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Maximize insights from minimal sample amounts
Working with single cells, cell populations or low-input DNA or RNA should not limit your ability to uncover a deeper view of the genome or transcriptome. QIAseq Single Cell Library Kits UDI can help you unravel genomic and transcriptomic details from single cells and limited amounts of nucleic acids. Prepare high-complexity whole genome or whole transcriptome libraries using a one-tube workflow with minimal hands-on time. Worried about bias? The PCR-free protocol means you can avoid a negative impact on library diversity from the loss of low-abundance transcripts or GC and length bias. Inclusion of Unique Dual Indices (UDI) minimizes sequencing artifacts due to “index hopping” on Illumina NGS instruments.Take the QIAseq challenge for single-cell and low-sample input NGS
QIAseq Single Cell RNA Library Kits UDI
- Start with single cells, cell populations or enrich for small RNA genomes or viruses
- Choose to focus on mRNAs or explore the transcriptome
- REPLI-g RNA amplification and PCR-free protocol reduces bias and provides greater reproducibility
- Includes Unique Dual Indices which ensure high-quality data from NovaSeq and patterned flow cells
- NGS-ready libraries from single cells in 5.5 h
Expand your knowledge by tuning into the webinar
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Take the fastest way to a single cell with Namocell's single-cell isolation technology.†
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Get started with single-cell whole genome library prep using QIAseq Single Cell DNA Library Kits UDI.
Sample to Insight solution for single-cell and low-input sequencing
Top 4 considerations for single-cell and low-input NGS
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1. Importance of isolation methodViability and gentle cell handling is mandatory to reveal accurate information from single cells
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2. Prerequisites for cell isolationCell type, sampling, isolation method and subsequent analysis are important attributes in a complete workflow and must be optimized
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3. REPLI-g amplificationQIAseq Single Cell REPLI-g amplification is a superior technology compared to PCR for studying the genome and transcriptome from single cells and low-input DNA or RNA
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4. Specific enrichment using QIAseq chemistryQIAseq Single Cell Library Kits UDI utilize a new buffer composition to allow specific enrichment of small genomes
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† This link takes you to an external third-party website owned and operated by Namocell, an independent third party unaffiliated with QIAGEN. This link is provided for convenience and informational purposes only. QIAGEN bears no responsibility for and makes no representations or warranties regarding the content of external websites. Please contact the external site directly for answers to any questions regarding its content.