Jorge Amigo

Summary

Affiliation: Santiago de Compostela
Country: Spain

Publications

  1. pmc The impact of modern migrations on present-day multi-ethnic Argentina as recorded on the mitochondrial DNA genome
    María Laura Catelli
    Equipo Argentino de Antropología Forense, Independencia 644 5C, Edif EME1, Cordoba, Argentina
    BMC Genet 12:77. 2011
  2. pmc SPSmart: adapting population based SNP genotype databases for fast and comprehensive web access
    Jorge Amigo
    Spanish National Genotyping Center CeGen, Genomic Medicine Group, CIBERER, University of Santiago de Compostela, Galicia, Spain
    BMC Bioinformatics 9:428. 2008
  3. pmc Viability of in-house datamarting approaches for population genetics analysis of SNP genotypes
    Jorge Amigo
    Spanish National Genotyping Center CeGen, Genomic Medicine Group, CIBERER, University of Santiago de Compostela, Galicia, Spain
    BMC Bioinformatics 10:S5. 2009
  4. pmc ENGINES: exploring single nucleotide variation in entire human genomes
    Jorge Amigo
    Grupo de Medicina Xenómica, CIBERER, Universidade de Santiago de Compostela, Santiago de Compostela, Galicia, Spain
    BMC Bioinformatics 12:105. 2011
  5. doi The SNPforID browser: an online tool for query and display of frequency data from the SNPforID project
    Jorge Amigo
    Spanish National Genotyping Center CeGen and Genomic Medicine Group, CIBERER, University of Santiago de Compostela, Santiago de Compostela, Spain
    Int J Legal Med 122:435-40. 2008
  6. pmc A reduced number of mtSNPs saturates mitochondrial DNA haplotype diversity of worldwide population groups
    Antonio Salas
    Unidade de Xenetica, Departamento de Anatomía Patolóxica e Ciencias Forenses, Universidade de Santiago de Compostela, Galicia, Spain
    PLoS ONE 5:e10218. 2010
  7. ncbi A novel stop mutation in the vascular endothelial growth factor-C gene (VEGFC) results in Milroy-like disease
    Emilia Balboa-Beltran
    Fundacion Publica Galega de Medicina Xenomica, SERGAS, Santiago de Compostela, Spain
    J Med Genet 51:475-8. 2014
  8. pmc A generalized model to estimate the statistical power in mitochondrial disease studies involving 2×k tables
    Jacobo Pardo-Seco
    Unidade de Xenetica, Departamento de Anatomía Patolóxica e Ciencias Forenses, and Instituto de Ciencias Forenses, Grupo de Medicina Xenómica GMX, Facultade de Medicina, Universidade de Santiago de Compostela, Galicia, Spain
    PLoS ONE 8:e73567. 2013

Collaborators

  • Antonio Salas
  • Angel Carracedo
  • Christopher Phillips
  • Emilia Balboa-Beltran
  • Jacobo Pardo-Seco
  • María Laura Catelli
  • María J Fernández-Seara
  • Maria L Couce
  • Francisco Barros
  • Beatriz Sobrino
  • Alejandro Pérez-Muñuzuri
  • Carlos García-Magán
  • Ramón Lago
  • Wenceslao Gonzãlez-Manteiga
  • Alicia Borosky
  • Alberto Gómez-Carballa
  • Ana Mosquera-Miguel
  • Carola Romanini
  • Vanesa Alvarez-Iglesias
  • Carlos Vullo

Detail Information

Publications8

  1. pmc The impact of modern migrations on present-day multi-ethnic Argentina as recorded on the mitochondrial DNA genome
    María Laura Catelli
    Equipo Argentino de Antropología Forense, Independencia 644 5C, Edif EME1, Cordoba, Argentina
    BMC Genet 12:77. 2011
    ..A worldwide database was used for phylogeographic inferences, inter-population comparisons, and admixture analysis. Samples identified as belonging to hg (hg) H2a5 were sequenced for the entire mtDNA genome...
  2. pmc SPSmart: adapting population based SNP genotype databases for fast and comprehensive web access
    Jorge Amigo
    Spanish National Genotyping Center CeGen, Genomic Medicine Group, CIBERER, University of Santiago de Compostela, Galicia, Spain
    BMC Bioinformatics 9:428. 2008
    ....
  3. pmc Viability of in-house datamarting approaches for population genetics analysis of SNP genotypes
    Jorge Amigo
    Spanish National Genotyping Center CeGen, Genomic Medicine Group, CIBERER, University of Santiago de Compostela, Galicia, Spain
    BMC Bioinformatics 10:S5. 2009
    ..While many of these SNP repositories have implemented data retrieval tools for general-purpose mining, these alone cannot cover the broad spectrum of needs of most medical and population genetics studies...
  4. pmc ENGINES: exploring single nucleotide variation in entire human genomes
    Jorge Amigo
    Grupo de Medicina Xenómica, CIBERER, Universidade de Santiago de Compostela, Santiago de Compostela, Galicia, Spain
    BMC Bioinformatics 12:105. 2011
    ....
  5. doi The SNPforID browser: an online tool for query and display of frequency data from the SNPforID project
    Jorge Amigo
    Spanish National Genotyping Center CeGen and Genomic Medicine Group, CIBERER, University of Santiago de Compostela, Santiago de Compostela, Spain
    Int J Legal Med 122:435-40. 2008
    ..The interface has been designed to offer the useful facility of combining populations into appropriate geographic groups for visual comparison of populations individually or amongst user-defined groupings and with equivalent HapMap data...
  6. pmc A reduced number of mtSNPs saturates mitochondrial DNA haplotype diversity of worldwide population groups
    Antonio Salas
    Unidade de Xenetica, Departamento de Anatomía Patolóxica e Ciencias Forenses, Universidade de Santiago de Compostela, Galicia, Spain
    PLoS ONE 5:e10218. 2010
    ..Applications of the selected mtSNP panel range from anthropologic and medical studies to forensic genetic casework...
  7. ncbi A novel stop mutation in the vascular endothelial growth factor-C gene (VEGFC) results in Milroy-like disease
    Emilia Balboa-Beltran
    Fundacion Publica Galega de Medicina Xenomica, SERGAS, Santiago de Compostela, Spain
    J Med Genet 51:475-8. 2014
    ..The only genetic alteration known to be associated with Milroy-like disease was recently identified in a family with a frameshift mutation in vascular endothelial growth factor C (VEGFC) gene, which encodes a VEGFR3 ligand...
  8. pmc A generalized model to estimate the statistical power in mitochondrial disease studies involving 2×k tables
    Jacobo Pardo-Seco
    Unidade de Xenetica, Departamento de Anatomía Patolóxica e Ciencias Forenses, and Instituto de Ciencias Forenses, Grupo de Medicina Xenómica GMX, Facultade de Medicina, Universidade de Santiago de Compostela, Galicia, Spain
    PLoS ONE 8:e73567. 2013
    ..haplogroups) has been analyzed in regards to a number of multifactorial diseases. The statistical power of a case-control study determines the a priori probability to reject the null hypothesis of homogeneity between cases and controls...