Grand Projet
Dutreux F et al.
De novo assembly and annotation of three Leptosphaeria genomes using Oxford Nanopore MinION sequencing
Scientific Data 2018 5
doi: DOI:10.1038/sdata.2018.235
Girard E et al.
Familial breast cancer and DNA repair genes: Insights into known and novel susceptibility genes from the GENESIS study, and implications for multigene panel testing
International Journal of Cancer 2018 144(8)
doi: 10.1002/ijc.31921
Khan W et al.
MACARON: a python framework to identify and re-annotate multi-base affected codons in whole genome/exome sequence data
Bioinformatics 2018 34(19)
doi: 10.1093/bioinformatics/bty382
Lornage X et al.
Novel SPEG Mutations in Congenital Myopathy without Centralized Nuclei
Journal of Neuromuscular Diseases 2018 5(2)
doi: 10.3233/JND-170265
Chicard M et al.
Whole-Exome Sequencing of Cell-Free DNA Reveals Temporo-spatial Heterogeneity and Identifies Treatment-Resistant Clones in Neuroblastoma
Clinical Cancer Research 2017 24(4)
doi: 10.1158/1078-0432.CCR-17-1586
Angela Bellini et al.
Study of chromatin remodeling genes implicates SMARCA4 as a putative player in oncogenesis in neuroblastoma
International Journal of Cancer 2019, vol. 145, issue 10
doi: 10.1002/ijc.32361
Emmanuelle Boscher et al.
Copy Number Variants in miR-138 as a Potential Risk Factor for Early-Onset Alzheimer’s Disease
Journal of Alzheimer's Disease 2019, vol. 68, issue 3
doi: 10.3233/jad-180940
Battle Karimi et al.
Biogeography of Soil Bacterial Networks along a Gradient of Cropping Intensity
Scientific Reports 2019, vol. 9, issue 1
doi: 10.1038/s41598-019-40422-y
Xavière Lornage et al.
ACTN2 mutations cause “Multiple structured Core Disease” (MsCD)
Acta Neuropathologica 2019, vol. 137, issue 3
doi: 10.1007/s00401-019-01963-8
Julie Ferreira de Carvalho et al.
Cytonuclear interactions remain stable during allopolyploid evolution despite repeated whole‐genome duplications in Brassica
The Plant Journal 2019, vol. 98, issue 3
doi: 10.1111/tpj.14228