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1دورية أكاديمية
المؤلفون: Claudia Fontsere, Martin Kuhlwilm, Carlos Morcillo-Suarez, Marina Alvarez-Estape, Jack D. Lester, Paolo Gratton, Joshua M. Schmidt, Paula Dieguez, Thierry Aebischer, Paula Álvarez-Varona, Anthony Agbor, Samuel Angedakin, Alfred K. Assumang, Emmanuel A. Ayimisin, Emma Bailey, Donatienne Barubiyo, Mattia Bessone, Andrea Carretero-Alonso, Rebecca Chancellor, Heather Cohen, Emmanuel Danquah, Tobias Deschner, Andrew Dunn, Jef Dupain, Villard E. Egbe, Olga Feliu, Annemarie Goedmakers, Anne-Céline Granjon, Josephine Head, Daniela Hedwig, Veerle Hermans, R. Adriana Hernandez-Aguilar, Inaoyom Imong, Sorrel Jones, Jessica Junker, Parag Kadam, Mike Kaiser, Mbangi Kambere, Magloire V. Kambale, Ammie K. Kalan, Ivonne Kienast, Deo Kujirakwinja, Kevin Langergraber, Juan Lapuente, Bradley Larson, Anne Laudisoit, Kevin Lee, Manuel Llana, Miquel Llorente, Sergio Marrocoli, David Morgan, Felix Mulindahabi, Mizuki Murai, Emily Neil, Sonia Nicholl, Stuart Nixon, Emma Normand, Chris Orbell, Lucy J. Ormsby, Liliana Pacheco, Alex Piel, Laura Riera, Martha M. Robbins, Aaron Rundus, Crickette Sanz, Lilah Sciaky, Volker Sommer, Fiona A. Stewart, Nikki Tagg, Luc Roscelin Tédonzong, Els Ton, Joost van Schijndel, Virginie Vergnes, Erin G. Wessling, Jacob Willie, Roman M. Wittig, Yisa G. Yuh, Kyle Yurkiw, Klaus Zuberbuehler, Jochen Hecht, Linda Vigilant, Christophe Boesch, Aida M. Andrés, David A. Hughes, Hjalmar S. Kühl, Esther Lizano, Mimi Arandjelovic, Tomas Marques-Bonet
المصدر: Cell Genomics, Vol 2, Iss 6, Pp 100133- (2022)
مصطلحات موضوعية: chimpanzee, non-invasive samples, fecal samples, hybridization capture, population genetics, conservation genomics, Genetics, QH426-470, Internal medicine, RC31-1245
وصف الملف: electronic resource
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2
المؤلفون: Sergi Civit, Carlos Morcillo-Suarez, Morten E. Allentoft, Antonia Díaz-Carvajal, Imma Ollich-Castanyer, Toni de-Dios, Manuel Ferrando-Bernal, Sergi Valverde, Carles Lalueza-Fox, Pere Gelabert
المساهمون: Ministerio de Economía y Competitividad (España), Ministerio de Ciencia, Innovación y Universidades (España), Agencia Estatal de Investigación (España), European Commission, Agència de Gestió d'Ajuts Universitaris i de Recerca
المصدر: Scientific Reports, Vol 10, Iss 1, Pp 1-11 (2020)
Ferrando-Bernal, M, Morcillo-Suarez, C, de-Dios, T, Gelabert, P, Civit, S, Díaz-Carvajal, A, Ollich-Castanyer, I, Allentoft, M E, Valverde, S & Lalueza-Fox, C 2020, ' Mapping co-ancestry connections between the genome of a Medieval individual and modern Europeans ', Scientific Reports, vol. 10, 6843 . https://doi.org/10.1038/s41598-020-64007-2
Digital.CSIC. Repositorio Institucional del CSIC
instname
Dipòsit Digital de la UB
Universidad de Barcelona
Scientific Reportsمصطلحات موضوعية: Male, Evolution, Molecular biology, common, Genealogia, ADN fòssil, Population, Population genetics, lcsh:Medicine, Polymorphism, Single Nucleotide, Genome, Identity by descent, Genealogy, White People, Article, Ethnicity, Icelanders, Humans, Relacions intergeneracionals, DNA, Ancient, education, lcsh:Science, education.field_of_study, Multidisciplinary, lcsh:R, Genetic Variation, Intergenerational relations, History, Medieval, language.human_language, Europe, Ancient DNA, Geography, Fossil DNA, Evolutionary biology, common.group, Genetic structure, language, Female, lcsh:Q, Icelandic
وصف الملف: application/pdf
