DNA SEQUENCING SERVICES

We provide DNA sequencing using Nanopore and downstream bioinformatics analysis.

DNA SEQUENCING APPLICATIONS

Genetics

Identifies the changes in gene expression for cell fate determination

ANTHROPOLOGY

Enables the study of anthropology, evolution and human migration

Forensics

Rapidly identify genes or SNPs of interest for identification

Agriculture

Studies on agriculture, livestock breeding and bioprocessing

MEDICINE

Detection and treatment of diseases, e.g. cancer and the genetic causes, and the role of gene regulation in diseases

TUPAC.BIO SERVICES AND DOWNSTREAM SOFTWARE

Genome assembly

We perform DNA sequencing and assemble a reference genome for your research.

Genome annotation

We use existing RNA-Seq data or perform RNA sequencing in order to annotate a genome.

Ortholog Analysis

Import genomic data from non-model organisms into our Ortholog Explorer tool to easily find ortholog genes and pathways of interest.

Biodesign‍

We import genomic data into Tupac.bio Designer to allow you to quickly navigate genomic data and design constructs using the data.

Other

Considering DNA sequencing or using genomic data for your research? Get in touch to discuss your research objectives.

ADVANTAGES OF NANOPORE DNA SEQUENCING

De-novo genome sequencing

Assembles highly repetitive genomes when short-read data is not sufficient. This allows for the assembly of more complete genomes with fewer contigs.

Whole genome sequencing

Nanopore sequencing processes the entire length of DNA fragment into the pore which provides a more complete view of genetic variants.

Detection of epigenetic modifications

DNA chemical modification regulates genomic function. Epigenetic modifications can be detected by Nanopore sequencing.

Phasing of variants‍

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.