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Author Details

George Asimenos
2005
7
7
PMIDPaper TitleJournal TitlePublished Year
30858580Best practices for benchmarking germline small-variant calls in human genomes.Nat Biotechnol2019
30858580Best practices for benchmarking germline small-variant calls in human genomes.Nat Biotechnol2019
30899106Author Correction: Best practices for benchmarking germline small-variant calls in human genomes.Nat Biotechnol2019
30899106Author Correction: Best practices for benchmarking germline small-variant calls in human genomes.Nat Biotechnol2019
27099173A research roadmap for next-generation sequencing informatics.Sci Transl Med2016
27099173A research roadmap for next-generation sequencing informatics.Sci Transl Med2016
19378139Multiple alignment of DNA sequences with MAFFT.Methods Mol Biol2009
19378139Multiple alignment of DNA sequences with MAFFT.Methods Mol Biol2009
17567995Analyses of deep mammalian sequence alignments and constraint predictions for 1% of the human genome.Genome Res2007
17567995Analyses of deep mammalian sequence alignments and constraint predictions for 1% of the human genome.Genome Res2007
17571346Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project.Nature2007
17571346Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project.Nature2007
15965027Distribution and intensity of constraint in mammalian genomic sequence.Genome Res2005
15965027Distribution and intensity of constraint in mammalian genomic sequence.Genome Res2005
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Collaborators

Co-authored papers 4
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Co-authored papers 3
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National Human Genome Research Institute, National Institutes of Health
Co-authored papers 3
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HudsonAlpha Institute for Biotechnology
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Novartis Pharma AG
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Johns Hopkins University
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Genomics Institute, University of California Santa Cruz
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University of California berkeley
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Harvard University
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Co-authored papers 2
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Stanford University School of Medicine
Co-authored papers 2
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Partners Healthcare Center for Personalized Genetic Medicine
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