MGIEasy PCR-Free DNA Library Prep Set
The MGIEasy PCR-Free Library Prep Set is designed for whole-genome sequencing (WGS) library construction on MGI high-throughput sequencing platforms. Optimized for 80–200 ng of size-selected fragmented DNA, it converts DNA into high-quality, customized libraries.
Combined with the MGI DNBSEQ™ sequencer, this true PCR-free workflow eliminates PCR amplification, preventing error accumulation and delivering higher data accuracy. Ideal for researchers seeking reliable, high-fidelity WGS, the kit ensures robust performance across diverse genomic applications.
Product
| Product Name | Item Number | Component | Component Item Number |
|---|---|---|---|
| MGIEasy PCR-Free DNA Library Prep Set (16 RXN) | 1000013452 | Library and Circularization: MGIEasy PCR-Free DNA Library Prep Kit | 1000013456 |
| Adapter: MGIEasy PF Adapters-16 (tube) Kit | 1000013460 | ||
| Beads: MGIEasy DNA Clean Beads (8 mL) | 940-001596-00 | ||
| MGIEasy PCR-Free DNA Library Prep Set (96 RXN) | 1000013453 | Core library: MGIEasy PCR-Free DNA Library Prep Kit | 1000013457 |
| Adapter: MGIEasy PF Adapters-96 (plate) Kit | 1000013461 | ||
| Beads: MGIEasy DNA Clean Beads (50 mL) | 940-001594-00 |
Product Specification
| Product Name | MGIEasy PCR-Free DNA Library Prep Set |
| Application | Whole genome sequencing |
| Version | V1.1 |
| Configuration | 16 RXN (1000013452) and 96 RXN (1000013453) |
| Validity period | 9 months |
| Assay Time | ~3.5 hrs |
| Input Quantity | 80-200 ng fragmented DNA |
| Sample types | gDNA |
| Species Compatibility | Human, animals, plants, fungi, bacteria, metagenomics, etc. |
| Fragmentation Method | Sonication |
| Recommended Insert Size | 350-400 bp |
| Platform Compatibility | DNBSEQ-G400, DNBSEQ-G50, DNBSEQ-T7 |
| Recommended Read Length | SE100, PE100, PE150, PE200, SE400 |
Recommended Workflow
| Application | Library Preparation | Sequencing | Analysis |
|---|---|---|---|
| Human WGS sequencing (High depth) |
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Highlights
Compatible with Multiple Species
- Supports DNA from humans, animals, plants, bacteria, fungi, including blood, saliva, fresh tissue, mice, rice, E. coli, and metagenomic samples.
Fast, Simple, Automated Workflow
- Complete library preparation in 3.5 hours with size-selected DNA. The workflow is simple, automation-friendly, and avoids amplicon contamination.
No Amplification Error Accumulation
- By eliminating PCR amplification, the PCR-free workflow on MGI DNBSEQ™ platforms prevents error accumulation, delivering high-fidelity genome data.
Higher Coverage Uniformity & Variant Detection
- Reduces GC bias and improves coverage across the genome, including GC-rich, promoter, and repetitive regions, while enhancing sensitivity and accuracy for variant detection, especially indels.
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