Sequencing Data Generation
Biomiz can help you find whole genome sequencing experiments from the most convenient and cost-effective sequencing service provider. We evaluate the best offers from different providers worldwide to provide you with the best deal. A simplified and clear management of the process allows you to get sequencing data faster and easier.
If you already have the data, we may skip this phase and move straight to bioinformatics data
- THE RIGHT NGS SOLUTION
- THE BEST PRICE
- THE SIMPLEST WORKFLOW
// the workflow
Next/Third Generation Sequencing
(NGS) solution
THE RIGHT DESIGN
Tell us about your project and goals. We will discuss any whole genome sequencing services that would suit your needs.
THE BEST PRICE
We will take care of finding the most convenient and cost-effective whole genome sequencing provider to offer you an all-in-one solution.
THE SIMPLEST WORKFLOW
You can keep your focus on research while we manage the entire process, from sample shipment to data delivery.
Sequencing
Services
High-throughput sequencing methods enable the sequencing of nucleic acid sequences at different layers, from genomes to transcriptomes, with unprecedented power. The ability to generate large volumes of data greatly empowers genetic, biological, and medical research. The use of the latest NGS technologies, including the new Illumina® NovaSeq® X series and PacBio® Revio™ platforms, ensures you receive the highest quality data.
01
Genome Sequencing
- Whole Genome Sequencing (WGS). Comprehensive analysis of entire genome of an organism.
- Whole Exome Sequencing (WES). Target the exome to identify coding region variations efficiently.
- Targeted Sequencing. Focus on specific genes or regions of interest for in-depth study.
03
Transcriptome Sequencing
- RNA Sequencing (RNA-Seq). Measure gene expression by sequencing the entire transcriptome.
- Single-Cell RNA Sequencing (scRNA-Seq). Provide expression data at the single-cell level.
- smallRNA Sequencing (miRNA-Seq). Detect and quantifies small RNA molecules to study gene regulation.
02
Epigenome Sequencing
- Whole-Genome Bisulfite Sequencing (WGBS). Identify DNA methylation patterns across the entire genome.
- ChIP Sequencing (ChIP-Seq). Identify DNA-binding sites of proteins to study gene regulation.
- ATAC Sequencing (ATAC-Seq). Profile open chromatin regions to understand gene accessibility.
04
Metagenome Sequencing
- 16S/18S/ITS rRNA Sequencing. Characterize microbial communities based on ribosomal RNA gene regions.
- Shotgun Metagenomics. Offers high-resolution analysis of microbial diversity.
- Metatranscriptomics Sequencing. Capture the gene expression of microbial communities to understand functional dynamics.
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