Academic Bibliography

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GC content of Early Metazoan genes and its impact on gene expression levels in mammalian cell lines

Ismail Sahin Gül, Jens Staal (UGent), Paco Hulpiau (UGent), Evi De Keuckelaere (UGent), Kai Kamm, Tom Deroo, Ellen Sanders (UGent), Katrien Staes (UGent), Yasmine Driege (UGent), Yvan Saeys (UGent), et al.

(2018) GENOME BIOLOGY AND EVOLUTION. 10(3). p.909-917
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Identification of long non-coding RNAs involved in neuronal development and intellectual disability

Eva D'haene (UGent), Eva Jacobs (UGent), Pieter-Jan Volders (UGent), Tim De Meyer (UGent), Björn Menten (UGent) and Sarah Vergult (UGent)

(2016) SCIENTIFIC REPORTS. 6.
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Trisomy 21 alters DNA methylation in parent-of-origin-dependent and independent manners

Antônio Francisco Alves da Silva, Filipe Brum Machado, Érika Cristina Pavarino, Joice Matos Biselli-Périco, Bruna Lancia Zampieri, Ronaldo da Silva Francisco Junior, Pedro Thyago Mozer Rodrigues, Douglas Terra Machado, Cíntia Barros Santos-Rebouças, Maria Gomes Fernandes, et al.

(2016) PLOS ONE. 11(4).
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DNA methylation landscapes of human fetal development

Roderick C Slieker, Matthias S Roost, Liesbeth van Iperen, H Eka D Suchiman, Elmar W Tobi, Françoise Carlotti, Eelco JP de Koning, P Eline Slagboom, Bastiaan T Heijmans and Susana Marina Chuva de Sousa Lopes (UGent)

(2015) PLOS GENETICS. 11(10).
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Profiling of conserved non-coding elements upstream of SHOX and functional characterisation of the SHOX cis-regulatory landscape

Hannah Verdin (UGent), Ana Fernández-Miñán, Sara Benito-Sanz, Sandra Janssens, Bert Callewaert (UGent), Kathleen De Waele, Jean De Schepper (UGent), Inge François, Björn Menten (UGent), Karen E Heath, et al.

(2015) SCIENTIFIC REPORTS. 5.
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We are all individuals...: bioinformatics in the personalized medicine era

Leander Van Neste and Wim Van Criekinge (UGent)

(2015) CELLULAR ONCOLOGY. 38(1). p.29-37
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SNP-guided identification of monoallelic DNA-methylation events from enrichment-based sequencing data

Sandra Steyaert, Wim Van Criekinge (UGent), Ayla De Paepe, Simon Denil, Klaas Mensaert, Katrien Vandepitte, Wim Vanden Berghe (UGent), Geert Trooskens (UGent) and Tim De Meyer (UGent)

(2014) NUCLEIC ACIDS RESEARCH. 42(20).
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Quantification of integrated HIV DNA by repetitive-sampling Alu-HIV PCR on the basis of Poisson statistics

Ward De Spiegelaere (UGent), Eva Malatinková (UGent), Lindsay Lynch, Filip Van Nieuwerburgh (UGent), Peter Messiaen (UGent), Una O'Doherty and Linos Vandekerckhove (UGent)

(2014) CLINICAL CHEMISTRY. 60(6). p.886-895
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Mate pair sequencing for the detection of chromosomal aberrations in patients with intellectual disability and congenital malformations

Sarah Vergult (UGent), Ellen Van Binsbergen, Tom Sante, Silke Nowak, Olivier Vanakker (UGent), Kathleen Claes (UGent), Bruce Poppe (UGent), Nathalie Van der Aa, Markus J van Roosmalen, Karen Duran, et al.

(2014) EUROPEAN JOURNAL OF HUMAN GENETICS. 22(5). p.652-659
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Next-generation technologies and data analytical approaches for epigenomics

Klaas Mensaert, Simon Denil, Geert Trooskens (UGent), Wim Van Criekinge (UGent), Olivier Thas (UGent) and Tim De Meyer (UGent)

(2014) ENVIRONMENTAL AND MOLECULAR MUTAGENESIS. 55(3). p.155-170

Academic Bibliography

Biblio has been updated

GC content of Early Metazoan genes and its impact on gene expression levels in mammalian cell lines

Identification of long non-coding RNAs involved in neuronal development and intellectual disability

Trisomy 21 alters DNA methylation in parent-of-origin-dependent and independent manners

DNA methylation landscapes of human fetal development

Profiling of conserved non-coding elements upstream of SHOX and functional characterisation of the SHOX cis-regulatory landscape

We are all individuals...: bioinformatics in the personalized medicine era

SNP-guided identification of monoallelic DNA-methylation events from enrichment-based sequencing data

Quantification of integrated HIV DNA by repetitive-sampling Alu-HIV PCR on the basis of Poisson statistics

Mate pair sequencing for the detection of chromosomal aberrations in patients with intellectual disability and congenital malformations

Next-generation technologies and data analytical approaches for epigenomics

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