SEQARRAY is a powerful and user-friendly application for the quick analysis of Microarray data. SEQARRAY is made for the data analysis of the Infinium GSA® (Illumina). In this array, the genotyping of a patient is easily and quickly performed on the basis of roughly 750.000 variant including insertions, deletions and CNVs. Microarrays have diverse fields of applications such as the investigation of validated polymorphisms or the analysis of mutations and for pre-screening in certain suspected diagnoses.
SEQARRAY is integrated in the SEQUENCE PILOT product family and the comparison is possible with available NGS, Sanger and MLPA results (SEQNEXT, SEQPATIENT, MLPA®).
Comfortable workflow for a quick analysis of Microarray data
Easy and fast genotyping of a patient based on roughly 750.000 variants including insertions, deletions and CNVs
Combined perfectly with Infinium® GSA (Illumina)
High sample troughput with minimum temporal and financial effort
Integrated in the SEQUENCE Pilot product family
Simple comparison with already available NGS, Sanger and MLPA results (SEQNEXT, SEQPATIENT, MLPA®)
Standardized import of GenomeStudio 2.0 data
Selection of genes of interest via gene lists
Clear and patient-oriented display of all variants including CNVs
Additional information like HGVS, QC-values, rs-number