Whole-Genome Sequencing (WGS)

Next-generation sequencing

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Instruments available

Setups offered

Sample types

Data analysis support

What is short-read sequencing?

Short-read sequencing is a widely adopted high-throughput DNA and RNA sequencing method that generates large volumes of highly accurate data using short sequence reads, typically 75 to 300 base pairs in length. This technology is optimal for variant calling, gene expression profiling, microbial identification, and high-throughput screening of genetic elements.
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Instruments available

Illumina iSeq 100

Compact benchtop sequencer for smaller-scale applications and pilot studies.
Illumina iSeq 100

Element Biosciences AVITI

Mid- to high-throughput sequencer with exceptional accuracy and cost-efficiency.  


Partner Access

OHMX.bio also offers sequencing services via established partners using:
    • Element Biosciences AVITI 24
    • Illumina NovaSeq X
NovaseqX_AVITI24

Setups offered

OHMX.bio supports a wide range of short-read NGS setups:

Whole Genome Sequencing (WGS)

Broad overview of genomic content, ideal for identifying SNPs, indels, and structural variants.

Whole Exome Sequencing (WES)

Focused on the protein-coding regions of the genome, suited for variant discovery in clinical research.

RNA Sequencing (RNA-Seq)

Quantification of gene expression, detection of alternative splicing, and transcript discovery.

Small RNA Sequencing

Characterization of microRNAs and other small regulatory RNAs.

Methylation Sequencing (Bisulfite-seq)

Analysis of DNA methylation patterns at base-pair resolution.

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Sample types

OHMX.bio processes a wide variety of DNA and RNA samples. For full sample submission guidelines, please refer to our sample requirements page.

Advantages

  • High base accuracy (>90%Q40 for AVITI)
  • High throughput and scalability
  • Well-established protocols and analysis pipelines
  • Cost-effective for large sample sets
  • Suitable for discovery and validation workflows

Common Applications

  • Variant detection in clinical and research samples
  • Transcriptomics (gene expression profiling)
  • Tumor heterogeneity analysis
  • Epigenetic profiling
  • Targeted panel sequencing
  • Biomarker discovery and validation

Data analysis support

Our in-house bioinformatics team ensures high-quality data analysis, including raw data QC, alignment, variant calling, differential expression, and custom reporting. Scientists and bioinformatics experts work closely together to ensure accurate interpretation and actionable insights.
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Partner with OHMX.bio

Whether you are conducting fundamental research, developing novel therapeutics, or advancing clinical diagnostics, OHMX.bio’s lab- and bio-IT solutions are here to support your goals. Our commitment to innovation, quality, and client success makes us the ideal partner for generating advanced biological insights.
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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.

Frequently asked questions about next-generation sequencing

Short-read sequencing is a high-throughput DNA and RNA sequencing method that generates highly accurate reads typically between 75 and 300 base pairs in length. It is widely used for variant detection, gene expression profiling, microbial identification, epigenetic studies, and targeted sequencing. Its scalability and accuracy make it a cornerstone technology in genomics research and clinical studies.
OHMX.bio has several short- and long-read instruments in-house, adapted for small- and high-throughput projects, including Illumina based instruments, Element Biosciences instruments and Oxford Nanopore. This flexible instrument access allows scalability depending on project size and complexity.
OHMX.bio provides a comprehensive suite of Next-Generation Sequencing (NGS) applications, including Whole Genome Sequencing (WGS), Whole Exome Sequencing (WES), and high-resolution Transcriptomics. Our platform specializes in bridging the gap between DNA and protein through advanced Translatomics (Ribosome Profiling) and Single-Cell RNA sequencing, ensuring deep insights into cellular heterogeneity. We utilize a hybrid technology approach, leveraging both short-read (Illumina/Element) and long-read (Oxford Nanopore) platforms to support diverse research needs from epigenetics to microbiome profiling. This multi-omic capability is backed by expert bioinformatics pipelines designed to transform raw sequencing data into actionable biological discoveries.
Short-read sequencing provides high base accuracy, high throughput, and cost-effectiveness for large sample sets. Well-established protocols and validated bioinformatics pipelines ensure robust and reproducible data. This makes the technology suitable for both discovery research and validation studies.
OHMX.bio offers in-house bioinformatics services, including raw data quality control, alignment, variant calling, differential expression analysis, and custom visualisation and reporting. Scientists and bioinformaticians collaborate closely to translate sequencing results into actionable biological insights.

Our publications using short-read sequencing solutions

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