 
    Genome Sequencing
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             Discover More Discover MoreWhole Exome Sequencing is the analysis of the exonic regions of the entire DNA. 
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             Discover More Discover MoreWhole Genome Sequencing is the analysis of the entire genome, including intronic and exonic regions of DNA. 
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             Discover More Discover MoreLow Pass WGS is the analysis of the entire genome with 1X, 3X or 16X coverage. 
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             Discover More Discover MoreLong reads Whole Genome Sequencing is the analysis of the entire genome, including intronic and exonic regions of DNA delivering highly accurate long reads. 
Transcriptome Sequencing
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             Discover More Discover MoreTotal RNA sequencing (RNA-Seq) detects coding and different types of noncoding RNA. 
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             Discover More Discover MoremRNA sequencing (mRNA-Seq) is directed to the coding portion of the transcriptome. 
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             Discover More Discover MoreRibosomal RNA sequencing (rRNA seq) is used to identify and compare bacteria or fungi present within a given sample. 
Flow Cell: Purchasing this service allows the dedicated, exclusive and personalized loading of all the samples in the same flow cell or lane.
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              S4 Flow CellDiscover More
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              10B Flow CellDiscover More
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              25B Flow CellDiscover More
Solid Tumor Sequencing Test (500 genes)
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             Discover More Discover MoreTSO 500 test allows to detect cancer-related genes starting from DNA and RNA extracted from formalin-fixed paraffin embedded (FFPE) tissue. 
Pre-made Libraries Sequencing
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             Discover More Discover MoreThis service includes new generation sequencing of pre-made libraries or pools to reach a customized amount of Gb as final output. 
Metagenomics
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             Discover More Discover MoreMetagenomics is the study of genetic material, deriving directly from environmental or clinical samples, through next-generation sequencing methods. 
Mitocondrial DNA
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             Discover More Discover MoreMitochondrial sequencing enables detection and analysis of mitochondrial disease-associated variants, within the genome or exome. 
 
               
                   
                   
                   
                   
                   
                   
                   
                   
                   
                   
                   
                   
                  