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Tytuł:
Genome characterization of influenza A and B viruses in New South Wales, Australia, in 2019: A retrospective study using high-throughput whole genome sequencing.
Autorzy:
Wang X; School of Biomedical Sciences, Faculty of Medicine and Health University of New South Wales Sydney New South Wales Australia.; Virology Research Laboratory, Serology and Virology Division (SAViD), NSW Health Pathology Prince of Wales Hospital Sydney New South Wales Australia.
Kim KW; Virology Research Laboratory, Serology and Virology Division (SAViD), NSW Health Pathology Prince of Wales Hospital Sydney New South Wales Australia.; Discipline of Paediatrics and Child Health, School of Clinical Medicine, Faculty of Medicine and Health University of New South Wales Sydney New South Wales Australia.
Walker G; School of Biomedical Sciences, Faculty of Medicine and Health University of New South Wales Sydney New South Wales Australia.; Virology Research Laboratory, Serology and Virology Division (SAViD), NSW Health Pathology Prince of Wales Hospital Sydney New South Wales Australia.
Stelzer-Braid S; School of Biomedical Sciences, Faculty of Medicine and Health University of New South Wales Sydney New South Wales Australia.; Virology Research Laboratory, Serology and Virology Division (SAViD), NSW Health Pathology Prince of Wales Hospital Sydney New South Wales Australia.
Scotch M; Biodesign Center for Environmental Health Engineering, Biodesign Institute Arizona State University Phoenix Arizona USA.; College of Health Solutions Arizona State University Phoenix Arizona USA.; Kirby Institute University of New South Wales Sydney New South Wales Australia.
Rawlinson WD; School of Biomedical Sciences, Faculty of Medicine and Health University of New South Wales Sydney New South Wales Australia.; Virology Research Laboratory, Serology and Virology Division (SAViD), NSW Health Pathology Prince of Wales Hospital Sydney New South Wales Australia.
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Źródło:
Influenza and other respiratory viruses [Influenza Other Respir Viruses] 2024 Jan; Vol. 18 (1), pp. e13252.
Typ publikacji:
Journal Article
MeSH Terms:
Influenza, Human*
Herpesvirus 1, Cercopithecine*/genetics
Influenza Vaccines*
Humans ; Retrospective Studies ; Influenza A Virus, H3N2 Subtype/genetics ; New South Wales/epidemiology ; Phylogeny ; Hemagglutinin Glycoproteins, Influenza Virus/genetics ; Australia ; Seasons ; Whole Genome Sequencing
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Mutational analysis of severe acute respiratory syndrome coronavirus 2 in immunocompromised patients with persistent viral detection using whole genome sequencing.
Autorzy:
Chang E; Department of Infectious Diseases, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
Lee J; Department of Microbiology, Institute for Viral Diseases, Vaccine Innovation Center, Korea University College of Medicine, Seoul, Republic of Korea.
Kim JW; Division of Emerging Virus and Vector Research, Center for Emerging Virus Research, National Institute of Infectious Diseases, Korea Disease Control and Prevention Agency, Cheongju, Republic of Korea.
Seok JH; Department of Microbiology, Institute for Viral Diseases, Vaccine Innovation Center, Korea University College of Medicine, Seoul, Republic of Korea.
Bae JY; Department of Microbiology, Institute for Viral Diseases, Vaccine Innovation Center, Korea University College of Medicine, Seoul, Republic of Korea.
Kim J; Department of Microbiology, Institute for Viral Diseases, Vaccine Innovation Center, Korea University College of Medicine, Seoul, Republic of Korea.
Park H; Department of Microbiology, Institute for Viral Diseases, Vaccine Innovation Center, Korea University College of Medicine, Seoul, Republic of Korea.
Jang CY; Department of Infectious Diseases, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
Kang SW; Department of Infectious Diseases, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
Lim SY; Department of Infectious Diseases, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
Kim JY; Department of Infectious Diseases, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
Yang JS; Division of Emerging Virus and Vector Research, Center for Emerging Virus Research, National Institute of Infectious Diseases, Korea Disease Control and Prevention Agency, Cheongju, Republic of Korea.
Kim KC; Division of Emerging Virus and Vector Research, Center for Emerging Virus Research, National Institute of Infectious Diseases, Korea Disease Control and Prevention Agency, Cheongju, Republic of Korea.
Lee JY; Division of Emerging Virus and Vector Research, Center for Emerging Virus Research, National Institute of Infectious Diseases, Korea Disease Control and Prevention Agency, Cheongju, Republic of Korea.
Park MS; Department of Microbiology, Institute for Viral Diseases, Vaccine Innovation Center, Korea University College of Medicine, Seoul, Republic of Korea.
Kim SH; Department of Infectious Diseases, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
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Źródło:
Clinical and translational medicine [Clin Transl Med] 2023 Nov; Vol. 13 (11), pp. e1462.
Typ publikacji:
Letter; Research Support, Non-U.S. Gov't
MeSH Terms:
SARS-CoV-2*/genetics
COVID-19*/diagnosis
COVID-19*/genetics
Humans ; Whole Genome Sequencing ; Immunocompromised Host
Raport
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Use of whole genome sequencing to identify low-frequency mutations in SARS-CoV-2 patients treated with remdesivir.
Autorzy:
Nirmalarajah K; Sunnybrook Research Institute, Toronto, Ontario, Canada.; Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada.
Yim W; Sunnybrook Research Institute, Toronto, Ontario, Canada.
