Oncology Diagnostic Panel - NGS

Oncology Panels

Oncology NGS panels cater in the form of a range of cancer diagnostic NGS solutions in the oncology segment. Next generation sequencing (NGS) provides an effective solution to gather the clinically actionable genomic information on various types of cancers that in turn can be translated into suitable prognostic and treatment decisions.

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Available Kits

Oncology Diagnostic Panel - NGS
BRCA1/2 Panel
BRCA1/2 Panel enables diagnosis of germline and somatic cancer in the whole CDS (+/-40bp) and promoter regions of BRCA1 and

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BRCA2 genes with high specificity. Panel is designed to target all the major mutation types like, SNV, Indel and CNV in the Whole Exon regions of BRCA1, 2 genes (RefSeq) and validated to yield 100% coverage. Panel is compatible with a variety of sample types (Blood and FFPE) with ≥ 50 ng fragmented DNA.
Oncology Diagnostic Panel - NGS
Common Hereditary Cancer NGS Panel
Common Hereditary Cancer NGS Panel is designed to detect SNV,

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Indel and CNV mutations in 61 genes associated with common hereditary cancers.
Oncology Diagnostic Panel - NGS
Lymphoma NGS Panel
Lymphoma is a cancerous condition in the lymphatic system that includes lymph nodes, thymus gland, spleen and bone marrow.

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Lymphoma NGS Panel is an NGS assay designed to diagnose 75 genes associated with Lymphoma. This panel enables detection of all three major mutation types, SNV, indel and CNV in the 75 genes.
Oncology Diagnostic Panel - NGS
Lymphoid Leukemia NGS Panel
Lymphoid Leukemia is a cancerous condition of blood and bone marrow in which bone marrow produces an abnormally high number of lymphocytes.

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This panel supports the diagnosis of 75 genes associated with Lymphoid Leukemia. This panel enables detection of all three major mutation types, SNV, indel and CNV in the 75 genes.
Oncology Diagnostic Panel - NGS
Myeloid Leukemia NGS Panel
Myeloid Leukemia refers to a cancerous condition of bone marrow which affacts white blood cells other than lymphocytes,

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Red blood cells and platelets. This panel supports the diagnosis of 49 genes related to Myloid Leukemia. This panel enables detection of all three major mutation types, SNV, indel and CNV in the 49 genes.
Oncology Diagnostic Panel - NGS
OncoCheck Panel
OncoCheck Panel analyzes 31 oncogenes associated with inherited cancer. These were precisely selected from contract research organizations

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and numerous research studies. The panel is integrated with a robust bioinformatics system for the analysis of large deletions. The panel also provides information for HDR grade computation aid precision. This panel screens a target size of 96 kb for 31 genes to identify SNV, Indel, CNV, and chromosomal rearrangements.
Oncology Diagnostic Panel - NGS
CancerCheck 50 Panel
CancerCheck 50 Panel is an expanded NGS assay designed to detect all types of variants in over 50 genes associated with various somatic cancers.

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This panel supports the identification of all majorly occurring mutations like SNV, Indel & CNV.
Oncology Diagnostic Panel - NGS
CancerCheck 100 Panel
CancerCheck 100 Panel is a comprehensive NGS assay designed to detect all types of variants around 100 genes associated with various somatic cancers.

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This panel supports the identification of all majorly occurring mutations like SNV, Indel, CNV, and chromosomal rearrangements as well as tumor immunotherapy markers like MSI and TMB.
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