Gholson J. Lyon mainly focuses on Genetics, Exome sequencing, Exome, DNA sequencing and Genomics. Genetics and Enzyme are commonly linked in his work. Gholson J. Lyon combines subjects such as Acetyltransferase, Ogden Syndrome, Hypotonia, X chromosome and Exon with his study of Exome sequencing.
His Exome research incorporates elements of Genome, Whole genome sequencing, Sequence alignment and Indel. His DNA sequencing research incorporates themes from Data mining, Deep sequencing and Word error rate. His Genomics research includes themes of Ontology, Precision medicine, Translational research and Phenotype.
His scientific interests lie mostly in Genetics, Computational biology, Exome sequencing, Genome and Whole genome sequencing. All of his Genetics and DNA sequencing, Copy-number variation, Human genetics, Genomics and Personal genomics investigations are sub-components of the entire Genetics study. His Copy-number variation research is multidisciplinary, relying on both Genome-wide association study and Tourette syndrome.
His study in Exome sequencing is interdisciplinary in nature, drawing from both Hypotonia, Human Phenotype Ontology and Indel. The Genome study combines topics in areas such as Genotyping and Bioinformatics. His research investigates the link between Whole genome sequencing and topics such as Exome that cross with problems in Human genome.
Gholson J. Lyon spends much of his time researching Genetics, Exome sequencing, Tourette syndrome, Phenotype and Human Phenotype Ontology. His study in Copy-number variation, Genomics, Intellectual disability, Human genetics and NAA15 falls within the category of Genetics. His Genomics research is multidisciplinary, incorporating perspectives in Translational research, Human genome, Computational biology and Candidate gene.
The concepts of his Candidate gene study are interwoven with issues in Indel, Annotation, Molecular Sequence Annotation, INDEL Mutation and DNA sequencing. His work deals with themes such as Missense mutation, Contig, Allele and Bioinformatics, which intersect with Exome sequencing. Gholson J. Lyon has included themes like Clinical psychology, Attention deficit hyperactivity disorder, Tics and Genetic architecture in his Tourette syndrome study.
Gholson J. Lyon mainly investigates Genetics, Tourette syndrome, Computational biology, Genome-wide association study and Attention deficit hyperactivity disorder. His work in Exome sequencing, Missense mutation, Shotgun sequencing, Reference genome and Sequence assembly is related to Genetics. His research in Exome sequencing is mostly concerned with Cancer genome sequencing.
His work carried out in the field of Tourette syndrome brings together such families of science as Tics, Proband and Copy-number variation. His studies deal with areas such as Indel, Human genome, Sequencing data and Genomics as well as Computational biology. Gholson J. Lyon interconnects Annotation, INDEL Mutation, DNA sequencing and Candidate gene in the investigation of issues within Genomics.
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The Human Phenotype Ontology in 2017
Sebastian Köhler;Nicole A. Vasilevsky;Mark Engelstad;Erin D. Foster.
Nucleic Acids Research (2017)
Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2 , a COX assembly gene
L C Papadopoulou;C M Sue;M M Davidson;K Tanji.
Nature Genetics (1999)
Analysis of shared heritability in common disorders of the brain
Verneri Anttila;Verneri Anttila;Brendan Bulik-Sullivan;Brendan Bulik-Sullivan;Hilary K. Finucane;Raymond K. Walters;Raymond K. Walters.
Low concordance of multiple variant-calling pipelines: practical implications for exome and genome sequencing
Jason O'Rawe;Jason O'Rawe;Tao Jiang;Guangqing Sun;Yiyang Wu;Yiyang Wu.
Genome Medicine (2013)
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge.
Catherine A. Brownstein;Alan H. Beggs;Nils Homer;Barry Merriman.
Peptide signaling in Staphylococcus aureus and other Gram-positive bacteria.
Gholson J. Lyon;Richard P. Novick.
Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder
Josephine Elia;Joseph T. Glessner;Kai Wang;Nagahide Takahashi.
Nature Genetics (2012)
Rational design of a global inhibitor of the virulence response in Staphylococcus aureus, based in part on localization of the site of inhibition to the receptor-histidine kinase, AgrC
Gholson J. Lyon;Patricia Mayville;Tom W. Muir;Richard P. Novick.
Proceedings of the National Academy of Sciences of the United States of America (2000)
Lifetime Prevalence, Age of Risk, and Genetic Relationships of Comorbid Psychiatric Disorders in Tourette Syndrome
Matthew E. Hirschtritt;Paul C. Lee;David L. Pauls;Yves Dion.
JAMA Psychiatry (2015)
Exfoliatin-producing strains define a fourth agr specificity group in Staphylococcus aureus.
S. Jarraud;G. J. Lyon;G. J. Lyon;A. M. S. Figueiredo;G. Lina.
Journal of Bacteriology (2000)
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