Targeted resequencing

Methods to identify and study variation within specific genomic regions of interest.

HLA Typing with Nanopore Sequencing

The complexity and polymorphic nature of the 4 Mb region makes it challenging to resolve using short-read sequencing technology. Nanopore (ONT) sequencing, can provide long reads that overcome these challenges, enabling the identification of variants that could represent new biomarkers, unambiguous haplotype phasing of single-nucleotide variants (SNVs), and the potential for increased accuracy of HLA typing at a higher resolution.

Illumina 16S sequencing

Sequencing of the 16S gene to study bacterial diversity and composition in a sample.

Illumina amplicon sequencing

Sequencing of PCR amplicons to study genetic variation within small target regions.

PacBio SMRT sequencing

PacBio SMRT sequencing generates reads tens of kilobases in length enabling high quality genome assembly, structural variant analysis, amplicon resequencing, full-length transcript isoform sequencing, full-length 16S rRNA sequencing and amplification free epigenetic characterization.

RAD-sequencing

Genotyping-by-sequencing without prior genome information.