TruSeq RNA Access

TruSeq RNA Access

TruSeq RNA Access Library Prep kits convert total RNA into template molecules of known strand origin, followed by the targeted capture of coding RNA via sequence-specific capture probes, enabling cost-efficient, multi-plexed sequencing in both high and low-quality / FFPE samples.
Starting material: Compatible with a wide range of RNA input quality. Illumina recommends using the percentage of RNA fragments >200 nt distribution value (or DV200) as an indicator of RNA quality to ensure proper performance.

Catalog ID(s): Indexes Pre-Enrichment Multiplexing Enrichment Maximum Samples Per Kit
RS-301-2002 Set A: 12 indices 1-4 12/kit 48
RS-301-2001 Set B: 12 indices 1-4 12/kit 48

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Project Recommendations*
Species Compatibility Human
Recommended Illumina Instrument NextSeq 500 HiSeq 2500 (Dual Flow Cell) NovaSeq 6000 (Dual Flow Cell)
Recommended Samples per run 5–16 24–160 96 96 192
Run Mode Mid Output High Output Rapid Run High Output S1§ S2 S4
Max Recommended Read Length 2×75 bp 2×75 bp 2×75 bp 2×75 bp 2×100 bp
Recommended Secondary Analysis
  • TopHat Alignment BaseSpace App
  • Cufflinks Assembly & DE BaseSpace App
  • RNA Express v1.0 BaseSpace App
Recommended Down Stream Analysis
  • Genomatix Pathway
  • iPathway Guide

* Library prep is compatible with all Illumina instruments. Recommended instruments chosen based on typical output and analysis need for selected application.

† Currently limited by available index combinations.

‡ Based on 25M reads per sample.

§ NovaSeq S1 Reagent Kits are not currently available.