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المؤلفون: Brian W. Davis, Aitor Serres-Armero, Elaine A. Ostrander, Tomas Marques-Bonet, Inna S. Povolotskaya, Carlos Morcillo-Suarez, David Juan, Jocelyn Plassais
المساهمون: National Human Genome Research Institute (US), European Research Council, Ministerio de Ciencia, Innovación y Universidades (España), Agencia Estatal de Investigación (España), European Commission, Howard Hughes Medical Institute, Fundación 'la Caixa', Generalitat de Catalunya
المصدر: Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Genome Res
Digital.CSIC. Repositorio Institucional del CSIC
instnameمصطلحات موضوعية: DNA Copy Number Variations, Genome-wide association study, Biology, Genome, Polymorphism, Single Nucleotide, Structural variation, 03 medical and health sciences, 0302 clinical medicine, Dogs, Genetics, Animals, Copy-number variation, Gene, Genetics (clinical), 030304 developmental biology, 2. Zero hunger, 0303 health sciences, Genome assembly, Transcriptome assembly, Copy number variation, Research, Genomics, Phenotype, Rangifer tarandus, Variation (linguistics), Evolutionary biology, Trait, 030217 neurology & neurosurgery, Genome-Wide Association Study, Genome annotation
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4190b1a8072484ef00fbb7d361a9f0a4
https://ddd.uab.cat/record/256109 -
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المؤلفون: Edward Kong, Pascal Timshel, Danielle Posthuma, Tõnu Esko, Maël Lebreton, Kathleen Mullan Harris, Philipp Koellinger, Murray B. Stein, Abraham A. Palmer, Urs Fischbacher, Robert J. Ursano, Erdogan Taskesen, Peter Eibich, Paul R. H. J. Timmers, Anke R. Hammerschlag, Ann H. Caplin, Jian Yang, Sandra Sanchez-Roige, Peter K. Joshi, Matthias Sutter, Pierre Fontanillas, Chia-Yen Chen, Albert Hofman, Patrick Turley, David A. Hinds, Futao Zhang, David Cesarini, Christina M. Lill, Laura Buzdugan, Ville Karhunen, Abdel Abdellaoui, S. Fleur W. Meddens, Henning Tiemeier, Christian L. Zund, Gert G. Wagner, Richard Karlsson Linnér, Lars Bertram, David W. Clark, Roy Thurik, André G. Uitterlinden, Maciej Trzaskowski, Mohammad Arfan Ikram, David Laibson, Cornelius A. Rietveld, Arcadi Navarro, Ernst Fehr, Yang Wu, Matthew B. McQueen, Ronald C. Kessler, Magnus Johannesson, Patrick J. F. Groenen, Gregor Hasler, James F. Wilson, Daniel Schunk, Stephen P. Tino, Pietro Biroli, Mark Alan Fontana, Juan R. González, Meena Kumari, Gerardus A. Meddens, Jonathan P. Beauchamp, Michelle N. Meyer, Jason D. Boardman, James J. Lee, Carlos Morcillo-Suarez, Aaron Kleinman, Minna Männikkö, Andrew Conlin, Adam Auton, Tune H. Pers, Michel G. Nivard, Ronald de Vlaming, Jon White, Robert Karlsson, Daniel J. Benjamin, Maarten Kooyman, Jacob Gratten, Aysu Okbay, Remy Z. Levin, Melissa C. Smart, Harriet de Wit, Conor C. Dolan, Frank J. A. van Rooij, Patrik K. E. Magnusson, Sonia Jain, Rauli Svento, Klaus M. Schmidt, Dorret I. Boomsma, Gerard Muntané, James MacKillop, Robbee Wedow, Yanchun Bao
مصطلحات موضوعية: Genetics, 0303 health sciences, Gabaergic neurotransmission, Single-nucleotide polymorphism, Genome-wide association study, Biology, Phenotype, 03 medical and health sciences, 0302 clinical medicine, SNP, Gene, 030217 neurology & neurosurgery, 030304 developmental biology, Genetic association
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f79df5a4866a0b8fd800528cffbe195
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المؤلفون: Sören Sonnenburg, Thorsten Dickhaus, Ernst Fehr, Daniel Schunk, Klaus-Robert Müller, Marius Kloft, Xavier Farré, Juan Antonio Rodríguez, Urko M. Marigorta, Bettina Mieth, Robin Vobruba, Gilles Blanchard, Carlos Morcillo-Suarez, Arcadi Navarro
