Lennart Raman

Gent, VLG 9000, Belgium

Last Updated: 09/26/2026

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Found 10 publications

Application of an Ultrasensitive NGS-Based Blood Test for the Diagnosis of Early-Stage Lung Cancer: Sensitivity, a Hurdle Still Difficult to Overcome.

Application of an Ultrasensitive NGS-Based Blood Test for the Diagnosis of Early-Stage Lung Cancer: Sensitivity, a Hurdle Still Difficult to Overcome.

Journal: Cancers

Published: March 17, 2022

GENType: all-in-one preimplantation genetic testing by pedigree haplotyping and copy number profiling suitable for third-party reproduction.

GENType: all-in-one preimplantation genetic testing by pedigree haplotyping and copy number profiling suitable for third-party reproduction.

Journal: Human reproduction (Oxford, England)

Published: November 22, 2021

Shallow whole-genome sequencing: a useful, easy to apply molecular technique for CNA detection on FFPE tumor tissue-a glioma-driven study.

Shallow whole-genome sequencing: a useful, easy to apply molecular technique for CNA detection on FFPE tumor tissue-a glioma-driven study.

Journal: Virchows Archiv : an international journal of pathology

Published: August 16, 2021

The feasibility of using liquid biopsies as a complementary assay for copy number aberration profiling in routinely collected paediatric cancer patient samples.

The feasibility of using liquid biopsies as a complementary assay for copy number aberration profiling in routinely collected paediatric cancer patient samples.

Journal: European journal of cancer (Oxford, England : 1990)

Published: May 12, 2021

Myxoid pleomorphic liposarcoma-a clinicopathologic, immunohistochemical, molecular genetic and epigenetic study of 12 cases, suggesting a possible relationship with conventional pleomorphic liposarcoma.

Myxoid pleomorphic liposarcoma-a clinicopathologic, immunohistochemical, molecular genetic and epigenetic study of 12 cases, suggesting a possible relationship with conventional pleomorphic liposarcoma.

Journal: Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc

Published: February 15, 2021

Shallow-depth sequencing of cell-free DNA for Hodgkin and diffuse large B-cell lymphoma (differential) diagnosis: a standardized approach with underappreciated potential.

Shallow-depth sequencing of cell-free DNA for Hodgkin and diffuse large B-cell lymphoma (differential) diagnosis: a standardized approach with underappreciated potential.

Journal: Haematologica

Published: August 03, 2020

Detection of Copy Number Alterations by Shallow Whole-Genome Sequencing of Formalin-Fixed, Paraffin-Embedded Tumor Tissue.

Detection of Copy Number Alterations by Shallow Whole-Genome Sequencing of Formalin-Fixed, Paraffin-Embedded Tumor Tissue.

Journal: Archives of pathology & laboratory medicine

Published: December 18, 2019

Shallow whole-genome sequencing of plasma cell-free DNA accurately differentiates small from non-small cell lung carcinoma.

Shallow whole-genome sequencing of plasma cell-free DNA accurately differentiates small from non-small cell lung carcinoma.

Journal: Genome medicine

Published: November 06, 2019

PREFACE: In silico pipeline for accurate cell-free fetal DNA fraction prediction.

PREFACE: In silico pipeline for accurate cell-free fetal DNA fraction prediction.

Journal: Prenatal diagnosis

Published: February 11, 2019

WisecondorX: improved copy number detection for routine shallow whole-genome sequencing.

WisecondorX: improved copy number detection for routine shallow whole-genome sequencing.

Journal: Nucleic acids research

Published: September 11, 2018

Showing 1-10 of 10

Last Updated: 09/26/2026