Whole Genome
Sequencing
Designed to deliver reliable, superior outcomes for a range of uses, from simple research to intricate discoveries. The LeoNext WGS library preparation kit guarantees dependable, quick NGS library production throughout the whole genome with optimized methods and high-performance chemicals.
The user-friendly kit supports complicated genetic variation investigations, uncommon mutation detection, and thorough genomic analysis while cutting down on preparation time, minimizing input requirements, and performing consistently with challenging sample types.
Explore WGS →Prep Kit
Applications in Clinical & Research
Comprehensive genome-wide insights for complex biological questions.
Offers a thorough overview of the whole genome.
Identifies major structural variations (SVs), SNVs, Indels, and CNVs.
Finds variations that targeted techniques could overlook.
In a single experiment, it captures the whole range of cancer genomic changes, from point mutations to chromosomal rearrangements.
By collecting a wider range of variation pertinent to treatment response, it supports pharmacogenomics and drug trials.
Makes it possible to examine structural and noncoding variations in linkage areas in family illness pedigrees, going beyond a gene-centric approach.
Provides high-throughput microbial genome data to facilitate the construction of new genomes.
Variations
Indels
Variants
Key Features
Fast & Efficient
Optimized workflow for consistent results.
High Performance Chemistry
Reliable and reproducible library preparation.
Low Input
Works with as little as 100 pg of DNA.
Wide Sample Compatibility
Supports multiple sample types and challenging samples.
Comprehensive Coverage
Detects SNVs, Indels, CNVs and SVs.
Multi-Platform Support
Illumina, Thermo Fisher, MGI and Element Biosciences.
Parameter & Specifications
| Parameter | Detail |
|---|---|
| Format | DNA library preparation kit for short-read sequencing |
| Library prep time | 3–4 hours |
| Input range | 100 pg – 4 µg genomic DNA |
| Compatible sample types | Genomic DNA, cfDNA, ctDNA, FFPE DNA, ChIP DNA, Amplicons |
| Adapter ligation | High-efficiency ligation chemistry |
| Platform compatibility | Illumina, Thermo Fisher, MGI, Element Biosciences |
| Specification | Detail |
|---|---|
| Genome coverage | Whole genome (non-targeted) |
| Variant Types | SNVs, Indels, CNVs, Structural Variants (SVs) |
| Input DNA | 100 pg – 4 µg |
| Sample Types | Genomic DNA, cfDNA, ctDNA, FFPE DNA, ChIP DNA, Amplicons |
| Platform Compatibility | Illumina, Ion Torrent, MGI, Element Biosciences |
High-quality data for confident results
Experience superior coverage, accurate variant detection and reliable performance across a wide range of sample types and applications. The WGS solution delivers clean, consistent data to support research and genomic investigations.
& Uniformity
Detection
Reproducible
Streamlined Library Preparation Workflow
A simplified path from genomic material to sequencing data.
Extraction
High-quality genomic DNA from your samples.
Library Preparation
Optimized chemistry for maximum efficiency.
Sequencing
High-throughput platform compatibility.
Analysis
Reliable data for meaningful genomic insights.
Explore the complete genome.
Unlock broader genomic insights with a streamlined library preparation workflow.