Products
QIAseq Immune Repertoire RNA Library Kits are intended for molecular biology applications. These products are not intended for the diagnosis, prevention, or treatment of a disease.
QIAseq Targeted RNA Panel Human TCR (96)
Cat no. / ID. 334665
Includes enzymes, buffers and TCR-alpha, TCR-beta, TCR-gamma and TCR-delta panels
Features
- Unique Molecular Indices (UMI) ensure accurate sequencing results
- Online data analysis through GeneGlobe
- Includes QIAseq Beads for reaction cleanup
- Automation-friendly protocol for human or mouse samples
- QIAseq Sample Indices ordered separately to multiplex up to 384 samples
Product Details
The QIAseq Immune Repertoire RNA Library Kits use Unique Molecular Indices (UMI) with gene-specific primers to target specific RNAs for NGS sequencing. Each unique panel is carefully designed and laboratory-verified for sequencing performance with a UMI-aware alignment software for maximum sequencing performance and accurate results. The Human and Mouse T-cell Receptors Panel is used for sequencing the V(D)J region of the alpha, beta, delta and gamma genes, including the CDR3 regions. Online analysis through the GeneGlobe Data Analysis Center provides key sequencing QC metrics, as well as the frequency and identity of each clonotype sequenced.
This kit has been upgraded to the QIAseq Targeted RNA-seq Panel for T-cell Receptor. We recommend starting new projects with the upgraded kits.
Performance
Comprehensive view of the T-cell immune repertoire
The heatmaps allow for easy identification of enriched clonotypes across the sample. This figure shows the major clonotype of the Jurkat cell, as well as the diversity of the PBMC background. The data analysis included with the purchase of the QIAseq Immune Repertoire T-cell receptor panels includes an online portal that seamlessly integrates with Illumina BaseSpace and provides primary read mapping, UMI demultiplexing and reports on sequencing performance, TCR chain usage, CDR3 peptide sequence and length distributions, together with rarefaction and V/D/J usage heat maps.Sensitive to at least 0.01%
RNA from Jurkat cells was spiked into RNA extracted from peripheral blood mononuclear cells (PBMCs; Precision Medicine) at 10%, 1%, 0.1% and 0.01% and used to make an RNA-seq library. Table 1 shows the number of raw reads and the demultiplexed unique captures (UMIs) per Jurkat TCR-alpha and TCR-beta clonotype. Even when present at only 0.01%, the Jurkat RNA is readily quantifiably identified. For data analysis, UMIs and Raw Reads are used to ensure high precision around each clonotype sequence identified.
| Chain | % Jurkat cells | Rank | Reads | UMIs |
|---|---|---|---|---|
| TCR-alpha | 10 | 1 | 751,749 | 107,150 |
| 1 | 1 | 146,959 | 20,692 | |
| 0.1 | 1 | 10,708 | 1,742 | |
| 0.01 | 10 | 1,306 | 217 | |
| TCR-beta | 10 | 1 | 383,594 | 40,943 |
| 1 | 1 | 5,920 | 7,541 | |
| 0.1 | 2 | 5,401 | 620 | |
| 0.01 | 61 | 457 | 60 |
Principle
By using UMIs, the QIAseq Immune Repertoire RNA Library Kit Panel eliminates PCR duplicates and minimizes artifacts that may arise during the library preparation process or during the sequencing run. This ensures sensitive, accurate and unbiased quantification of the number of TCR transcripts captured and sequenced.
The QIAseq Immune Repertoire RNA Library Kit relies on a highly efficient, TCR-specific cDNA synthesis reaction, ligation of sample index adapters containing UMIs and TCR gene-specific primer enrichment for sensitive TCR clonotype and diversity assessment. Each kit contains species-specific TCR reverse transcriptase and enrichment panel primers, together with QIAseq reaction cleanup beads and library reagents. The QIAseq Immune Repertoire RNA Library Kit is designed to enrich TCR α, β, γ and σ subunits using 10–1000 ng RNA from human or mouse samples.
