High-throughput sequencing

Four your high-throughput sequencing needs, we offer a range of Targeted Sequencing applications encompassing various gene panels, as well as Whole Exome Sequencing (WES), for the detection of both somatic and germline variation in DNA and RNA extracted from blood, FFPE, bone marrow, fresh tissue, cell-free DNA in plasma, and other sample materials.

In addition to services combining library preparation and sequencing, we also offer access to our sequencing instruments for researchers who produce their own sequencing libraries.

Appplication

Technology

Method

Material

Source

Whole Exome Sequencing

Illumina

Twist Human Comprehensive Exome

DNA

Blood

Whole Exome Sequencing

Illumina

Agilent SureSelect XT All Exon v7

DNA

Blood, FFPE

Targeted  Exome Sequencing

Illumina

TruSight Oncology 500 DNA (SNV, Indels, CNVs, MSI, TMB)

DNA

Blood, FFPE

Targeted  Exome Sequencing

Illumina

TruSight Oncology 500 RNA (gene fusions)

RNA

Blood, FFPE

Targeted  Exome Sequencing

Illumina

TruSight RNA Fusion Panel

RNA

Blood, FFPE

Targeted  Exome Sequencing

Iontorrent

AmpliSeq Cancer Hotspot Panel

DNA

Blood, FFPE

Targeted  Exome Sequencing

Iontorrent

Gene panels for mutation detection in hematologic malignancies

DNA

Blood, bone marrow

Targeted  Exome Sequencing

Iontorrent

Gene panels for rearrangement detection in hematologic malignancies

RNA

Blood, bone marrow

Liquid Biopsy

Illumina

Roche AVENIO ctDNA Panels

cell-free DNA

Plasma

Targeted  Exome Sequencing

Illumina

Oncogenetics panel

DNA

Blood, fresh tissue

Mitochondrial Sequencing

Illumina

Mitochondrial genome

DNA

Blood, fresh tissue

Given the diversity of sequencing options, we offer support in the planning of your experiments and the selection of the optimal method for your study. Please contact us via E-Mail to schedule a meeting or for cost estimates.