Whole-Genome Sequencing (WGS)

Whole genome sequencing solutions

Unlock the full potential of genomic analysis with OHMX.bio’s advanced Whole Genome Sequencing (WGS) services. As experts in sequencing technologies, we provide tailored solutions to help you explore genetic variation, structural changes, and genome-wide patterns with high precision.
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What is whole genome sequencing?

Whole Genome Sequencing (WGS) is a next-generation sequencing (NGS) technology that enables comprehensive analysis of an organism’s complete DNA sequence. By sequencing the entire genome, researchers can identify mutations, structural variants, and other genetic features critical for understanding disease mechanisms, drug response, and variant analysis.
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Check our publications

Applications of whole genome sequencing

Genetic Disease Research

Identify pathogenic variants and explore the genetic basis of inherited disorders.

Oncology & Cancer Genomics

Detect somatic and germline mutations, copy number variations, and structural variations.

Pharmacogenomics

Understand how genetic variations influence drug metabolism and response for precision medicine.

Microbial and Pathogen Genomic

Characterize bacterial, viral, and fungal genomes for epidemiological studies and antimicrobial resistance research.

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OHMX.bio - Innovative omics solutions

Our sequencing platforms

OHMX.bio utilizes cutting-edge sequencing platforms, including Illumina platforms, the Element Biosciences AVITI sequencer for enhanced accuracy, and Oxford Nanopore for long-read sequencing. By combining short-read and long-read technologies, we offer de novo genome assemblies and high-resolution variant detection, providing unparalleled insight into genomic structure.
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Seamless bioinformatics integration

OHMX.bio offers comprehensive bioinformatics support, including variant analysis, annotation, and interpretation. Our expertise in de novo assembly and custom data analysis pipelines ensures high-quality, reproducible results. With years of experience handling diverse genomic datasets, we help you extract valuable insights for informed decision-making.

Let’s get in touch!

Are you curious about how we can work on your -omics challenges together? Fill out the form below!
Our experts will reply within 2 working days to freely discuss your omics project.

Our publications using our WGS services

  1. Iyer, Shruti V., Sara Goodwin, and William Richard McCombie. “Leveraging the power of long reads for targeted sequencing.” Genome Research 34.11 (2024): 1701-1718.
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