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.
|Whole Exome Sequencing||Illumina||Agilent SureSelect All Exon v7||DNA||Blood, FFPE|
|Liquid Biopsy||Illumina||Roche AVENIO ctDNA Panels||cell-free DNA||Plasma|
|Targeted Gene Sequencing||Illumina||Roche AVENIO Tissue Panels||DNA||FFPE|
|Targeted Gene Sequencing||Ion Torrent||Oncomine Focus, Oncomine Comprehensive||DNA||Blood, FFPE|
|Mutational Burden||Ion Torrent||Oncomine Tumor Mutation Load Assay||DNA||Blood, FFPE|
|Targeted Gene Sequencing||Ion Torrent||Gene panels for mutation detection in hematologic malignancies||DNA||Blood, bone marrow|
|Targeted Gene Sequencing||Ion Torrent||Gene panels for rearrangement detection in hematologic malignancies||RNA||Blood, bone marrow|
|Targeted Gene Sequencing||Ion Torrent||Gene panels for hereditary hemopathies||DNA||Blood|
|Clinical Exome||Illumina||TruSight One Expanded||DNA||Blood, fresh tissue|
|Targeted Gene Sequencing||Illumina||Gene panels for inherited disorders||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.