Whole Genome
Sequencing
Comprehensive genomic analysis for your genome of interest
What is Whole
Genome Sequencing?
Whole Genome Sequencing (WGS) provides a complete, high-resolution view of an organism’s DNA, enabling the detection of both common and rare genetic variants across the entire genome. This powerful approach supports a wide range of applications from identifying disease-associated mutations and molecular biomarkers to advancing species discovery and evolutionary research.
We utilize a comprehensive suite of short-read and long-read sequencing platforms to deliver flexible Whole Genome Sequencing (WGS) solutions. This technological versatility allows us to expertly handle diverse projects involving human, animal, plant, and microbial genomes, as well as a variety of sample types, ensuring precision and speed.
We support both resequencing ideal for detecting variations such as SNPs, CNVs, and structural variants relative to a reference genome—and de novo sequencing, which enables the assembly and analysis of novel or uncharacterized genomes from scratch.
Whole Genome Sequencing at Admera Health
Human WGS
Analyze human genomes with high-throughput sequencing on Illumina NovaSeq X Plus, NovaSeq 6000, NextSeq, MiSeq, or PacBio Revio. Customizable sequencing depths and coverages available to suit your project’s scale.
CLIA WGS
Research-use only WGS service for researchers who require clinical-quality deliverables with an added layer of confidence.
Non-human WGS
Complete genomic profiling across diverse species to support research in agriculture, biodiversity, and studies for model and non-model organisms.
Low-Pass WGS
High-throughput WGS at a lower sequencing coverage. Cost-effective variant detection commonly used on genome-wide association studies, population-scale genotyping, polygenic risk scoring, and more.
De Novo Sequencing
Assemble and analyze entire genomes from scratch, essential for studying novel organisms, structural variants, and reference-free genomics research.
ddRAD-seq
Double Digest Restriction-site Associated DNA Sequencing is a cost-effective high-throughput method used for SNP discovery and genotyping, ideal for genetic mapping, population genomics, and evolutionary biology.
Whole Genome Sequencing Applications
Identify genetic variations that are causally linked to diseases to reveal new points of therapeutic intervention.
Discover Novel Drug Targets
Pinpoint specific genetic mutations and variants that are responsible for the onset and progression of diseases
Uncover Disease-Driving Mutations
Personalize Disease Treatment
Tailor medical therapies and drug dosages to an individual's unique genetic makeup for improved efficacy
Reconstruct the complete genetic blueprint of organisms with no existing reference genome for research purposes
Assemble Novel Genomes
Get the Most out of Your Study
Maximize your project’s potential with advanced analysis solutions. Our team of expert bioinformaticians curate pipelines tailored to your project’s experimental design.
See WGS in Action
Admera Health provides comprehensive support for all projects, and delivers publication-ready data. Discover how researchers are using Admera Health to advance their projects.