Available In: United Arab Emirates, Saudi Arabia, Qatar, Bahrain, Kuwait, Oman, Iraq…
Lebanon, Yemen, Egypt, Algeria, Morocco, Tunisia and Pakistan.
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ArcherDx also allows the customer to design custom next-generation sequencing (NGS) panels for RNA, DNA, or ctDNA input to meet the needs of every lab.
AMP is a powerful method for amplifying minuscule amount of nucleic acids. Combined with Next Generation sequencing, AMP allows you to detect gene rearrangements (gene fusions) without you needing to know fusion partners from small and poor quantities of nucleic acid.
Adapters ligated to molecules before amplification carry MBCs that enable unique molecule counting and powerful error correction for confident mutation calling. MBCs help sequence analysis software’s to filter out duplicate reads and PCR errors to report unique reads.
NTRK fusions with known and unknown fusion partners that are notoriously difficult to detect are critical events in cancer biology. FusionPlex® NGS research assays provide sensitive NTRK fusion detection without prior knowledge of fusion.
