Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Frederic Escudie"'
Autor:
Guillaume Labrousse, Pierre Vande Perre, Genis Parra, Marion Jaffrelot, Laura Leroy, Frederic Chibon, Frederic Escudie, Janick Selves, Jean-Sebastien Hoffmann, Rosine Guimbaud, Malik Lutzmann
Publikováno v:
NAR Cancer. 5
The exonuclease domain of DNA polymerases epsilon's catalytic subunit (POLE) removes misincorporated nucleotides, called proofreading. POLE-exonuclease mutations cause colorectal- and endometrial cancers with an extreme burden of single nucleotide su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f762d3fdfc4c84e011c3eeaa084cf5bd
https://doi.org/10.1093/narcan/zcad011
https://doi.org/10.1093/narcan/zcad011
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Solène M. Evrard, Sarah Péricart, David Grand, Nadia Amara, Frédéric Escudié, Julia Gilhodes, Pierre Bories, Alexandra Traverse-Glehen, Romain Dubois, Pierre Brousset, Marie Parrens, Camille Laurent
Publikováno v:
Haematologica, Vol 104, Iss 4 (2019)
Externí odkaz:
https://doaj.org/article/b1ad9263ad50405ea72343a5c60d3990
Publikováno v:
PeerJ, Vol 5, p e2988 (2017)
Background De novo transcriptome assembly of short reads is now a common step in expression analysis of organisms lacking a reference genome sequence. Several software packages are available to perform this task. Even if their results are of good qua
Externí odkaz:
https://doaj.org/article/6f05f9f61036480b81de3015a0d071a3
Genome-Wide Study of Structural Variants in Bovine Holstein, Montbéliarde and Normande Dairy Breeds.
Autor:
Mekki Boussaha, Diane Esquerré, Johanna Barbieri, Anis Djari, Alain Pinton, Rabia Letaief, Gérald Salin, Frédéric Escudié, Alain Roulet, Sébastien Fritz, Franck Samson, Cécile Grohs, Maria Bernard, Christophe Klopp, Didier Boichard, Dominique Rocha
Publikováno v:
PLoS ONE, Vol 10, Iss 8, p e0135931 (2015)
High-throughput sequencing technologies have offered in recent years new opportunities to study genome variations. These studies have mostly focused on single nucleotide polymorphisms, small insertions or deletions and on copy number variants. Other
Externí odkaz:
https://doaj.org/article/bfa56f7676a8444db34e58b4ea11367d