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SEQARRAY FOR THE ANALYSIS OF YOUR
MICROARRAY DATA

NO CLOUD - STAY IN CONTROL OF YOUR DATA

SEQARRAY

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®).

We have a new publication for SeqArray: Array genotyping as diagnostic approach in medical genetics, DOI: 10.1002/mgg3.2016

  • HIGHLIGHTS

    • 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
    • Diverse possibilities for variant filtering
    • CNV visualisation based on illumina CNVPartition Algorithms (version 3.1.4)
    • Array genotyping as diagnostic approach in medical genetics, DOI: 10.1002/mgg3.2016

     
  • 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
  • Diverse possibilities for variant filtering
  • CNV visualisation based on illumina CNVPartition Algorithms (version 3.1.4)
  • Array genotyping as diagnostic approach in medical genetics, DOI: 10.1002/mgg3.2016