Identifies the changes in gene expression for cell fate determination
Enables the study of anthropology, evolution and human migration
Rapidly identify genes or SNPs of interest for identification
Studies on agriculture, livestock breeding and bioprocessing
Detection and treatment of diseases, e.g. cancer and the genetic causes, and the role of gene regulation in diseases
We perform DNA sequencing and assemble a reference genome for your research.
We use existing RNA-Seq data or perform RNA sequencing in order to annotate a genome.
Import genomic data from non-model organisms into our Ortholog Explorer tool to easily find ortholog genes and pathways of interest.
We import genomic data into Tupac.bio Designer to allow you to quickly navigate genomic data and design constructs using the data.
Considering DNA sequencing or using genomic data for your research? Get in touch to discuss your research objectives.
Assembles highly repetitive genomes when short-read data is not sufficient. This allows for the assembly of more complete genomes with fewer contigs.
Nanopore sequencing processes the entire length of DNA fragment into the pore which provides a more complete view of genetic variants.
DNA chemical modification regulates genomic function. Epigenetic modifications can be detected by Nanopore sequencing.
Long-read Nanopore sequencing data allows for direct read-based phasing of genetic variation which is critical for human disease studies.
If you have any inquiries get in touch with us and we'll get back to you right away.