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Lymphoid Neoplasm, NGS, Varies

Order Code
1425022
CPT
81455
Test Details
Synonyms

ALL; CLL; Diffuse Large B-Cell Lymphoma; Follicular Lymphoma; Hairy Cell Leukemia; Splenic Marginal Zone Lymphoma; T-cell Lymphoma

TAT

14 days

Methodology

Next Generation Sequencing (NGS)

Performing Location

Accredited NRL Laboratory

Testing Frequency

Contact Technical Support

Test Overview

Lymphoid Neoplasm NGS Testing, a comprehensive DNA-based next-generation sequencing assay covering 112 genes, designed to support precision diagnostics in lymphoid malignancies. This assay provides integrated molecular profiling aligned with the WHO Classification of Haematolymphoid Tumours (5th Edition) and NCCN clinical guidelines, supporting diagnostic classification, prognostic stratification, and therapeutic decision-making across a broad spectrum of lymphoid neoplasms, including:
• Acute Lymphoblastic Leukemia (ALL)
• Chronic Lymphocytic Leukemia / Small Lymphocytic Lymphoma (CLL/SLL)
• Diffuse Large B-Cell Lymphoma (DLBCL)
• Follicular Lymphoma
• Hairy Cell Leukemia
• Splenic Marginal Zone Lymphoma
• T-Cell Lymphomas

Specimen Type

Bone Marrow (BM) Aspirate; Peripheral Blood (PB); extracted gDNA; Bone Marrow Aspirate Smears (preferably unstained); Fresh or FFPE tissue

Volume

BM, 3mL; PB, 5mL; BM Aspirate Smears, 5 slides; gDNA, 200ng

Specimen Container

EDTA for BM and PB; Fresh tissue in saline; FFPE blocks

Patient Preparation

No special preparation is required for this test. You may eat, drink, and take your medications as normal, unless instructed otherwise by your healthcare provider.

Collection

This test does not require any special collection or pre-analytical handling. Follow routine specimen collection protocols.

Specimen Stability
Temperature Period
FFPE blocks at room temperature all other samples refrigerated
Order Code
1425022
CPT
81455
Test Details
Synonyms

ALL; CLL; Diffuse Large B-Cell Lymphoma; Follicular Lymphoma; Hairy Cell Leukemia; Splenic Marginal Zone Lymphoma; T-cell Lymphoma

TAT

14 days

Methodology

Next Generation Sequencing (NGS)

Performing Location

Accredited NRL Laboratory

Testing Frequency

Contact Technical Support

Test Overview

Lymphoid Neoplasm NGS Testing, a comprehensive DNA-based next-generation sequencing assay covering 112 genes, designed to support precision diagnostics in lymphoid malignancies. This assay provides integrated molecular profiling aligned with the WHO Classification of Haematolymphoid Tumours (5th Edition) and NCCN clinical guidelines, supporting diagnostic classification, prognostic stratification, and therapeutic decision-making across a broad spectrum of lymphoid neoplasms, including:
• Acute Lymphoblastic Leukemia (ALL)
• Chronic Lymphocytic Leukemia / Small Lymphocytic Lymphoma (CLL/SLL)
• Diffuse Large B-Cell Lymphoma (DLBCL)
• Follicular Lymphoma
• Hairy Cell Leukemia
• Splenic Marginal Zone Lymphoma
• T-Cell Lymphomas

Specimen Type

Bone Marrow (BM) Aspirate; Peripheral Blood (PB); extracted gDNA; Bone Marrow Aspirate Smears (preferably unstained); Fresh or FFPE tissue

Volume

BM, 3mL; PB, 5mL; BM Aspirate Smears, 5 slides; gDNA, 200ng

Specimen Container

EDTA for BM and PB; Fresh tissue in saline; FFPE blocks

Patient Preparation

No special preparation is required for this test. You may eat, drink, and take your medications as normal, unless instructed otherwise by your healthcare provider.

Collection

This test does not require any special collection or pre-analytical handling. Follow routine specimen collection protocols.

Specimen Stability
Temperature Period
FFPE blocks at room temperature all other samples refrigerated