Ghent University Academic Bibliography

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Short tandem repeat analysis after whole genome amplification of single B-lymphoblastoid cells

Lieselot Deleye (UGent) , Ann-Sophie Vander Plaetsen (UGent) , Jana Weymaere (UGent) , Dieter Deforce (UGent) and Filip Van Nieuwerburgh (UGent)

(2018) SCIENTIFIC REPORTS. 8.
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Massively parallel sequencing of micro-manipulated cells targeting a comprehensive panel of disease-causing genes : a comparative evaluation of upstream whole-genome amplification methods

Lieselot Deleye (UGent) , Yannick Gansemans (UGent) , Dieter De Coninck (UGent) , Filip Van Nieuwerburgh (UGent) and Dieter Deforce (UGent)

(2018) PLOS ONE. 13(4).
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STR profiling and Copy Number Variation analysis on single, preserved cells using current Whole Genome Amplification methods

Ann-Sophie Vander Plaetsen (UGent) , Lieselot Deleye (UGent) , Senne Cornelis (UGent) , Laurentijn Tilleman (UGent) , Filip Van Nieuwerburgh (UGent) and Dieter Deforce (UGent)

(2017) SCIENTIFIC REPORTS. 7.
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Performance of four modern whole genome amplification methods for copy number variant detection in single cells

Lieselot Deleye (UGent) , Laurentijn Tilleman (UGent) , Ann-Sophie Vander Plaetsen (UGent) , Senne Cornelis (UGent) , Dieter Deforce (UGent) and Filip Van Nieuwerburgh (UGent)

(2017) SCIENTIFIC REPORTS. 7.
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Forensic SNP genotyping using nanopore MinION sequencing

Senne Cornelis (UGent) , Yannick Gansemans (UGent) , Lieselot Deleye (UGent) , Dieter Deforce (UGent) and Filip Van Nieuwerburgh (UGent)

(2017) SCIENTIFIC REPORTS. 7.
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Preimplantation genetic diagnosis (PGD) for translocation carriers using whole genome screening by microarray analysis at the blastocyst stage

CHRISTODOULOS CHRISTODOULOU (UGent) , Annelies Dheedene (UGent) , Ilse De Croo (UGent) , Björn Heindryckx (UGent) , Lieselot Deleye (UGent) , Filip Van Nieuwerburgh (UGent) , Dieter Deforce (UGent) , Petra De Sutter (UGent) , Björn Menten (UGent) and Etienne Van den Abbeel (UGent)

(2016) HUMAN REPRODUCTION. In Human Reproduction 31(supplement 1). p.386-387
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Performance of a TthPrimPol-based whole genome amplification kit for copy number alteration detection using massively parallel sequencing

Lieselot Deleye (UGent) , Dieter De Coninck (UGent) , Annelies Dheedene (UGent) , Petra De Sutter (UGent) , Björn Menten (UGent) , Dieter Deforce (UGent) and Filip Van Nieuwerburgh (UGent)

(2016) SCIENTIFIC REPORTS. 6.
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Shallow whole genome sequencing is well suited for the detection of chromosomal aberrations in human blastocysts

Lieselot Deleye (UGent) , Annelies Dheedene (UGent) , Dieter De Coninck (UGent) , Tom Sante (UGent) , CHRISTODOULOS CHRISTODOULOU (UGent) , Björn Heindryckx (UGent) , Etienne Van den Abbeel (UGent) , Petra De Sutter (UGent) , Dieter Deforce (UGent) , Björn Menten (UGent) , et al.

(2015) FERTILITY AND STERILITY. 104(5). p.1276-1285
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Whole genome amplification with SurePlex results in better copy number alteration detection using sequencing data compared to the MALBAC method

Lieselot Deleye (UGent) , Dieter De Coninck (UGent) , CHRISTODOULOS CHRISTODOULOU (UGent) , Tom Sante (UGent) , Annelies Dheedene (UGent) , Björn Heindryckx (UGent) , Etienne Van den Abbeel (UGent) , Petra De Sutter (UGent) , Björn Menten (UGent) , Dieter Deforce (UGent) , et al.

(2015) SCIENTIFIC REPORTS. 5.

Academic Bibliography

Short tandem repeat analysis after whole genome amplification of single B-lymphoblastoid cells

Massively parallel sequencing of micro-manipulated cells targeting a comprehensive panel of disease-causing genes : a comparative evaluation of upstream whole-genome amplification methods

STR profiling and Copy Number Variation analysis on single, preserved cells using current Whole Genome Amplification methods

Performance of four modern whole genome amplification methods for copy number variant detection in single cells

Forensic SNP genotyping using nanopore MinION sequencing

Preimplantation genetic diagnosis (PGD) for translocation carriers using whole genome screening by microarray analysis at the blastocyst stage

Performance of a TthPrimPol-based whole genome amplification kit for copy number alteration detection using massively parallel sequencing

Shallow whole genome sequencing is well suited for the detection of chromosomal aberrations in human blastocysts

Whole genome amplification with SurePlex results in better copy number alteration detection using sequencing data compared to the MALBAC method

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