Diagnose : um futuro campo de atuação em medicina.

Next Generation Sequencing (NGS) is a type of DNA sequencing technology that uses parallel sequencing of multiple small fragments of DNA. This technology has allowed for a dramatic increase in speed (and a decrease in cost) in which an individual's genome can be sequenced. Sanger sequencing is used to confirm the presence of specific mutations identified by NGS in clinical situations due to the greater accuracy of traditional sequencing methods, although this practice is being questioned. NGS may be appropriate to diagnose suspected genetic disorders when single gene sequencing is unlikely to provide a diagnosis. NGS-based gene panels are used clinically in certain hematological malignancies, and the first genetic panel tests for solid tumors. Other uses, such as the diagnosis of infections and the screening of healthy people, continue to be investigated.