Academic Bibliography

Search 200 years of publications by Ghent University researchers.

Lies Vantomme

Faculty of Medicine and Health Sciences > Department of Biomolecular Medicine

Work address: C. Heymanslaan 10, ingang 34 (MRB)
9000 Gent
Email: Lies.Vantomme@UGent.be

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- Conference Paper
- C3
Long-read sequencing resolves cryptic structural variation in patients with syndromic intellectual disability

Griet De Clercq (UGent) , Lies Vantomme (UGent) , Bert Callewaert (UGent) , Sarah Vergult (UGent) , Annelies Dheedene (UGent) and Björn Menten (UGent)

(2022) Nanopore Community Meeting 2022, Abstracts.
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Benchmarking of long read structural variant callers using Oxford Nanopore data

Griet De Clercq (UGent) , Bram Van Gaever (UGent) , Lies Vantomme (UGent) , Annelies Dheedene (UGent) and Björn Menten (UGent)

(2022) RARE-MED Symposium 2022, Abstracts.
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- C3
Benchmarking of long-read structural variant callers using in-house generated Oxford Nanopore data

Griet De Clercq (UGent) , Bram Van Gaever (UGent) , Lies Vantomme (UGent) , Annelies Dheedene (UGent) and Björn Menten (UGent)

(2022) European Society for Human Genetics (ESHG) Conference 2022, Abstracts.
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- Conference Paper
- C3
Benchmarking of long-read structural variant callers using Oxford Nanopore data

Griet De Clercq (UGent) , Bram Van Gaever (UGent) , Lies Vantomme (UGent) , Annelies Dheedene (UGent) and Björn Menten (UGent)

(2022) Oxford Nanopore Technologies : London Calling 2022, Abstracts.
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- Conference Paper
- C3
Benchmarking of long-read structural variant callers using Oxford Nanopore data

Griet De Clercq (UGent) , Bram Van Gaever (UGent) , Lies Vantomme (UGent) , Annelies Dheedene (UGent) and Björn Menten (UGent)

(2022) Joint BeSHG / NVHG meeting 2022, Abstracts.
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- C3
- open access
A novel neurodevelopmental syndrome caused by loss-of-function of the Zinc Finger Homeobox 3 (ZFHX3) gene

Maria del Rocio Pérez Baca (UGent) , Eva Jacobs, Lies Vantomme (UGent) , Pontus LeBlanc (UGent) , Elke Bogaert (UGent) , Annelies Dheedene (UGent) , Laurenz De Cock, Bart Dermaut (UGent) , Aidin Foroutan, Jennifer Kerkhof, et al.

(2022) Joint BeSHG / NVHG meeting 2022, Abstracts.
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- Conference Paper
- C3
Mapping the 3D genome of the human retina and its role in retinal disease

Eva D'haene (UGent) , Victor Lopez Soriano (UGent) , Lies Vantomme (UGent) , Bernd Wissinger, Susanne Kohl, Sarah Vergult (UGent) and Elfride De Baere (UGent)

(2022) European Society for Human Genetics (ESHG) Conference 2022, Abstracts.
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- Conference Paper
- C3
- open access
Mapping the 3D genome of the human retina and its role in retinal disease

Eva D'haene (UGent) , Victor Lopez Soriano (UGent) , Lies Vantomme (UGent) , Bernd Wissinger, Susanne Kohl, Sarah Vergult (UGent) and Elfride De Baere (UGent)

(2022) Joint BeSHG / NVHG meeting 2022, Abstracts.
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- Conference Paper
- C3
Structural variants disrupt a critical regulatory region downstream of FOXG1

Eva D'haene (UGent) , Lies Vantomme (UGent) , Björn Menten (UGent) , Bert Callewaert (UGent) , Elfride De Baere (UGent) and Sarah Vergult (UGent)

(2021) EMBO workshop 'Enhanceropathies : Understanding enhancer function to understand human disease', Abstracts. In EMBO Workshop 'Enhanceropathies' Abstract Book
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- C3
Benchmarking of long-read structural variant callers on a recently released truth set using Oxford Nanopore data

Griet De Clercq (UGent) , Bram Van Gaever (UGent) , Lies Vantomme (UGent) , Annelies Dheedene (UGent) and Björn Menten (UGent)

(2021) Variant Effect Prediction Training Course 2021, Abstracts.

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