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Nicolas Dierckxsens
Nicolas Dierckxsens
在 oist.jp 的电子邮件经过验证 - 首页
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NOVOPlasty: de novo assembly of organelle genomes from whole genome data
N Dierckxsens, P Mardulyn, G Smits
Nucleic acids research 45 (4), e18-e18, 2017
28112017
COLOMBOS v3. 0: leveraging gene expression compendia for cross-species analyses
M Moretto, P Sonego, N Dierckxsens, M Brilli, L Bianco, ...
Nucleic acids research 44 (D1), D620-D623, 2016
632016
Unraveling heteroplasmy patterns with NOVOPlasty
N Dierckxsens, P Mardulyn, G Smits
NAR Genomics and Bioinformatics 2 (1), lqz011, 2020
512020
A benchmark of structural variation detection by long reads through a realistic simulated model
N Dierckxsens, T Li, JR Vermeesch, Z Xie
Genome biology 22, 1-16, 2021
352021
Multichromosomal Mitochondrial Genome of Paphiopedilum micranthum: Compact and Fragmented Genome, and Rampant Intracellular Gene Transfer
JX Yang, N Dierckxsens, MZ Bai, YY Guo
International Journal of Molecular Sciences 24 (4), 3976, 2023
172023
Parental genomes segregate into distinct blastomeres during multipolar zygotic divisions leading to mixoploid and chimeric blastocysts
T De Coster, H Masset, O Tšuiko, M Catteeuw, Y Zhao, N Dierckxsens, ...
Genome Biology 23 (1), 201, 2022
122022
22q11. 2 low copy repeats expanded in the human lineage
L Vervoort, N Dierckxsens, Z Pereboom, O Capozzi, M Rocchi, TH Shaikh, ...
Frontiers in genetics 12, 706641, 2021
112021
Primary mediastinal large B‐cell lymphoma is characterized by large‐scale copy‐neutral loss of heterozygosity
S Tuveri, K Debackere, L Marcelis, N Dierckxsens, J Demeulemeester, ...
Genes, Chromosomes and Cancer 61 (10), 603-615, 2022
52022
Tracing Homopolymers in Oikopleura dioica's mitogenome
N Dierckxsens, K Watanabe, Y Tan, A Masunaga, MJ Mansfield, J Miao, ...
bioRxiv, 2024.05. 16.594446, 2024
12024
Parental genomes segregate into different blastomeres during multipolar zygotic divisions leading to mixoploid and chimeric blastocysts
T De Coster, H Masset, O Tšuiko, M Catteeuw, N Dierckxsens, S Debrock, ...
bioRxiv, 2021.11. 05.467317, 2021
12021
Human-specific expansion of 22q11. 2 low copy repeats
L Vervoort, N Dierckxsens, Z Pereboom, O Capozzi, M Rocchi, TH Shaikh, ...
bioRxiv, 2020.11. 04.367920, 2020
12020
The complete mitogenome of an unidentified Oikopleura species
JN Wibisana, C Plessy, N Dierckxsens, A Masunaga, J Miao, ...
bioRxiv, 2024.07. 04.602139, 2024
2024
Multiple paralogues and recombination mechanisms drive the high incidence of 22q11. 2 Deletion Syndrome
L Vervoort, N Dierckxsens, M Sousa Santos, S Meynants, E Souche, ...
bioRxiv, 2024.03. 14.585046, 2024
2024
22q11. 2 rearrangements caused by NAHR and PATRR-mediated pathways
L Vervoort, N Dierckxsens, B Zhou, R Cools, T Heung, G Peeters, ...
European Journal Of Human Genetics 31, 59-59, 2023
2023
Primary mediastinal large B-cell lymphoma is hallmarked by large-scale copy-neutral loss of heterozygosity
S Tuveri, K Debackere, L Marcelis, N Dierckxsens, J Demeulemeester, ...
European Journal Of Human Genetics 31, 525-525, 2023
2023
FiberFISH mapping of 22q11. 2 rearrangements shows locus heterogeneity
R Cools, L Vervoort, N Dierckxsens, T Heung, G Peeters, A Swillen, ...
Joint Meeting BeSHG/NVHG, Location: BMCC, Brugge, 2022
2022
22q11. 2 inversion in a mosaic 22q11. 2 deletion patient provides insights in LCR22-mediated rearrangements
L Vervoort, G Peeters, N Dierckxsens, L Dehaspe, L Vancoillie, ...
European Journal Of Human Genetics 30 (SUPPL 1), 82-82, 2021
2021
TARGETED ORGANELLE GENOME ASSEMBLY AND HETEROPLASMY DETECTION
N Dierckxsens
Université Libre de Bruxelles, 2018
2018
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