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W ostatnich latach odchodzi się od stosowania zautomatyzowanego sekwencjonowania metodą Sangera w analizach genomu. Nowsze metody sekwencjonowania, określane jako Sekwencjonowanie Następnej Generacji (NGS), opierają się na połączeniu: przygotowania i sekwencjonowania szablonu, przetworzenia obrazu oraz metod wyrównania i montażu genomu. STAB VIDA, dzięki swym platformom NGS, oferuje możliwość produkcji ogromnych ilości danych - w niektórych przypadkach ponad miliard krótkich odczytów na jedno uruchomienie instrumentu. W naszej firmie mikromacierze do badań ekspresji genów są zastąpione metodami seq-based, które mogą zidentyfikować i określić ilościowo rzadkie transkrypty bez uprzedniej znajomości danego genu i mogą dostarczyć informacji dotyczących alternatywnego splicingu i zmienności sekwencji genu. Możliwość sekwencjonowania całego genomu wielu spokrewnionych organizmów, pozwoliła na przeprowadzenie porównawczych badań ewolucyjnych na dużą skalę, które były niewyobrażalne jeszcze kilka lat temu. Oferujemy resequencing ludzkich genomów, celem zwiększenia zrozumienia, jak różnice genetyczne wpływają na stan zdrowia. Różnorodność funkcji NGS zwiększa prawdopodobieństwo  współistnienia platform na rynku.

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