about
Relationship estimation from whole-genome sequence dataOrganization and evolution of olfactory receptor genes on human chromosome 11Whole-Genome Shotgun Assembly and Analysis of the Genome of Fugu rubripesAnalysis of genetic inheritance in a family quartet by whole-genome sequencingInitial sequencing and comparative analysis of the mouse genomeSequence analysis in the olfactory receptor gene cluster on human chromosome 17: recombinatorial events affecting receptor diversityThe evolution of vertebrate Toll-like receptorsChromosomal haplotypes by genetic phasing of human familiesGenetic mapping at 3-kilobase resolution reveals inositol 1,4,5-triphosphate receptor 3 as a risk factor for type 1 diabetes in SwedenA third approach to gene prediction suggests thousands of additional human transcribed regionsA novel Fanconi anaemia subtype associated with a dominant-negative mutation in RAD51Mutations in NOTCH1 cause Adams-Oliver syndromeHeterozygous Loss-of-Function Mutations in DLL4 Cause Adams-Oliver SyndromeGenetic divergence of the rhesus macaque major histocompatibility complexOrigin of the PSEN1 E280A mutation causing early-onset Alzheimer's diseaseCrowdsourced direct-to-consumer genomic analysis of a family quartetLow budget analysis of Direct-To-Consumer genomic testing familial dataAlternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF RegistryAn international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge.The olfactory receptor gene superfamily: data mining, classification, and nomenclature.A unified test of linkage analysis and rare-variant association for analysis of pedigree sequence data.Identification of copy number variants in whole-genome data using Reference Coverage Profiles.The genomic structure of human olfactory receptor genes.Personalized nutrition through big data.Genomic complexity of the variable region-containing chitin-binding proteins in amphioxusEvolutionary history of Tibetans inferred from whole-genome sequencing.Structural and genetic diversity of group B streptococcus capsular polysaccharides.Realistic artificial DNA sequences as negative controls for computational genomics.Sequence, structure, and evolution of a complete human olfactory receptor gene cluster.Comparative genomics of the human and mouse T cell receptor loci.The RUNX3 gene--sequence, structure and regulated expression.Kaviar: an accessible system for testing SNV novelty.P4 medicine: how systems medicine will transform the healthcare sector and society.Genome dynamics, evolution, and protein modeling in the olfactory receptor gene superfamily.Whole-genome sequencing of the world's oldest peopleWhole-genome haplotyping approaches and genomic medicine.Optimal scaling of digital transcriptomesAccurate and robust prediction of genetic relationship from whole-genome sequences.Systems genomics evaluation of the SH-SY5Y neuroblastoma cell line as a model for Parkinson's disease.Rare variants in neuronal excitability genes influence risk for bipolar disorder.
P50
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P50
description
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հետազոտող
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name
Gustavo Glusman
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Gustavo Glusman
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Gustavo Glusman
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Gustavo Glusman
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Gustavo Glusman
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Gustavo Glusman
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גוסטבו גלוסמן
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Gustavo Glusman
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Gustavo Glusman
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Gustavo Glusman
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Gustavo Glusman
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Gustavo Glusman
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Gustavo Glusman
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גוסטבו גלוסמן
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Gustavo Glusman
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Gustavo Glusman
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Gustavo Glusman
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Gustavo Glusman
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Gustavo Glusman
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Gustavo Glusman
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גוסטבו גלוסמן
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P106
P21
P2798
P31
P4012
P496
0000-0001-8060-5955