نتائج البحث - "Genome-Wide Association Study/standards"

المصدر: Andersen, L L, Terczyńska-Dyla, E, Mørk, N, Scavenius, C, Enghild, J J, Höning, K, Hornung, V, Christiansen, M, Mogensen, T H & Hartmann, R 2019, ' Frequently used bioinformatics tools overestimate the damaging effect of allelic variants ', Genes and Immunity, vol. 20, no. 1, pp. 10-22 . https://doi.org/10.1038/s41435-017-0002-zTest

مصطلحات موضوعية: Male, 0301 basic medicine, Encephalitis, Herpes Simplex/genetics, Genome-Wide Association Study/standards, Immunology, Mutation, Missense, Single-nucleotide polymorphism, Genome-wide association study, Biology, Bioinformatics, Polymorphism, Single Nucleotide, 03 medical and health sciences, 0302 clinical medicine, Genetics, medicine, False positive paradox, Humans, Missense mutation, False Positive Reactions, Genetic Testing, Receptors, Cytokine, Allele, Child, Genetic Testing/standards, Gene, Genetics (clinical), Receptors, Interferon, Genetic testing, medicine.diagnostic_test, Receptors, Cytokine/genetics, Computational Biology, HEK293 Cells, 030104 developmental biology, Mutation (genetic algorithm), Software/standards, Female, Encephalitis, Herpes Simplex, Computational Biology/standards, Software, Genome-Wide Association Study, 030215 immunology

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3dfa079599c7d0dd0a45a7a36caaa35eTest
https://doi.org/10.1038/s41435-017-0002-zTest

6

دورية أكاديمية

Frequently used bioinformatics tools overestimate the damaging effect of allelic variants

المؤلفون: Andersen, Line Lykke, Terczyńska-Dyla, Ewa, Mørk, Nanna, Scavenius, Carsten, Enghild, Jan J, Höning, Klara, Hornung, Veit, Christiansen, Mette, Mogensen, Trine H, Hartmann, Rune

المصدر: Andersen , L L , Terczyńska-Dyla , E , Mørk , N , Scavenius , C , Enghild , J J , Höning , K , Hornung , V , Christiansen , M , Mogensen , T H & Hartmann , R 2019 , ' Frequently used bioinformatics tools overestimate the damaging effect of allelic variants ' , Genes and Immunity , vol. 20 , no. 1 , pp. 10-22 . https://doi.org/10.1038/s41435-017-0002-zTest

مصطلحات موضوعية: Child, Computational Biology/standards, Encephalitis, Herpes Simplex/genetics, False Positive Reactions, Female, Genetic Testing/standards, Genome-Wide Association Study/standards, HEK293 Cells, Humans, Male, Mutation, Missense, Polymorphism, Single Nucleotide, Receptors, Cytokine/genetics, Software/standards

العلاقة: https://pure.au.dk/portal/en/publications/c945d13c-4430-4551-bda9-2f1e60cb7ffcTest

الإتاحة: https://doi.org/10.1038/s41435-017-0002-zTest
https://pure.au.dk/portal/en/publications/c945d13c-4430-4551-bda9-2f1e60cb7ffcTest

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7

دورية أكاديمية

Assessment and characterization of phenotypic heterogeneity of anxiety disorders across five large cohorts.

المؤلفون: Lee, M., Aggen, S.H., Otowa, T., Castelao, E., Preisig, M., Grabe, H.J., Hartman, C.A., Oldehinkel, A.J., Middeldorp, C.M., Tiemeier, H., Hettema, J.M.

المصدر: International journal of methods in psychiatric research, vol. 25, no. 4, pp. 255-266

مصطلحات موضوعية: Adult, Aged, Anxiety Disorders/diagnosis, Cohort Studies, Female, Genome-Wide Association Study/standards, Humans, Male, Meta-Analysis as Topic, Middle Aged, Phenotype, anxiety disorder, factor analysis, measurement invariance

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/27417386; info:eu-repo/semantics/altIdentifier/eissn/1557-0657; https://serval.unil.ch/notice/serval:BIB_3FF1303159F0Test; urn:issn:1049-8931