المساهمون: University of Zurich, Navarro, Arcadi, Technische Universität Berlin (TU), Humboldt-Universität zu Berlin, Universitat Pompeu Fabra [Barcelona] (UPF), TomTom, School of Electrical and Computer Engineering - Georgia Insitute of Technology (ECE GeorgiaTech), Georgia Institute of Technology [Atlanta], Universität Zürich [Zürich] = University of Zurich (UZH), Universität Bremen, Institut für Mathematik [Potsdam], Universität Potsdam, Johannes Gutenberg - Universität Mainz (JGU), Institució Catalana de Recerca i Estudis Avançats (ICREA), Barcelona Institute of Science and Technology (BIST), Korea University [Seoul], European Research Council, German Research Foundation, European Commission, Federal Ministry of Education and Research (Germany), Red Española de Esclerosis Múltiple, Instituto de Salud Carlos III, Instituto Nacional de Bioinformática (España), Ministerio de Economía y Competitividad (España), Ministry of Education, Science and Technology (South Korea), National Research Foundation of Korea
المصدر: Scientific Reports
Scientific Reports, Nature Publishing Group, 2016, 6 (1), ⟨10.1038/srep36671⟩
Recercat. Dipósit de la Recerca de Catalunya
instname
Digital.CSIC. Repositorio Institucional del CSICمصطلحات موضوعية: 0301 basic medicine, Statistical methods, Computer science, Genome-wide association study, Machine learning, computer.software_genre, Genome-wide association studies, Statistical power, Article, [INFO.INFO-AI]Computer Science [cs]/Artificial Intelligence [cs.AI], Set (abstract data type), 03 medical and health sciences, [INFO.INFO-LG]Computer Science [cs]/Machine Learning [cs.LG], [MATH.MATH-ST]Mathematics [math]/Statistics [math.ST], 10007 Department of Economics, Statistical significance, Replication (statistics), genome, Statistical hypothesis testing, Genetic association, 1000 Multidisciplinary, Multidisciplinary, business.industry, Computational science, Institut für Mathematik, 330 Economics, Support vector machine, 030104 developmental biology, Multiple comparisons problem, wide association studies, statistical methods, Artificial intelligence, business, computer
وصف الملف: combining_multiple_hypotheses_Fehr.pdf - application/pdf; application/pdf
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المؤلفون: Eva Julià, Montse Camiña-Tato, M.C. Edo, M. Fernández, Xavier Montalban, Carlos Morcillo-Suarez, Arcadi Navarro, Manuel Comabella
المصدر: Journal of Neuroimmunology. 222:70-75
مصطلحات موضوعية: Adult, Genetic Markers, Male, Oncology, Candidate gene, medicine.medical_specialty, Genotype, DNA Mutational Analysis, Immunology, Single-nucleotide polymorphism, Bioinformatics, Polymorphism, Single Nucleotide, Severity of Illness Index, Linkage Disequilibrium, Multiple Sclerosis, Relapsing-Remitting, Gene Frequency, Internal medicine, Humans, Immunology and Allergy, SNP, Medicine, Genetic Predisposition to Disease, Genetic Testing, Allele, Genetic testing, Genetic association, Caspase 8, medicine.diagnostic_test, business.industry, Multiple sclerosis, Homozygote, Haplotype, Middle Aged, Multiple Sclerosis, Chronic Progressive, medicine.disease, Haplotypes, Neurology, Disease Progression, Female, Neurology (clinical), business
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المؤلفون: Xavier Montalban, Montse Camiña-Tato, M. Fernández, Carlos Morcillo-Suarez, Arcadi Navarro, Alejandro Horga, Manuel Comabella
المصدر: Journal of Neuroimmunology. 213:142-147
