Next-Generation Sequencing (NGS)
or massive sequencing
Next Generation Sequencing (NGS) or massive sequencing is a consolidated technology widely used by laboratories in a wide variety of areas which allows for the simultaneous sequencing of millions of DNA sequences.
What can it be used for?
NGS has various applications ranging from diagnosis and prognosis to research in the field of oncology, hereditary diseases, infectious diseases, etc., and even preimplantation genetic analyses, human identification for forensic studies or HLA typing for organ transplants, to mention but a few.
Key Aspects
Multiplexing Samples
It allows several samples to be sequenced in a single run.
Solutions for each Application
Gene panels, clinical and whole exome sequencing and whole genome sequencing.
High Sensitivity
It makes the detection of low-frequency variants possible.
Mutation Detection
Aside from the substitutions and small indels identified by Sanger, large deletions, rearrangements or CNVs can be detected
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