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Massive Parallel Sequencing
Whole Genome Sequencing
Non-Invasive Prenatal Testing (NIPT)
Human genome sequencing
Sars-Cov2 sequencing
Whole Exome Sequencing
Gene Panels
Whole Exome Sequencing
Solid and Hematological Tumors (STHT)
Hereditary Breast+Ovarian cancer - STHT
Gene fusion panel - TSO500
HLA typing via Omixon Holotype 24/7 v3
Lymfoid Malignancies - IGH, IGK and TCR
Sample Switch variant panel (SSW)
RNA sequencing
Single-cell sequencing
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DNA and RNA quantification
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Downloads
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Frequently Asked Questions
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Sample submission
How to get your samples to BRIGHTcore in a controlled fashion
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