Morgane Pierre-Jean
Morgane Pierre-Jean
Researcher at CEA, Evry, France
Verified email at - Homepage
Cited by
Cited by
New efficient algorithms for multiple change-point detection with kernels
A Celisse, G Marot, M Pierre-Jean, G Rigaill
Computational Statistics & Data Analysis 123, 200-220, 2018
Performance evaluation of DNA copy number segmentation methods
M Pierre-Jean, G Rigaill, P Neuvial
Briefings in bioinformatics 16 (4), 600-615, 2015
Clustering and variable selection evaluation of 13 unsupervised methods for multi-omics data integration
M Pierre-Jean, JF Deleuze, E Le Floch, F Mauger
Briefings in Bioinformatics, 2019
Multivariate Haplotype Analysis Of 96 Sulci Opening For 15,612 UK-Biobank Sujects
S Karkar, A Gloaguen, Y Le Guen, M Pierre-Jean, C Dandine-Roulland, ...
2019 IEEE 16th International Symposium on Biomedical Imaging (ISBI 2019 …, 2019
A study of feasibility for genome-wide haplotype association of complex traits in imaging genetics
S Karkar, Y Le Guen, C Philippe, C Dandine-Roulland, M Pierre-Jean, ...
2018 IEEE International Conference on Bioinformatics and Biomedicine (BIBM …, 2018
High heritability does not imply accurate prediction under the small additive effects hypothesis
A Frouin, C Dandine-Roulland, M Pierre-Jean, JF Deleuze, C Ambroise, ...
arXiv preprint arXiv:2007.05424, 2020
PIntMF: Une méthode de factorisation matricielle pénalisée pour l'intégration de données multi-omiques
M Pierre-Jean, F Mauger, JF Deleuze, E Le Floch
Journées de Statistique de la SFdS (volume exceptionnel), 2020
comparison of commercially available whole-genome sequencing kits for variant detection in circulating cell-free DnA
F Mauger, C Horgues, M Pierre-Jean, N Oussada, L Mesrob, JF Deleuze
Scientific reports 10 (1), 1-11, 2020
Exploring the link between additive heritability and prediction accuracy from a ridge regression perspective
A Frouin, C Dandine-Roulland, M Pierre-Jean, JF Deleuze, C Ambroise, ...
Frontiers in Genetics 11, 1294, 2020
Genome-wide haplotype association study in imaging genetics using whole-brain sulcal openings of 16,304 UK Biobank subjects.
SI Karkar, CI Dandine-Roulland, JF Mangin, Y Le Guen, C Philippe, ...
bioRxiv, 2020
Development of statistical methods for DNA copy number analysis in cancerology.
M Pierre-Jean
PSSeg: Parent-Specifc copy number segmentation
M Pierre-Jean, G Rigaill, P Neuvial
Briefings in Bioinformatics 16 (4), 600-615, 2015
Détection de ruptures à partir de méthodes à noyaux
M Pierre-Jean, G Marot, G Rigaill, A Celisse
Change-point detection with kernel methods: application to DNA copy number signals
M Pierre-Jean, G Marot, R Guillem, A Celisse
Qian Liu, ElizabethT. Cirulli, Yujun Han, Song Yao, Song Liu and Qianqian Zhu Rediscovery rate estimation for assessing the validation of significant findings in high …
A Ganna, D Lee, EI andYudi Pawitan, M Molnar, L Ilie, M Pierre-Jean, ...
Package ‘acnr’
M Pierre-Jean, P Neuvial, MM Pierre
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