Onderzoeker
Lennart Raman
- Disciplines:Structurele bio-informatica en computationele proteomics, Ontwikkeling van bio-informatica software, tools en databases, Bio-informatica van ziekten, Bio-informatica data-integratie en netwerkbiologie
Affiliaties
- Vakgroep Diagnostische Wetenschappen (Departement)
Lid
Vanaf1 okt 2018 → 26 sep 2021 - Vakgroep Medische en Forensische Pathologie (Departement)
Lid
Vanaf1 aug 2017 → 30 sep 2018
Publicaties
1 - 10 van 13
- GENType : all-in-one preimplantation genetic testing by pedigree haplotyping and copy number profiling suitable for third-party reproduction(2022)
Auteurs: Lisa De Witte, Lennart Raman, Machteld Baetens, Andries De Koker, Kelly Tilleman, Frauke Vanden Meerschaut, Annelies Dheedene
Pagina's: 1678 - 1691 - Application of an ultrasensitive NGS-based blood test for the diagnosis of early-stage lung cancer : sensitivity, a hurdle still difficult to overcome(2022)
Auteurs: Malaïka Van der Linden, Bram Van Gaever, Lennart Raman, Karim Vermaelen, Ingel Demedts, Veerle Surmont, Ulrike Himpe, Yolande Lievens, Liesbeth Ferdinande, Franceska Dedeurwaerdere, et al.
- Copy number and methylation profiling of cell-free DNA for tumor and prenatal diagnostics : a multi-cohort research effort(2021)
Auteurs: Lennart Raman
- Shallow whole-genome sequencing of plasma cell-free DNA accurately differentiates small from non-small cell lung carcinoma(2020)
Auteurs: Lennart Raman, Malaïka Van der Linden, Kim Van der Eecken, Karim Vermaelen, Ingel Demedts, Veerle Surmont, Ulrike Himpe, Franceska Dedeurwaerdere, Liesbeth Ferdinande, Yolande Lievens, et al.
- Shallow-depth sequencing of cell-free DNA for Hodgkin and diffuse large B-cell lymphoma (differential) diagnosis : a standardized approach with underappreciated potential
Auteurs: Lennart Raman, Malaïka Van der Linden, Ciel De Vriendt, Bliede Van den Broeck, Kristoff Muylle, Dries Deeren, Franceska Dedeurwaerdere, Amélie Dendooven, Katrien De Grove, Saskia Baert
Pagina's: 211 - 220 - Exploring the potential of shallow whole-genome sequencing for diagnosis and disease monitoring of lymphoma in liquid biopsyVolume: 134
Auteurs: Lennart Raman, Malaïka Van der Linden, Ciel De Vriendt, Bliede Van den Broeck, Kristoff Muylle, Dries Deeren
Aantal pagina's: 1 - The feasibility of using liquid biopsies as a complementary assay for copy number aberration profiling in routinely collected paediatric cancer patient samples
Auteurs: Ruben Van Paemel, Charlotte Vandeputte, Lennart Raman, Jolien Van Thorre, Leen Willems, Jilke De Wilde, Andries De Koker, Christine Devalck, Ales Vicha, Marek Grega, et al.
Pagina's: 12 - 23 - Shallow whole-genome sequencing : a useful, easy to apply molecular technique for CNA detection on FFPE tumor tissue : a glioma-driven study
Auteurs: Kim Van der Eecken, Malaïka Van der Linden, Lennart Raman, Franceska Dedeurwaerdere, Koen De Winne, Martin Lammens, Isabelle Rottiers, Bram Van Gaever, Caroline Van den Broecke
Pagina's: 677 - 686 - Detection of copy number alterations by shallow whole-genome sequencing of formalin-fixed, paraffin-embedded tumor tissue
Auteurs: Lennart Raman, Ansel Vander Trappen, Annelies Dheedene, Tom Sante
Pagina's: 974 - 981 - Myxoid pleomorphic liposarcoma : a clinicopathologic, immunohistochemical, molecular genetic and epigenetic study of 12 cases, suggesting a possible relationship with conventional pleomorphic liposarcoma
Auteurs: Andrew L. Folpe, Christian Koelsche, Thomas Mentzel, Joost M. van Gorp, Malaïka Van der Linden, Lennart Raman, Karen Fritchie, Andreas von Deimling, Uta Flucke
Pagina's: 2043 - 2049