Introduction to Total RNA Sequencing
Whole-transcriptome analysis with total RNA sequencing (RNA-Seq) detects coding plus multiple forms of noncoding RNA. Total RNA-Seq can accurately measure gene and transcript abundance, and identify known and novel features of the transcriptome.
Total RNA-Seq provides optimal coverage in normal or low-quality samples. Species-specific ribosomal RNA probes can efficiently remove abundant RNA species. This leaves both fragmented and intact transcripts of interest for library capture.
Advantages of Total RNA Sequencing
Total RNA-Seq analyzes both coding and multiple forms of noncoding RNA for a comprehensive view of the transcriptome.
- Captures both known and novel features
- Allows researchers to identify biomarkers across the broadest range of transcripts
- Enables a more comprehensive understanding of phenotypes of interest
- Allows profiling of the whole transcriptome across a wide dynamic range
Transitioning from Whole-Genome Arrays to Total RNA-Seq
Dr. Avrum Spira, a pulmonary and critical care physician at Boston University Medical Center, started
a lab with the goal of analyzing samples with whole-genome gene expression arrays, to study
potential biomarkers for pulmonary disorders. Learn how Spira’s lab uses total RNA-Seq to uncover
novel and rare transcripts that may not be detectable on expression arrays.
Read Case Study.
Deciphering the Role of Long Non-Coding RNA in Cancer
Researchers at Biogazelle are using RNA-Seq to reveal how lncRNAs can be specific to cell types. They discovered that silencing certain lncRNAs can help destroy cancer cells.
Read Interview
Total RNA Sequencing Workflow
Illumina sequencing by synthesis (SBS) chemistry is the most widely adopted next-generation sequencing (NGS) technology, producing approximately 90% of global sequencing data.*
In addition to high-quality data, Illumina offers integrated whole-transcriptome sequencing workflows that simplify the entire process, from library preparation to data analysis and biological interpretation.
Library Prep for Total RNA-Seq
Our enhanced RNA-Seq library prep portfolio includes removal of abundant rRNA, so you can focus on high-value portions of the transcriptome.
Learn MoreRNA シーケンス検討事項
遺伝子発現プロファイリング、ターゲットRNA発現、small RNA解析、など、それぞれのRNA-Seq実験によって、必要とされるリード長や深度は異なります。このページでは、実験において考慮すべき点をレビューしています。実験計画にご活用ください。
詳細はこちら
Using NGS to Study Rare Undiagnosed Genetic Disease
Whole-exome and transcriptome sequencing prove beneficial in uncovering mutations and pathways associated with rare disease
Learn MoreFeatured Products
NextSeq 1000 & 2000 Systems
Groundbreaking benchtop sequencers allow you to explore new discoveries across a variety of current and emerging applications, with higher efficiency and fewer restraints.
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Illumina Ribo-Zero Plus rRNA Depletion Kit
The stand-alone Illumina Ribo-Zero Plus kit allows for ribosomal RNA removal in human, mouse, rat, and bacterial samples.
Learn More
Illumina Stranded Total RNA Prep with Ribo-Zero Plus
Rapid library preparation from a broad range of sample types for studying the coding and non-coding transcriptome with unparalleled study flexibility.
Learn MoreRelated Solutions
Cancer Research: Gene Expression Studies
Monitoring gene expression changes in both coding and noncoding RNA biomarkers with total RNA-Seq can help researchers understand which variants affect tumor classification and progression. Learn more about cancer RNA-Seq.
Agrigenomics: Deep Transcriptome Sequencing
Plants have large, repetitive genomes, which can make it difficult to sequence weakly expressed genes. Ultradeep RNA sequencing can facilitate analysis of these genes. Learn more about plant sequencing.
Complex Disease Biomarker Identification
Total RNA-Seq allows complex disease researchers to study coding and multiple forms of noncoding RNA in a single analysis, providing visibility to a broad range of potential disease-associated biomarkers. Learn more about complex disease research.
RNA-Based Drug Response Biomarker Discovery
Find out how to utilize RNA-Seq to identify novel RNA-based drug response biomarkers. Access resources designed to help new users adopt this application. Learn more about RNA biomarker analysis for drug development.
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Additional Resources
RNA-Seq データ解析
ユーザーフレンドリーなソフトウェアツールが、バイオインフォマティクスの経験がなくても、生物学者のためのmRNA-Seqデータ解析を簡素化させます。
低クオリティと FFPE サンプルのための RNA-Seq
ホルマリン固定パラフィン包埋（FFPE)および低クオリティサンプルのRNA-Seqにより、疾患研究のための価値のある情報をもたらします。
ペアエンド RNA シーケンス
ペアエンドRNA-Seqにより融合遺伝子や新規スプライスアイソフォームの特徴づけなどの探索アプリケーションを可能にします。
RNA-Seq と NextSeq シリーズ
NextSeqシリーズのシーケンスシステムはコスト効率的なRNA-Seqソリューションを手軽に手にすることができます。
*Data calculations on file. Illumina, Inc., 2015