Ghent University Academic Bibliography

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Using variant databases for variant prioritization and to detect erroneous genotype-phenotype associations

Bart Broeckx (UGent) , Luc Peelman (UGent) , Jimmy Saunders (UGent) , Dieter Deforce (UGent) and Lieven Clement (UGent)

(2017) BMC BIOINFORMATICS. 18.
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Toward the most ideal case-control design with related and unrelated dogs in whole-exome sequencing studies

Bart Broeckx (UGent) , Frank Coopman (UGent) , Geert Verhoeven (UGent) , Sarah De Keulenaer (UGent) , Ellen De Meester (UGent) , Valérie Bavegems (UGent) , Pascale Smets (UGent) , Bernadette Van Ryssen (UGent) , Filip Van Nieuwerburgh (UGent) and Dieter Deforce (UGent)

(2016) ANIMAL GENETICS. 47(2). p.200-207
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An heuristic filtering tool to identify phenotype-associated genetic variants applied to human intellectual disability and canine coat colors

Bart Broeckx (UGent) , Frank Coopman (UGent) , Geert Verhoeven (UGent) , Tim Bosmans (UGent) , Ingrid Gielen (UGent) , Walter Dingemanse (UGent) , Jimmy Saunders (UGent) , Dieter Deforce (UGent) and Filip Van Nieuwerburgh (UGent)

(2015) BMC BIOINFORMATICS. 16.
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Identity-by-descent-guided mutation analysis and exome sequencing in consanguineous families reveals unusual clinical and molecular findings in retinal dystrophy

Frauke Coppieters (UGent) , Kristof Van Schil (UGent) , Miriam Bauwens (UGent) , Hannah Verdin (UGent) , Annelies De Jaegher (UGent) , Delfien Syx (UGent) , Tom Sante (UGent) , Steve Lefever (UGent) , Nouha Bouayed Abdelmoula, Fanny Depasse, et al.

(2014) GENETICS IN MEDICINE. 16(9). p.671-680

Academic Bibliography

Using variant databases for variant prioritization and to detect erroneous genotype-phenotype associations

Toward the most ideal case-control design with related and unrelated dogs in whole-exome sequencing studies

An heuristic filtering tool to identify phenotype-associated genetic variants applied to human intellectual disability and canine coat colors

Identity-by-descent-guided mutation analysis and exome sequencing in consanguineous families reveals unusual clinical and molecular findings in retinal dystrophy

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