نتائج البحث - "Fernando M. Jabato"

المساهمون: Ministerio de Economía y Competitividad (España), Junta de Andalucía, Instituto de Salud Carlos III, Fundación Ramón Areces, National Institutes of Health (US), Fundación Progreso y Salud, Comunidad de Madrid, Fundación Isabel Gemio, Sanz, Pascual, La Caixa, Centro de Investigación Biomédica en Red Enfermedades Raras (España), Sanz, Pascual [0000-0002-2399-4103]

المصدر: Digital.CSIC. Repositorio Institucional del CSIC
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Scientific Reports, Vol 11, Iss 1, Pp 1-12 (2021)
Scientific Reports

مصطلحات موضوعية: Cellular signalling networks, Statistical methods, Computer science, Science, Metabolic disorders, Arabidopsis, Multiple methods, computer.software_genre, Article, Bioconductor, 03 medical and health sciences, Naive Bayes classifier, Gene expression analysis, Rare Diseases, 0302 clinical medicine, Code (cryptography), Computational models, Humans, RNA-Seq, Transcriptomics, Immune cell infiltration, 030304 developmental biology, 0303 health sciences, Multidisciplinary, Gene Expression Profiling, Bayes Theorem, Expression (mathematics), Computational biology and bioinformatics, Metabolism disorder, Mechanisms of disease, Gene Expression Regulation, Scalability, Medicine, Calcium Channels, Data mining, computer, Neurological disorders, Algorithms, Software, 030217 neurology & neurosurgery

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URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::326e6b3334ca56632988cbeb8fa22d0a
https://doi.org/10.1038/s41598-021-94343-w

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7

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

المؤلفون: James R. Perkins, Pedro Seoane, José Córdoba-Caballero, Manuel Manchado, M. Gonzalo Claros, Fernando M. Jabato

المصدر: Scientific Reports
Scientific Reports, Vol 10, Iss 1, Pp 1-17 (2020)

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URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2983e4aaf2988e952713d88f6e524418
http://europepmc.org/articles/PMC7691524

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8

Assigning protein function from domain-function associations using DomFun

المؤلفون: Elena Rojano, Fernando M. Jabato, James R. Perkins, José Córdoba-Caballero, Federico García-Criado, Ian Sillitoe, Christine Orengo, Juan A. G. Ranea, Pedro Seoane-Zonjic

المصدر: BMC Bioinformatics
BMC Bioinformatics, Vol 23, Iss 1, Pp 1-19 (2022)

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URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::011b39ad9e0adcbe9748f2ba6f533742
https://pubmed.ncbi.nlm.nih.gov/35033002

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9

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

المؤلفون: Florencio Pazos, Elena Rojano, Fernando M. Jabato, Elena Díaz-Santiago, James R. Perkins, Pedro Seoane, Juan A. G. Ranea

المساهمون: Ministerio de Ciencia, Innovación y Universidades (España), Agencia Estatal de Investigación (España), Junta de Andalucía, European Commission, Fundación Progreso y Salud, Fundación Ramón Areces, Universidad de Málaga, Instituto de Salud Carlos III

المصدر: PLoS Genetics, Vol 16, Iss 10, p e1009054 (2020)
Digital.CSIC. Repositorio Institucional del CSIC
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PLoS Genetics

مصطلحات موضوعية: Cancer Research, Comorbidity, QH426-470, Biochemistry, Genome, Database and Informatics Methods, 0302 clinical medicine, DiGeorge syndrome, Databases, Genetic, Copy-number variation, Genetics (clinical), 0303 health sciences, Genomics, Phenotype, Phenotypes, DECIPHER, Research Article, DNA Copy Number Variations, Genotype, Gene prediction, Computational biology, Biology, Research and Analysis Methods, 03 medical and health sciences, Rare Diseases, Protein Domains, medicine, Genetics, Homeobox, Humans, Genetic Predisposition to Disease, Gene Prediction, Molecular Biology Techniques, Molecular Biology, Genetic Association Studies, Ecology, Evolution, Behavior and Systematics, 030304 developmental biology, Genome, Human, Gene Mapping, Biology and Life Sciences, Computational Biology, Proteins, Human Genetics, Genome Analysis, medicine.disease, Human genetics, Biological Databases, Mutation Databases, Genetics of Disease, Mutation, 030217 neurology & neurosurgery

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URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa1f47cd0269aee5d807d2142643b51c
https://doaj.org/article/6dd3ee164edf4928a8b351983cede7ae

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10

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

المؤلفون: Juan A. G. Ranea, Elena Rojano, James R. Perkins, Fernando M. Jabato, Pedro Seoane-Zonjic

المصدر: Bioinformatics and Biomedical Engineering ISBN: 9783030453848
IWBBIO

مصطلحات موضوعية: business.industry, Cohort, Intellectual disability, Genetic variants, Complex disease, Medicine, DECIPHER, In patient, business, Bioinformatics, medicine.disease, Genome, Pathological

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::e1948bf87e56894a427f0aa4cd1fd74b
https://doi.org/10.1007/978-3-030-45385-5_69

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