Zobrazeno 1 - 10
of 17
pro vyhledávání: '"María Inés Fariello"'
Autor:
Christian Fachola, Agustín Tornaría, Paola Bermolen, Germán Capdehourat, Lorena Etcheverry, María Inés Fariello
Publikováno v:
Data, Vol 8, Iss 2, p 43 (2023)
Federated learning techniques aim to train and build machine learning models based on distributed datasets across multiple devices while avoiding data leakage. The main idea is to perform training on remote devices or isolated data centers without tr
Externí odkaz:
https://doaj.org/article/e05ba71fa65f4533981adbf3844563f9
Publikováno v:
PLoS ONE, Vol 17, Iss 8, p e0271097 (2022)
The ancestry of each locus of the genome can be estimated (local ancestry) based on sequencing or genotyping information together with reference panels of ancestral source populations. The length of those ancestry-specific genomic segments are common
Externí odkaz:
https://doaj.org/article/7a7cccc8437048b4bf302f6c4c665914
Autor:
Lucía Spangenberg, María Inés Fariello, Darío Arce, Gabriel Illanes, Gonzalo Greif, Jong-Yeon Shin, Seong-Keun Yoo, Jeong-Sun Seo, Carlos Robello, Changhoon Kim, John Novembre, Mónica Sans, Hugo Naya
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
The Amerindian group known as the Charrúas inhabited Uruguay at the timing of European colonial contact. Even though they were extinguished as an ethnic group as a result of a genocide, Charrúan heritage is part of the Uruguayan identity both cultu
Externí odkaz:
https://doaj.org/article/f2310dc3e96d446fafe951ce1f0c1c71
Autor:
Rossina Novas, Magdalena Cardenas-Rodriguez, Paola Lepanto, Matías Fabregat, Magela Rodao, María Inés Fariello, Mauricio Ramos, Camila Davison, Gabriela Casanova, Lucía Alfaya, Federico Lecumberry, Gualberto González-Sapienza, Florencia Irigoín, Jose L. Badano
Publikováno v:
Scientific Reports, Vol 8, Iss 1, Pp 1-16 (2018)
Abstract Bardet-Biedl syndrome (BBS) is a ciliopathy characterized by retinal degeneration, obesity, polydactyly, renal disease and mental retardation. CCDC28B is a BBS-associated protein that we have previously shown plays a role in cilia length reg
Externí odkaz:
https://doaj.org/article/b12b6dca1e794eb5831efb3cd8564235
Autor:
Matías Arim, Daniel Herrera-Esposito, Paola Bermolen, Álvaro Cabana, María Inés Fariello, Mauricio Lima, Hector Romero
Publikováno v:
Journal of theoretical biology. 542
Contact tracing, case isolation, quarantine, social distancing, and other non-pharmaceutical interventions (NPIs) have been a cornerstone in managing the COVID-19 pandemic. However, their effects on disease dynamics are not fully understood. Saturati
Autor:
Christophe Jacquet, Maxime Bonhomme, Marie-Laure Pilet-Nayel, Yacine Badis, Hélène Navier, Henri Miteul, Bernard Dumas, Ahmed Hajri, Deborah A. Samac, María Inés Fariello, Alain Baranger
Publikováno v:
Heredity (Edinb)
Heredity
Heredity, Nature Publishing Group, 2019, 123 (4), pp.517-531. ⟨10.1038/s41437-019-0235-x⟩
Heredity, Nature Publishing Group, 2019
Heredity, 2019, 123 (4), pp.517-531. ⟨10.1038/s41437-019-0235-x⟩
Heredity
Heredity, Nature Publishing Group, 2019, 123 (4), pp.517-531. ⟨10.1038/s41437-019-0235-x⟩
Heredity, Nature Publishing Group, 2019
Heredity, 2019, 123 (4), pp.517-531. ⟨10.1038/s41437-019-0235-x⟩
International audience; Quantitative trait loci (QTL) with small effects, which are pervasive in quantitative phenotypic variation, are difficult to detect in genome-wide association studies (GWAS). To improve their detection, we propose to use a loc
Autor:
Álvaro Cabana, Héctor Romero, María Inés Fariello, Daniel Herrera-Esposito, Mauricio Lima, Matías Arim, Paola Bermolen
Non-pharmaceutical interventions (NPIs) have been a cornerstone in managing emergent diseases such as COVID-191–4. However, despite their potential to contain or attenuate the epidemic, the effects of NPIs on disease dynamics are not well understoo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b9de1c95763a977b3b9dfa8a8cb0b22
https://doi.org/10.1101/2020.09.14.20194159
https://doi.org/10.1101/2020.09.14.20194159
Autor:
Federico Lecumberry, Lucía Alfaya, Camila Davison, Gabriela Casanova, Jose L. Badano, Paola Lepanto, Florencia Irigoín, Rossina Novas, Mauricio Ramos, María Inés Fariello, Magela Rodao, Matías Fabregat, Gualberto González-Sapienza, Magdalena Cardenas-Rodriguez
Publikováno v:
Scientific Reports, Vol 8, Iss 1, Pp 1-16 (2018)
Scientific Reports
COLIBRI
Universidad de la República
instacron:Universidad de la República
Scientific Reports
COLIBRI
Universidad de la República
instacron:Universidad de la República
Bardet-Biedl syndrome (BBS) is a ciliopathy characterized by retinal degeneration, obesity, polydactyly, renal disease and mental retardation. CCDC28B is a BBS-associated protein that we have previously shown plays a role in cilia length regulation w
Autor:
Patrice Dehais, María Inés Fariello, Olivier Bouchez, Frédérique Pitel, Simon Boitard, Julien Recoquillay, Thomas Faraut, Cécile Arnould, Sophie Leroux, David Robelin, Sabine Mercier, Magali SanCristobal, Christine Leterrier, David Gourichon, Gerald Salin
Publikováno v:
Molecular Ecology
Molecular Ecology, Wiley, 2017, 26 (14), pp.3700-3714. ⟨10.1111/mec.14141⟩
Molecular Ecology, Wiley, 2017, 26 (14), pp.3700-3714. 〈10.1111/mec.14141〉
Molecular Ecology, 2017, 26 (14), pp.3700-3714. ⟨10.1111/mec.14141⟩
Molecular Ecology, Wiley, 2017, 26 (14), pp.3700-3714. ⟨10.1111/mec.14141⟩
Molecular Ecology, Wiley, 2017, 26 (14), pp.3700-3714. 〈10.1111/mec.14141〉
Molecular Ecology, 2017, 26 (14), pp.3700-3714. ⟨10.1111/mec.14141⟩
Detecting genomic footprints of selection is an important step in the understanding of evolution. Accounting for linkage disequilibrium in genome scans increases detection power, but haplotype-based methods require individual genotypes and are not ap
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f989e8167cebc596ee2195241cfde43
https://hal.archives-ouvertes.fr/hal-01607837
https://hal.archives-ouvertes.fr/hal-01607837
Publikováno v:
Molecular and Cellular Probes. 28:175-180
Aberrant protein subcellular localization caused by mutation is a prominent feature of many human diseases. In Cystic Fibrosis (CF), a recessive lethal disorder that results from dysfunction of the Cystic Fibrosis Transmembrane Conductance Regulator