Complete analysis of genomic architecture
through long-read sequencing with Oxford Nanopore® technology.
Whole Genome Sequencing (WGS) provides a complete view of the genomic architecture, including the characterization of repetitive regions, complex structural variants (SV), and polymorphisms at the single-nucleotide (SNP) level.
Thanks to long-read sequencing offered by Oxford Nanopore technology, it is possible to analyze with greater continuity genomic regions that are difficult to resolve with short-read fragment-based technologies. This approach also enables de novo assembly of complex genomes and phasing of allele-specific haplotypes.
Sequencing is performed on the Oxford Nanopore Technologies® platform, enabling direct analysis of DNA molecules and ultra-long read generation.
Learn more on the dedicated Nanopore Sequencing → page.
Complete coverage of the entire genome, applicable to non-model organisms as well.
Sequencing of cell-free circulating DNA for non-invasive studies.
Targeted analysis of specific genomic regions.
We offer a fully end-to-end service tailored to research needs.
Our team supports the client from experimental design consultation through to biological interpretation of results.
Management of the complete library workflow: extraction of nucleic acids, quality control of the sample, library preparation and sequencing on the PromethION platform.
The bioinformatics pipeline includes base calling, quality check and read trimming, spatial read analysis, assembly and variant calling.
We can manage the upload of raw data to public repositories and provide support for biological interpretation of results.
Probiomics genomic sequencing services are exclusively dedicated to research projects in academic, industrial and biotechnological settings.
Study of structural variants, rare mutations and complex genomic alterations.
Genomic analysis of microbial communities and identification of microorganisms in environmental or experimental samples.
De novo assembly and genomic characterization of species with no completely resolved reference genome.
Analysis of cell-free DNA (cfDNA) circulating DNA and study of molecular biomarkers in research projects.
Multidisciplinary expertise in genomics, bioinformatics and molecular biology.
Full support from experimental planning through to delivery of results.
Oxford Nanopore Select platform for whole-genome long-read sequencing.
We collaborate with academic groups, clinics and industry to adapt the workflow to each research need.
Probiomics supports genomic research projects through complete sequencing and data analysis workflows,
from experimental planning to biological interpretation of results.
Tell us briefly about your project or analytical need.
Our scientific team will evaluate your request and get back to you.
Tell us briefly about your project or analytical need.
Our scientific team will evaluate your request and get back to you.
