[go: up one dir, main page]

Follow
Nicolas PHILIPPE
Nicolas PHILIPPE
President & CPSO at SeqOne Genomics, PhD
Verified email at seqone.com - Homepage
Title
Cited by
Cited by
Year
MicroRNAs: new candidates for the regulation of the human cumulus–oocyte complex
S Assou, T Al-Edani, D Haouzi, N Philippe, CH Lecellier, D Piquemal, ...
Human reproduction 28 (11), 3038-3049, 2013
1532013
Long non-coding RNAs in human early embryonic development and their potential in ART
J Bouckenheimer, S Assou, S Riquier, C Hou, N Philippe, C Sansac, ...
Human reproduction update 23 (1), 19-40, 2017
1352017
CRAC: an integrated approach to the analysis of RNA-seq reads
N Philippe, M Salson, T Commes, E Rivals
Genome biology 14 (3), 1-16, 2013
912013
DE-kupl: exhaustive capture of biological variation in RNA-seq data through k-mer decomposition
J Audoux, N Philippe, R Chikhi, M Salson, M Gallopin, M Gabriel, ...
Genome biology 18 (1), 243, 2017
622017
Using reads to annotate the genome: influence of length, background distribution, and sequence errors on prediction capacity
N Philippe, A Boureux, L Bréhélin, J Tarhio, T Commes, É Rivals
Nucleic acids research 37 (15), e104-e104, 2009
302009
Combining DGE and RNA-sequencing data to identify new polyA+ non-coding transcripts in the human genome
N Philippe, E Bou Samra, A Boureux, A Mancheron, F Ruffle, Q Bai, ...
Nucleic Acids Research 42 (5), 2820-2832, 2014
232014
Querying large read collections in main memory: a versatile data structure
N Philippe, M Salson, T Lecroq, M Léonard, T Commes, E Rivals
BMC bioinformatics 12 (1), 242, 2011
212011
SimBA: A methodology and tools for evaluating the performance of RNA-Seq bioinformatic pipelines
J Audoux, M Salson, CF Grosset, S Beaumeunier, JM Holder, T Commes, ...
BMC bioinformatics 18 (1), 428, 2017
152017
Genome Alert!: A standardized procedure for genomic variant reinterpretation and automated gene–phenotype reassessment in clinical routine
K Yauy, F Lecoquierre, S Baert-Desurmont, D Trost, A Boughalem, ...
Genetics in Medicine 24 (6), 1316-1327, 2022
142022
Predominance of BRCA2 Mutation and Estrogen Receptor Positivity in Unselected Breast Cancer with BRCA1 or BRCA2 Mutation
P Pujol, K Yauy, A Coffy, N Duforet-Frebourg, S Gabteni, JP Daurès, ...
Cancers 14 (13), 3266, 2022
132022
New chimeric RNAs in acute myeloid leukemia
F Ruffle, J Audoux, A Boureux, S Beaumeunier, JB Gaillard, EB Samra, ...
F1000Research 6, ISCB Comm J-1302, 2017
112017
System for analysing genomic data comprising a plurality of application nodes and a knowledge database
N Philippe, G BUWALDA
US Patent 11,424,009, 2022
92022
Genomic analysis of adult thrombotic microangiopathies in less than 3 days: from rapid to fast genomics to treatment
N Yousfi, C Mousseaux, A Hamza, P Laville, M Mille, N Philippe, ...
Blood 144 (21), 2266-2269, 2024
82024
Clinical evaluation of a low-coverage whole-genome test for detecting homologous recombination deficiency in ovarian cancer
R Boidot, MGB Blum, MP Wissler, C Gottin, J Ruzicka, S Chevrier, ...
European Journal of Cancer 202, 113978, 2024
72024
39MO Clinical evaluation of a low-coverage whole-genome test for homologous recombination deficiency detection in ovarian cancer
R Boidot, MGB Blum, MP Wissler, C Gottin, J Ruzicka, N Duforet-Frebourg, ...
ESMO Open 8 (1), 2023
72023
Learning phenotypic patterns in genetic diseases by symptom interaction modeling
K Yauy, N Duforet-Frebourg, Q Testard, S Beaumeunier, J Audoux, ...
medRxiv, 2022.07. 29.22278181, 2022
42022
On the evaluation of the fidelity of supervised classifiers in the prediction of chimeric RNAs
S Beaumeunier, J Audoux, A Boureux, F Ruffle, T Commes, N Philippe, ...
BioData Mining 9 (1), 34, 2016
42016
The Role of Machine Learning in Finding Chimeric RNAs
S Beaumeunier, J Audoux, A Boureux, T Commes, N Philippe, R Alves
2015 26th International Workshop on Database and Expert Systems Applications …, 2015
42015
Clinical Evaluation of an AI System for Streamlined Variant Interpretation in Genetic Testing
J Ruzicka, JM Ravel, J Audoux, A Boulat, J Thévenon, K Yauy, M Dancer, ...
medRxiv, 2025.02. 04.25321641, 2025
22025
A scalable indexing solution to mine huge genomic sequence collections
E Rivals, N Philippe, M Salson, M Léonard, T Commes, T Lecroq
ERCIM News 2012 (89), 20-21, 2012
22012
The system can't perform the operation now. Try again later.
Articles 1–20