ORION

Comprehensive Backbone:

More than Just Exome!

whole-exome

Whole Exome

cnv-calling

CNV Calling *

mitochondrial-genome

Mitochondrial Genome

Coverage:

Inclusive Of

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>19,000 genes * *

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100X Mean Depth

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>95% Coverage @20X

Customized Gene Curation:

Towards Evidence Based Medicine

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Phenotype Specific

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Regularly Updated Gene Lists

Enhanced Variant Calling:

Enriching Analysis!

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Customized Pipeline

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Extensively Validated

Expert Variant Annotation:

Adding Relevance to Reporting!

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Gene-Disease Association

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Variant-Disease Association

Best-in-Class Reports:

Peer reviwed by:

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Bionformatician

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PhD Scientist

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Genetic Counselor

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Clinical Geneticist

Indications:

Available as:

Acceptable Samples:

TAT: 28 Working Days
Rapid TAT15 Working days
Express TAT 7 Working days
  • *CNV calling is validated for multi-exon CNV (>/= 3)
  • Confirmation of detected CNV’s by an alternate method is recommended
  • ** Sequencing included coding region with +/-10 bp are included

PRENATAL NGS

Indications:

Family history of a known genetic disorder

Antenatal detection of fetal malformations

Pre-requisite:

Maternal Cell Contamination testing (MCC) is MANDATORY

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Accreditations

The above accreditations have been granted to NEUBERG SUPRATECH REFERENCE LABORATORIES PRIVATE LIMITED (NSRL). The Neuberg Center for Genomic Medicine (NCGM) is affiliated to NSRL.