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Application of an Ultrasensitive NGS-Based Blood Test for the Diagnosis of Early-Stage Lung Cancer: Sensitivity, a Hurdle Still Difficult to Overcome.
Published in:
Cancers, 2022, v. 14, n. 8, p. 2031, doi. 10.3390/cancers14082031
By:
- Van der Linden, Malaïka;
- Van Gaever, Bram;
- Raman, Lennart;
- Vermaelen, Karim;
- Demedts, Ingel;
- Surmont, Veerle;
- Himpe, Ulrike;
- Lievens, Yolande;
- Ferdinande, Liesbeth;
- Dedeurwaerdere, Franceska;
- Van der Meulen, Joni;
- Claes, Kathleen;
- Menten, Björn;
- Van Dorpe, Jo
Publication type:
Article
WisecondorX: improved copy number detection for routine shallow whole-genome sequencing.
Published in:
Nucleic Acids Research, 2019, v. 47, n. 4, p. 1605, doi. 10.1093/nar/gky1263
By:
- Raman, Lennart;
- Dheedene, Annelies;
- De Smet, Matthias;
- Van Dorpe, Jo;
- Menten, Björn
Publication type:
Article
PREFACE: In silico pipeline for accurate cell-free fetal DNA fraction prediction.
Published in:
2019
By:
- Raman, Lennart;
- Baetens, Machteld;
- De Smet, Matthias;
- Dheedene, Annelies;
- Van Dorpe, Jo;
- Menten, Björn
Publication type:
journal article
Shallow whole-genome sequencing: a useful, easy to apply molecular technique for CNA detection on FFPE tumor tissue—a glioma-driven study.
Published in:
Virchows Archiv: European Journal of Pathology, 2022, v. 480, n. 3, p. 677, doi. 10.1007/s00428-022-03268-w
By:
- Van der Eecken, Kim;
- Van der Linden, Malaïka;
- Raman, Lennart;
- Creytens, David;
- Dedeurwaerdere, Franceska;
- De Winne, Koen;
- Ferdinande, Liesbeth;
- Lammens, Martin;
- Menten, Björn;
- Rottiers, Isabelle;
- Van Gaever, Bram;
- Van den Broecke, Caroline;
- Van de Vijver, Koen;
- Van Roy, Nadine;
- Verbeke, Sofie;
- Van Dorpe, Jo
Publication type:
Article
Shallow whole-genome sequencing of plasma cell-free DNA accurately differentiates small from non-small cell lung carcinoma.
Published in:
Genome Medicine, 2020, v. 12, n. 1, p. 1, doi. 10.1186/s13073-020-00735-4
By:
- Raman, Lennart;
- Van der Linden, Malaïka;
- Van der Eecken, Kim;
- Vermaelen, Karim;
- Demedts, Ingel;
- Surmont, Veerle;
- Himpe, Ulrike;
- Dedeurwaerdere, Franceska;
- Ferdinande, Liesbeth;
- Lievens, Yolande;
- Claes, Kathleen;
- Menten, Björn;
- Van Dorpe, Jo
Publication type:
Article
Detection of Copy Number Alterations by Shallow Whole-Genome Sequencing of Formalin-Fixed, Paraffin-Embedded Tumor Tissue.
Published in:
Archives of Pathology & Laboratory Medicine, 2020, v. 144, n. 8, p. 974, doi. 10.5858/arpa.2019-0010-OA
By:
- Van der Linden, Malaïka;
- Raman, Lennart;
- Vander Trappen, Ansel;
- Dheedene, Annelies;
- De Smet, Matthias;
- Sante, Tom;
- Creytens, David;
- Lievens, Yolande;
- Menten, Björn;
- Van Dorpe, Jo;
- Van Roy, Nadine
Publication type:
Article

Found: 6

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

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

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

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 of plasma cell-free DNA accurately differentiates small from non-small cell lung carcinoma.

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