الإتاحة: https://doi.org/10.1002/mpr.1519Test
https://serval.unil.ch/notice/serval:BIB_3FF1303159F0Test

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النص الكامل

8

Expectations and challenges stemming from genome-wide association studies

المؤلفون: Paul Brennan, Paolo Vineis, Federico Canzian, Marylyn D. Ritchie, Ulf Strömberg, John F. Thompson, John P. A. Ioannidis, Giuseppe Matullo, Emanuela Taioli

المصدر: Mutagenesis. 23:439-444

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e6c0398de16b59967cadda1160324d8Test
https://doi.org/10.1093/mutage/gen042Test

9

Genome-wide DNA methylation detection by MethylCap-seq and Infinium HumanMethylation450 BeadChips: an independent large-scale comparison

المؤلفون: Jocelyne Bloch, Sebastian Kurscheid, Tim De Meyer, Roger Stupp, Geert Trooskens, Monika E. Hegi, Pierre Bady, Mauro Delorenzi, Johan M. Kros, Wim Van Criekinge, Johannes A. Hainfellner

المساهمون: Pathology, University of Zurich, Hegi, Monika E

المصدر: Sci Rep
Scientific Reports
Scientific Reports, 5:15375. Nature Publishing Group
Scientific Reports, vol. 5, pp. 15375
SCIENTIFIC REPORTS

مصطلحات موضوعية: Epigenomics, GLIOBLASTOMA, Genome-wide association study, 610 Medicine & health, Computational biology, SUBSET-QUANTILE, Biology, HIGH-THROUGHPUT, Sensitivity and Specificity, Article, Epigenesis, Genetic, NORMALIZATION, MICROARRAY, Humans, Methylated DNA immunoprecipitation, Alleles, Genetics, 1000 Multidisciplinary, SITES, Multidisciplinary, Biology and Life Sciences, Computational Biology, Molecular Sequence Annotation, Gold standard (test), DNA Methylation, ADJUVANT TEMOZOLOMIDE, CANCER, Biomarker (cell), Case-Control Studies, Computational Biology/methods, CpG Islands, Epigenomics/methods, Epigenomics/standards, Genome-Wide Association Study/methods, Genome-Wide Association Study/standards, Glioblastoma/genetics, Differentially methylated regions, DNA methylation, 10032 Clinic for Oncology and Hematology, Illumina Methylation Assay, ARRAY, Glioblastoma, PACKAGE, Genome-Wide Association Study

وصف الملف: application/pdf; srep15375.pdf - application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33596876b31d71154f41ca050463e3b5Test
https://pure.eur.nl/en/publications/bbe62b33-bd6e-45d9-87fe-df171f80b2e5Test

10

دورية أكاديمية

From genome-wide association studies to next-generation sequencing: lessons from the past and planning for the future.

المؤلفون: Sharma, Manu, Krüger, Rejko, Gasser, Thomas

المصدر: JAMA neurology 71(1), 5 (2014). doi:10.1001/jamaneurol.2013.3682

مصطلحات موضوعية: info:eu-repo/classification/ddc/610, Alzheimer Disease: genetics, Forecasting: methods, Genetic Predisposition to Disease, Genome-Wide Association Study: methods, Genome-Wide Association Study: standards, Genome-Wide Association Study: trends, Humans, Parkinson Disease: genetics, Sequence Analysis, DNA: trends

جغرافية الموضوع: DE

العلاقة: info:eu-repo/semantics/altIdentifier/issn/2330-9644; info:eu-repo/semantics/altIdentifier/issn/2168-6149; info:eu-repo/semantics/altIdentifier/issn/0003-9942; info:eu-repo/semantics/altIdentifier/issn/2168-6157; info:eu-repo/semantics/altIdentifier/issn/1538-3687; info:eu-repo/semantics/altIdentifier/pmid/pmid:24190229; info:eu-repo/semantics/altIdentifier/issn/0375-8540; https://pub.dzne.de/record/137239Test; https://pub.dzne.de/search?p=id:%22DZNE-2020-03561%22Test

الإتاحة: https://doi.org/10.1001/jamaneurol.2013.3682Test
https://pub.dzne.de/record/137239Test
https://pub.dzne.de/search?p=id:%22DZNE-2020-03561%22Test

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