المؤلفون: Wang, Zhiyang, Wang, Xinyu, Guo, Weiqi, Wang, Di, Hu, Jiangang, Zhang, Beibei, Qi, Jingjing, Tian, Mingxing, Bao, Yanqing, Li, Haihua, Wang, Shaohui

المصدر: Transboundary & Emerging Diseases; 2/16/2024, Vol. 2024, p1-9, 9p

مصطلحات موضوعية: GENOMICS, CEFTAZIDIME, BETA lactamases, ESCHERICHIA coli, WHOLE genome sequencing, POLYMYXIN B, MICROBIAL sensitivity tests

مصطلحات جغرافية: CHINA

المؤلفون: Karmacharya, Jayram¹ (AUTHOR), Shrestha, Prasansah¹ (AUTHOR), Han, So-Ra¹ (AUTHOR), Park, Hyun² (AUTHOR), Oh, Tae-Jin^1,3,4 (AUTHOR)

المصدر: International Journal of Microbiology. 8/25/2022, p1-12. 12p.

مصطلحات موضوعية: *WHOLE genome sequencing, *GENOMICS, *ARTHROBACTER, *MULTICOPPER oxidase, *MYCOBACTERIUM tuberculosis, *ESCHERICHIA coli, *GENOMES

المؤلفون: Shakeel, Muhammad, Irfan, Muhammad, Nisa, Zaib un, Farooq, Saba, Ain, Noor ul, Iqbal, Waseem, Kakar, Niamatullah, Jahan, Shah, Shahzad, Mohsin, Siddiqi, Saima, Khan, Ishtiaq Ahmad

المصدر: Transboundary & Emerging Diseases; Sep2022, Vol. 69 Issue 5, pe2418-e2430, 13p

مصطلحات موضوعية: GENOMICS, SARS-CoV-2, SEQUENCE analysis, WHOLE genome sequencing, COVID-19

مصطلحات جغرافية: PAKISTAN

المؤلفون: Zhu, Jie, Yang, Yi, Zhang, Xiaohui, Chen, Bixia, Liu, Guanxing, Bao, Endong

المصدر: Transboundary & Emerging Diseases; Sep2022, Vol. 69 Issue 5, p2952-2962, 11p

مصطلحات موضوعية: RUSSIAN history to 1533, GEESE, PARVOVIRUSES, AMINO acid analysis, WHOLE genome sequencing, DUCK plague, DUCKLINGS, WATERFOWL

مصطلحات جغرافية: CHINA

المؤلفون: Bhavi P. Modi, Alison M. Elliott, Wyeth W. Wasserman, Oriol Fornes, Phillip A. Richmond, Tamar V. Av-Shalom

المصدر: Human Mutation

مصطلحات موضوعية: Prioritization, Informatics, Population, rare disease, Genomics, Computational biology, Biology, 03 medical and health sciences, symbols.namesake, Rare Diseases, 0302 clinical medicine, Genetics, Humans, Genomic medicine, Computer Simulation, benchmarking, education, Gene, Genetics (clinical), 030304 developmental biology, Whole genome sequencing, 0303 health sciences, education.field_of_study, Whole Genome Sequencing, variant calling, Mechanism (biology), variant interpretation, 030305 genetics & heredity, High-Throughput Nucleotide Sequencing, simulation, Pathogenicity, 3. Good health, Phenotype, Mendelian inheritance, symbols, 030217 neurology & neurosurgery, Rare disease

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f174894a396e814a3a5608d03eb3dfa7Test
https://doi.org/10.1002/humu.24163Test

المؤلفون: Louise Christie, Thuong T. Ha, Patricia Sullivan, Thessa Kroes, Jozef Gecz, Mark A. Corbett, Tony Roscioli, Anna Hackett, Lisa Ewans, Cheryl Shoubridge, Marcel E. Dinger, Atma M. Ivancevic, Alison Gardner, Raman Kumar, Elizabeth E. Palmer, Sayaka Kayumi, Renee Carroll, Tracy Dudding-Byth, Mark J. Cowley, Marie Shaw, Michael Field, Charles E. Schwartz

المصدر: Human Mutation. 42:835-847

مصطلحات موضوعية: Whole genome sequencing, Regulation of gene expression, Genetics, 0303 health sciences, X-linked intellectual disability, 030305 genetics & heredity, Alternative splicing, Gene Expression, Genomics, Biology, medicine.disease, Phenotype, DNA sequencing, Pedigree, 03 medical and health sciences, Genes, X-Linked, Intellectual Disability, medicine, Humans, Trinucleotide repeat expansion, Gene, Genetics (clinical), 030304 developmental biology

