads that align to known reference bases. Coverage requirements vary by application.

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Quality Scores

Additional information about sequencing quality scores, how they are calculated, and the relationship between quality score and base call accuracy.

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NextSeq Series Documentation

System guides, related application and tech notes, and other supporting documentation for the NextSeq Series.

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Sequencing Troubleshooting Tips

These short videos provide expert tips for common sequencing issues such as overclustering and inconsistent quantitation.

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Custom Protocol Selector

The Custom Protocol Selector enables you to generate your own customized documentation, specifically tailored to your experiment.

Create Protocols
Deeper Insights on RNA Sequencing
Deeper Insights on RNA Sequencing

このラボでは、NextSeq 500システムのRNAシーケンスによって最先端のウイルス学研究が促進され、単なる遺伝子発現を超える深い洞察が得られています。

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Deciphering the Role of Long Non-Coding RNA in Cancer

Researchers are using RNA-Seq to reveal how lncRNAs could be used to identify, measure, and treat cancer.

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NGS Panels Demonstrate Value in Brain Tumor Studies

TruSight Tumor 170 accurately identifies diffuse glioma genetic markers, supporting use in tumor characterization for clinical research studies.

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Higher Data Quality and Expanded Applications
Higher Data Quality and Expanded Applications

NGS advancements help you harness the power of a seamless workflow solution for your lab.

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Transition to an RNA-Seq Workflow Solution
Transition to an RNA-Seq Workflow Solution

See how easy it is to transition to next-generation RNA sequencing with a step-by-step guide, from library prep to data analysis.

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Somatic Variant Discovery in Cancer Genomics
Somatic Variant Discovery in Cancer Genomics

Learn how researchers are using the NextSeq Series to continue to discover the biology of cancer and translate discoveries.

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RNA Sequencing on the NextSeq Series
RNA Sequencing on the NextSeq Series

Demonstration of how the NextSeq Series makes the advantages of RNA-Seq more accessible than ever before.

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