Machine Learning-Based Approach Highlights the Use of a Genomic Variant Profile for Precision Medicine in Ovarian Failure

Ovarian failure (OF) is a common cause of infertility usually diagnosed as idiopathic, with genetic causes accounting for 10–25% of cases. Whole-exome sequencing (WES) may enable identifying contributing genes and variant profiles to stratify the population into subtypes of OF. This study sought to...

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Detalles Bibliográficos
Autores principales: Henarejos-Castillo, Ismael, Aleman, Alejandro, Martinez-Montoro, Begoña, Gracia-Aznárez, Francisco Javier, Sebastian-Leon, Patricia, Romeu, Monica, Remohi, Jose, Patiño-Garcia, Ana, Royo, Pedro, Alkorta-Aranburu, Gorka, Diaz-Gimeno, Patricia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8305607/
https://www.ncbi.nlm.nih.gov/pubmed/34199109
http://dx.doi.org/10.3390/jpm11070609

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8305607/
https://www.ncbi.nlm.nih.gov/pubmed/34199109
http://dx.doi.org/10.3390/jpm11070609

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