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22e6bd121eb3728f96d6451cc3385d36Test
https://doi.org/10.1002/humu.24207Test

المؤلفون: John V. Pearson, Georgina E Hollway, Nicola Waddell, Felicity Newell, Aimee L Davidson, Lambros T. Koufariotis, Michael T. Parsons, Conrad Leonard, Amanda B. Spurdle

المصدر: Human Mutation. 42:530-536

مصطلحات موضوعية: Population, Computational biology, Biology, Germline, Cancer syndrome, Population genomics, 03 medical and health sciences, Gene Frequency, Neoplasms, Genetics, medicine, Humans, Genetic Testing, education, Gene, Allele frequency, Genetics (clinical), 030304 developmental biology, Whole genome sequencing, 0303 health sciences, education.field_of_study, Genome, Human, 030305 genetics & heredity, Genetic Variation, Genomics, medicine.disease, Germ Cells, Precision and recall

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2477344de3121b5defbb1f254cd036c1Test
https://doi.org/10.1002/humu.24183Test

المؤلفون: Julia Foreman, Simon Brent, Daniel Perrett, Andrew P. Bevan, Sarah E. Hunt, Fiona Cunningham, Matthew E. Hurles, Helen V. Firth

المساهمون: Foreman, Julia [0000-0003-4567-2479], Brent, Simon [0000-0001-9145-1541], Perrett, Daniel [0000-0002-5479-9386], Bevan, Andrew P [0000-0002-0656-9164], Hunt, Sarah E [0000-0002-8350-1235], Cunningham, Fiona [0000-0002-7445-2419], Hurles, Matthew E [0000-0002-2333-7015], Firth, Helen V [0000-0002-6410-0882], Apollo - University of Cambridge Repository

مصطلحات موضوعية: Interpretation (logic), Computer science, genotype phenotype correlation, variant interpretation, rare diseases, Computational biology, Genomics, Phenotype, Data type, genomic medicine, Matchmaker Exchange, whole-genome sequencing, Human Phenotype Ontology, Databases, Genetic, Genetics, DECIPHER, Humans, genetic disorders, whole-exome sequencing, Genetics (clinical), Software, Rare disease

وصف الملف: text/xml; application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a4765cb4a532010a0a92dce7cfb54c0Test

المؤلفون: Foreman, Julia, Brent, Simon, Perrett, Daniel, Bevan, Andrew P, Hunt, Sarah E, Cunningham, Fiona, Hurles, Matthew E, Firth, Helen V

مصطلحات موضوعية: Matchmaker Exchange, genetic disorders, genomic medicine, genotype phenotype correlation, rare diseases, variant interpretation, whole-exome sequencing, whole-genome sequencing, Databases, Genetic, Genomics, Humans, Phenotype, Software

وصف الملف: text/xml; application/pdf

العلاقة: https://www.repository.cam.ac.uk/handle/1810/334316Test

الإتاحة: https://doi.org/10.17863/CAM.81729Test
https://www.repository.cam.ac.uk/handle/1810/334316Test

المؤلفون: David N. Olivieri, Francisco Gambón-Deza

المصدر: Computational and Mathematical Methods in Medicine, Vol 2019 (2019)
Computational and Mathematical Methods in Medicine

مصطلحات موضوعية: Primates, Article Subject, Computer science, Gene prediction, 1206.01 Construcción de Algoritmos, lcsh:Computer applications to medicine. Medical informatics, Genome, General Biochemistry, Genetics and Molecular Biology, Business process discovery, 03 medical and health sciences, 0302 clinical medicine, Species Specificity, Databases, Genetic, Animals, Humans, Reinforcement learning, Ensembl, Genetic Association Studies, Phylogeny, Probability, 030304 developmental biology, Whole genome sequencing, 0303 health sciences, Whole Genome Sequencing, General Immunology and Microbiology, 2409 Genética, Shotgun sequencing, Applied Mathematics, Iterative learning control, Computational Biology, Exons, Genomics, General Medicine, Modeling and Simulation, lcsh:R858-859.7, Algorithm, Algorithms, Software, Research Article, 030215 immunology

وصف الملف: text/xhtml

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92a0fade3a59a8566012470a7715dd88Test
https://doi.org/10.1155/2019/3780245Test