Come si effettua un test genetico?
I test genetici si effettuano mediate prelievo di campioni biologici da cui viene estratto il DNA. Una volta effettuata l’estrazione si eseguono delle analisi molecolari per individuare polimorfismi associati a prodotti proteici con alterata attività.
Quanto costa l’esame per la trombofilia?
ESAMI E PREZZI
| ESAMI DIAGNOSTICI ABORTIVITA’ RICORRENTE | PREZZO |
|---|---|
| CARIOTIPO SU MATERIALE ABORTIVO | € 174,00 |
| HLA – G | € 105,00 |
| PANNELLO TROMBOFILIA 4 MUTAZIONI:FATTORE V DI LEIDEN+FATTORE II+ MTHFR C677T+MTHFR A1298C | € 120,00 |
| PANNELLO TROMBOFILIA 5 MUTAZIONI: Fattore V: di Leiden, Y1702C, H1299R, Cambridge; Fattore II. | € 135,00 |
What is NGS and how does it work?
How NGS Works The basic next-generation sequencing process involves fragmenting DNA/RNA into multiple pieces, adding adapters, sequencing the libraries, and reassembling them to form a genomic sequence. In principle, the concept is similar to capillary electrophoresis.
How to evaluate the cost of NGS sequencing?
When evaluating NGS costs, consider the sample volume for your study. In general, for analyzing only a few (< 20) targets on a few samples, traditional methods such as Sanger sequencing or qPCR can be useful. For sequencing more than 20 target regions or high sample volumes, NGS is preferable.
How did Illumina reduce the cost of Next-Generation Sequencing (NGS)?
Since the completion of the Human Genome Project, the cost of next-generation sequencing (NGS) has decreased at a dramatic rate, outpacing Moore’s Law. Through continuous innovation, Illumina has helped reduce the cost of NGS, enabling the $1000 human genome.
Why RNA sequencing with NGS?
Find out why RNA sequencing with NGS offers wide dynamic range and high sensitivity for detecting novel transcripts. Learn More How NGS Works