![Foto de Jorge](/img/nophoto.png)
Jorge
Amigo Lechuga
Publikationen, an denen er mitarbeitet Jorge Amigo Lechuga (21)
2020
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A compilation of tri-allelic SNPs from 1000 Genomes and use of the most polymorphic loci for a large-scale human identification panel
Forensic Science International: Genetics, Vol. 46
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Broadening the Applicability of a Custom Multi-Platform Panel of Microhaplotypes: Bio-Geographical Ancestry Inference and Expanded Reference Data
Frontiers in Genetics, Vol. 11
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Building a custom large-scale panel of novel microhaplotypes for forensic identification using MiSeq and Ion S5 massively parallel sequencing systems
Forensic Science International: Genetics, Vol. 45
2017
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Whole Exome Sequencing reveals new candidate genes in host genomic susceptibility to Respiratory Syncytial Virus Disease
Scientific Reports, Vol. 7, Núm. 1
2015
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Completion of a worldwide reference panel of samples for an ancestry informative Indel assay
Forensic Science International: Genetics, Vol. 17, pp. 75-80
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Mitogenomes from The 1000 Genome Project reveal new Near Eastern features in present-day Tuscans
PLoS ONE, Vol. 10, Núm. 3
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Tetra-allelic SNPs: Informative forensic markers compiled from public whole-genome sequence data
Forensic Science International: Genetics, Vol. 19, pp. 100-106
2014
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A genome-wide study of modern-day Tuscans: Revisiting Herodotus's theory on the origin of the Etruscans
PLoS ONE, Vol. 9, Núm. 9
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Global population variability in Qiagen Investigator HDplex STRs
Forensic Science International: Genetics, Vol. 8, Núm. 1, pp. 36-43
2013
2012
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GDF: Dealing with high-throughput genotyping multiplatform data for medical and population genetic applications
Journal of Proteomics and Bioinformatics, Vol. 5, Núm. 1, pp. 1-6
2011
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Analysis of global variability in 15 established and 5 new European Standard Set (ESS) STRs using the CEPH human genome diversity panel
Forensic Science International: Genetics, Vol. 5, Núm. 3, pp. 155-169
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Call for participation in the neurogenetics consortium within the Human Variome Project
Neurogenetics, Vol. 12, Núm. 3, pp. 169-173
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ENGINES: Exploring single nucleotide variation in entire human genomes
BMC Bioinformatics, Vol. 12
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The impact of modern migrations on present-day multi-ethnic Argentina as recorded on the mitochondrial DNA genome
BMC Genetics, Vol. 12
2010
2009
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Viability of in-house datamarting approaches for population genetics analysis of SNP genotypes
BMC Bioinformatics
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pop.STR-An online population frequency browser for established and new forensic STRs
Forensic Science International: Genetics Supplement Series, Vol. 2, Núm. 1, pp. 361-362
2008
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SPSmart: Adapting population based SNP genotype databases for fast and comprehensive web access
BMC Bioinformatics, Vol. 9
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The SNPforID browser: An online tool for query and display of frequency data from the SNPforID project
International Journal of Legal Medicine, Vol. 122, Núm. 5, pp. 435-440