Hugues Richard
Hugues Richard
Robert Koch Institute (Researcher) / Sorbonne University (Ass. Prof., on leave)
Verified email at upmc.fr - Homepage
Title
Cited by
Cited by
Year
A global view of gene activity and alternative splicing by deep sequencing of the human transcriptome
M Sultan, MH Schulz, H Richard, A Magen, A Klingenhoff, M Scherf, ...
Science 321 (5891), 956-960, 2008
13622008
The genome of a songbird
WC Warren, DF Clayton, H Ellegren, AP Arnold, LDW Hillier, A Künstner, ...
Nature 464 (7289), 757-762, 2010
7422010
Assessment of transcript reconstruction methods for RNA-seq
T Steijger, JF Abril, PG Engström, F Kokocinski, M Akerman, T Alioto, ...
Nature methods 10 (12), 1177, 2013
4372013
Prediction of alternative isoforms from exon expression levels in RNA-Seq experiments
H Richard, MH Schulz, M Sultan, A Nurnberger, S Schrinner, D Balzereit, ...
Nucleic acids research 38 (10), e112-e112, 2010
1902010
Prediction of alternative isoforms from exon expression levels in RNA-Seq experiments
H Richard, MH Schulz, M Sultan, A Nurnberger, S Schrinner, D Balzereit, ...
Nucleic acids research 38 (10), e112-e112, 2010
1902010
X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes
H Hu, SA Haas, J Chelly, H Van Esch, M Raynaud, APM De Brouwer, ...
Molecular psychiatry 21 (1), 133, 2016
1532016
Erratum to: Mutation screening in 86 known X-linked mental retardation genes by droplet-based multiplex PCR and massive parallel sequencing
H Hu, K Wrogemann, V Kalscheuer, A Tzschach, H Richard, SA Haas, ...
The HUGO journal 3 (1), 83-83, 2009
67*2009
Mutation screening in 86 known X-linked mental retardation genes by droplet-based multiplex PCR and massive parallel sequencing
H Hu, K Wrogemann, V Kalscheuer, A Tzschach, H Richard, SA Haas, ...
The HUGO journal 3 (1-4), 41-49, 2009
662009
Fiona: a parallel and automatic strategy for read error correction
MH Schulz, D Weese, M Holtgrewe, V Dimitrova, S Niu, K Reinert, ...
Bioinformatics 30 (17), i356-i363, 2014
642014
Comprehensive identification and quantification of microbial transcriptomes by genome-wide unbiased methods
U Mäder, P Nicolas, H Richard, P Bessières, S Aymerich
Current Opinion in Biotechnology 22 (1), 32-41, 2011
612011
Occurrence probability of structured motifs in random sequences
S Robin, JJ Daudin, H Richard, MF Sagot, S Schbath
Journal of Computational Biology 9 (6), 761-773, 2002
582002
The diversity of small non-coding RNAs in the diatom Phaeodactylum tricornutum
A Rogato, H Richard, A Sarazin, B Voss, SC Navarro, R Champeimont, ...
BMC Genomics 15 (1), 698, 2014
252014
PureCLIP: capturing target-specific protein–RNA interaction footprints from single-nucleotide CLIP-seq data
S Krakau, H Richard, A Marsico
Genome biology 18 (1), 240, 2017
172017
Ulysses: accurate detection of low-frequency structural variations in large insert-size sequencing libraries
A Gillet-Markowska, H Richard, G Fischer, I Lafontaine
Bioinformatics 31 (6), 801-808, 2014
142014
Parseq: reconstruction of microbial transcription landscape from RNA-Seq read counts using state-space models
B Mirauta, P Nicolas, H Richard
Bioinformatics 30 (10), 1409-1416, 2014
112014
Identification of programmed translational-1 frameshifting sites in the genome of Saccharomyces cerevisiae
M Bekaert, H Richard, B Prum, JP Rousset
Genome research 15 (10), 1411-1420, 2005
82005
seq++: analyzing biological sequences with a range of Markov-related models
V Miele, PY Bourguignon, D Robelin, G Nuel, H Richard
Bioinformatics 21 (11), 2783-2784, 2005
82005
SIC: a tool to detect short inverted segments in a biological sequence
D Robelin, H Richard, B Prum
Nucleic acids research 31 (13), 3669-3671, 2003
62003
SPA: simple web tool to assess statistical significance of DNA patterns
H Richard, G Nuel
Nucleic acids research 31 (13), 3679-3681, 2003
42003
DiNAMO: highly sensitive DNA motif discovery in high-throughput sequencing data
C Saad, L Noé, H Richard, J Leclerc, MP Buisine, H Touzet, M Figeac
BMC bioinformatics 19 (1), 223, 2018
32018
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