مصطلحات موضوعية: Adult, Genetic Markers, Male, Multiple Sclerosis, Genotype, DNA Mutational Analysis, Immunology, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, Gene Frequency, Risk Factors, Genetic variation, Secondary Prevention, Genetic predisposition, Humans, Immunology and Allergy, SNP, Genetic Predisposition to Disease, Genetic Testing, Allele, Genetic association, Genetics, Polymorphism, Genetic, Haplotype, Middle Aged, Neoplasm Proteins, Haplotypes, Neurology, Female, Neurology (clinical)
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المؤلفون: José Antonio del Río, Carlos Morcillo-Suarez, Manuel Comabella, Eduard Sarró, Xavier Montalban, Sunny Malhotra, Ana Navarro, Joaquín Castilló, M Moreno, Ramil N. Nurtdinov
المساهمون: European Commission, Red Española de Esclerosis Múltiple, Instituto de Salud Carlos III, Ministerio de Ciencia e Innovación (España), Generalitat de Catalunya
المصدر: Digital.CSIC. Repositorio Institucional del CSIC
instnameمصطلحات موضوعية: Adult, Male, Genotype, USP18 polymorphisms, Drug Resistance, Gene Expression, Real-Time Polymerase Chain Reaction, Peripheral blood mononuclear cell, Polymorphism, Single Nucleotide, Pathogenesis, Multiple sclerosis, Multiple Sclerosis, Relapsing-Remitting, Polymorphism (computer science), Interferon, Gene expression, Endopeptidases, Genetic susceptibility, Medicine, Humans, Immunologic Factors, Genetic Predisposition to Disease, Ubiquitins, business.industry, Interferon-beta, medicine.disease, ISG15, Real-time polymerase chain reaction, Treatment Outcome, Neurology, Immunology, Cytokines, Interferon-β, Response to treatment, Female, Neurology (clinical), business, Transcriptome, Ubiquitin Thiolesterase, medicine.drug
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المؤلفون: Arcadi Navarro, Guillermo Pita, Josep Alegre, Ángel Carreño-Torres, Núria Malats, Ignacio Medina, Joaquín Dopazo, Belen Lorente-Galdos, David G. Pisano, Ricardo Sangrós, Carlos Morcillo-Suarez, Txema Heredia, Gemma Vellalta
المصدر: Digital.CSIC. Repositorio Institucional del CSIC
instname
International Journal of Data Mining and Bioinformatics
r-CIPF: Repositorio Institucional Producción Científica del Centro de Investigación Principe Felipe (CIPF)
Centro de Investigación Principe Felipe (CIPF)
r-CIPF. Repositorio Institucional Producción Científica del Centro de Investigación Principe Felipe (CIPF)مصطلحات موضوعية: tag-SNPs, Genome-wide association study, SNP-arrays, PUPASuite, Single-nucleotide polymorphism, Computational biology, Library and Information Sciences, Biology, Polymorphism, Single Nucleotide, General Biochemistry, Genetics and Molecular Biology, Association, Databases, Genetic, Tagger, Linkage disequilibrium, SNP, PupaSuite, Selection (genetic algorithm), Genetic association, Genetics, Internet, complex disease, Genomics, Sequence Analysis, DNA, Single nucleotide polymorphisms, Tag SNP, SNP genotyping, Complex diseases, Algorithms, Software, Information Systems, SNPs
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf3e48416d9ae36fc7568b56128888b3
http://hdl.handle.net/10261/115846 -
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المصدر: Bioinformatics for Personalized Medicine ISBN: 9783642280610
JBIمصطلحات موضوعية: NetCDF, End results, Biological data, Database, business.industry, Computer science, computer.file_format, computer.software_genre, Data science, Software, Data format, Computer data storage, Leverage (statistics), business, Raw data, computer
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::7f1fed6a6ec8e2de806b85e7e49f05a5
https://doi.org/10.1007/978-3-642-28062-7_2