The QIAseq Immune Repertoire RNA Library Kit relies on a highly efficient, TCR-specific cDNA synthesis reaction, ligation of sample index adapters containing UMIs and TCR gene-specific primer enrichment for sensitive TCR clonotype and diversity assessment. Each kit contains species-specific TCR reverse transcriptase and enrichment panel primers, together with QIAseq reaction cleanup beads and library reagents. The QIAseq Immune Repertoire RNA Library Kit is designed to enrich TCR α, β, γ and σ subunits using 10–1000 ng RNA from human or mouse samples.
Procedure
The QIAseq Immune Repertoire RNA Library Kit relies on a highly efficient, TCR-specific cDNA synthesis, TCR gene-specific primer enrichment and molecular indexing for accurate and sensitive TCR clonotype and diversity assessment (see figure " QIAseq Immune Repertoire RNA Library workflow"). TCR reverse transcriptase and enrichment panel primers are provided, together with library reagents.
cDNA synthesis
RNA samples are first reverse transcribed into cDNA with TCR-specific RT primers. Subsequently, second-strand synthesis occurs, which generates double-stranded cDNA (ds-cDNA). This ds-cDNA is then end-repaired and A-tailed in a single-tube protocol.
UMI assignment
Prior to target enrichment and library amplification, each original cDNA molecule is assigned a UMI by ligating an adapter containing a 12-base fully random sequence (i.e., the UMI) to the ds-cDNA. Statistically, this process provides 4^12 possible indices per adapter, and each DNA molecule in the sample receives a unique UMI sequence. In addition, this ligated adapter also contains the first sample index.
Target enrichment and final library construction
Following UMI assignment, target enrichment is performed to ensure that TCR cDNA molecules are sufficiently enriched in the sequenced library. For enrichment, ligated cDNA molecules are subjected to targeted PCR using one TCR constant-region-specific primer and one universal primer complementary to the adapter. A universal PCR is ultimately carried out to amplify the library and introduce platform-specific adapter sequences, as well as additional sample indices.
Applications
This kit provides a solution for immune repertoire sequencing from RNA.
Supporting data and figures
CDR3 Length Plots are Shown for Each Receptor in from a Single Sample.
Resources
Kit Handbooks (1)
Safety Data Sheets (1)
Certificates of Analysis (1)
User Manuals (1)
Publications
PD-1 and TIGIT coexpression identifies a circulating CD8 T cell subset predictive of response to anti-PD-1 therapy.
J Immunother Cancer; 2020; 8 (2) 2020 Nov PMID:33188038
TCR Analyses of Two Vast and Shared Melanoma Antigen-Specific T Cell Repertoires: Common and Specific Features.
Front Immunol; 2018; 9:1962 2018 Aug 30 PMID:30214446
Diagnosing Viral Infections Through T-Cell Receptor Sequencing of Activated CD8+ T Cells.
J Infect Dis; 2024; 229 (2):507-516 2024 Feb 14 PMID:37787611
Evidence of premature lymphocyte aging in people with low anti-spike antibody levels after BNT162b2 vaccination.
iScience; 2022; 25 (10):105209 2022 Sep 26 PMID:36188190
Preexisting memory CD4 T cells in naïve individuals confer robust immunity upon hepatitis B vaccination.
Elife; 2022; 11 2022 Jan 25 PMID:35074048
FAQ
What are the major differences between QIAseq Targeted RNA Panel TCR kit and previous QIAseq Immune Repertoire RNA library kit?
Do you expect BCR panels with the QIAseq Targeted RNA Panel TCR kit technology to be available in the coming future?
Have you tested the panels at very low input such as 10 pg input? What is the expected performance at lower input.
What software do you use to analyze data?
Does QIAGEN have validated automation script for instrument like Hamilton NGS STAR?
What is the lowest amount of RNA input I can use?
Is this workflow compatible with sequencers other than those from Illumina?
What is the best sample QC method to use for the QIAseq Targeted RNA Panel TCR kit workflow?
Why do we recommend long reads kit even you don’t report full length TCR information?
Can libraries from different product line be mixed and run together in the same run?