F. M. Jabato

发表

Systematic identification of genetic systems associated with phenotypes in patients with rare genomic copy number variations

F. Pazos, J. A. Ranea, M. Chagoyen, 2020, Human Genetics.

Phenotype-genotype comorbidity analysis of patients with rare disorders provides insight into their pathological and molecular bases

F. Pazos, J. A. Ranea, F. M. Jabato, 2020, PLoS genetics.

An improved de novo assembling and polishing of Solea senegalensis transcriptome shed light on retinoic acid signalling in larvae

M. Claros, F. M. Jabato, Pedro Seoane, 2020, Scientific Reports.

Assigning protein function from domain-function associations using DomFun

C. Orengo, J. A. Ranea, I. Sillitoe, 2020, BMC Bioinform..

Gene expression analysis method integration and co-expression module detection applied to rare glucide metabolism disorders using ExpHunterSuite

F. M. Jabato, Pedro Seoane, J. Perkins, 2021, Scientific Reports.

Evaluating, Filtering and Clustering Genetic Disease Cohorts Based on Human Phenotype Ontology Data with Cohort Analyzer

F. M. Jabato, J. Perkins, E. Rojano, 2021, Journal of personalized medicine.

Transcriptional changes in dendritic cells underlying allergen specific induced tolerance in a mouse model

F. M. Jabato, Pedro Seoane, J. Perkins, 2022, Scientific Reports.

Comprehensive Analysis of Patients with Undiagnosed Genetic Diseases Using the Patient Exploration Tools Suite (PETS)

Juan Garcia Ranea, Elena Rojano, Pedro Seoane-Zonjic, 2020, IWBBIO.

Assigning protein function from domain-function associations using DomFun

C. Orengo, J. A. Ranea, I. Sillitoe, 2022, BMC Bioinformatics.