Aftanas P; Shared Hospital Laboratory, Toronto, Ontario, Canada.
Li AX; Sinai Health System, Toronto, Ontario, Canada.
Shigayeva A; Sinai Health System, Toronto, Ontario, Canada.
Yip L; Sunnybrook Research Institute, Toronto, Ontario, Canada.
Zhong Z; Sinai Health System, Toronto, Ontario, Canada.
McGeer AJ; Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada.; Sinai Health System, Toronto, Ontario, Canada.
Maguire F; Faculty of Computer Science, Dalhousie University, Halifax, Nova Scotia, Canada.; Department of Community Health & Epidemiology, Dalhousie University, Halifax, Nova Scotia, Canada.
Mubareka S; Sunnybrook Research Institute, Toronto, Ontario, Canada.; Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada.
Kozak R; Sunnybrook Research Institute, Toronto, Ontario, Canada.; Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada.
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Źródło:
Influenza and other respiratory viruses [Influenza Other Respir Viruses] 2023 Sep; Vol. 17 (9), pp. e13179.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
SARS-CoV-2*/genetics
COVID-19*
Humans ; COVID-19 Drug Treatment ; Mutation ; Whole Genome Sequencing
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Integrative genomic analysis reveals a conserved role for prolactin signalling in the regulation of adrenal function.
Autorzy:
Ruggiero C; Institut de Pharmacologie Moléculaire et Cellulaire CNRS UMR 7275, Valbonne, France.; Université Côte d'Azur, Valbonne, France.
Altieri B; Department of Internal Medicine I-Division of Endocrinology and Diabetes, University Hospital, University of Würzburg, Würzburg, Germany.
Arnold E; Instituto de Neurobiología, Universidad Nacional Autónoma de México (UNAM), Queretaro, Mexico.; CONACYT-Instituto de Neurobiología, Universidad Nacional Autónoma de México (UNAM), Queretaro, Mexico.
Siqueiros-Marquez L; Instituto de Neurobiología, Universidad Nacional Autónoma de México (UNAM), Queretaro, Mexico.
Doghman-Bouguerra M; Institut de Pharmacologie Moléculaire et Cellulaire CNRS UMR 7275, Valbonne, France.; Université Côte d'Azur, Valbonne, France.
Detomas M; Department of Internal Medicine I-Division of Endocrinology and Diabetes, University Hospital, University of Würzburg, Würzburg, Germany.
Durand N; Institut de Pharmacologie Moléculaire et Cellulaire CNRS UMR 7275, Valbonne, France.; Université Côte d'Azur, Valbonne, France.
Jarjat M; Institut de Pharmacologie Moléculaire et Cellulaire CNRS UMR 7275, Valbonne, France.; Université Côte d'Azur, Valbonne, France.
Kurlbaum M; Department of Internal Medicine I-Division of Endocrinology and Diabetes, University Hospital, University of Würzburg, Würzburg, Germany.; Central Laboratory, Core Unit Clinical Mass Spectrometry, University Hospital Würzburg, Würzburg, Germany.
Chatonnet F; Université de Rennes 1, Inserm, Établissement Français du Sang de Bretagne, Rennes, France.; Laboratoire d'Hématologie, Pôle de Biologie, Centre Hospitalier Universitaire, Rennes, France.
Deutschbein T; Department of Internal Medicine I-Division of Endocrinology and Diabetes, University Hospital, University of Würzburg, Würzburg, Germany.; Medicover Oldenburg MVZ, Oldenburg, Germany.
Clapp C; Instituto de Neurobiología, Universidad Nacional Autónoma de México (UNAM), Queretaro, Mexico.
Lalli E; Institut de Pharmacologie Moléculaire et Cellulaire CNRS UMR 7275, Valbonne, France.; Université Côte d'Azur, Valbonne, France.; Inserm, Valbonne, France.
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Źródło:
Clinical and translational medicine [Clin Transl Med] 2021 Nov; Vol. 11 (11), pp. e630.
Typ publikacji:
Letter; Research Support, Non-U.S. Gov't
MeSH Terms:
Adrenal Glands/*physiology
Prolactin/*metabolism
Whole Genome Sequencing/*statistics & numerical data
Adrenal Glands/metabolism ; Adrenal Glands/physiopathology ; Humans ; Prolactin/genetics ; Prolactin/pharmacology ; Whole Genome Sequencing/methods
Raport
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Single-cell RNA sequencing reveals the landscapes of human cord blood hematopoietic stem cell differentiation during ex vivo culture.
Autorzy:
Wen R; Department of Hematology, The Fifth Medical Center of Chinese PLA General Hospital, Beijing, PR China.; Department of Hematology, Central People's Hospital of Zhanjiang, Zhanjiang, PR China.; Academy of Military Medical Sciences, Academy of Military Sciences, Beijing, PR China.
Xu C; Department of Hematology, The Fifth Medical Center of Chinese PLA General Hospital, Beijing, PR China.; Academy of Military Medical Sciences, Academy of Military Sciences, Beijing, PR China.
Dong C; Department of Hematology, The Fifth Medical Center of Chinese PLA General Hospital, Beijing, PR China.; Academy of Military Medical Sciences, Academy of Military Sciences, Beijing, PR China.
Sheng H; Department of Hematology, The Fifth Medical Center of Chinese PLA General Hospital, Beijing, PR China.
Zhao L; Department of Hematology, The Fifth Medical Center of Chinese PLA General Hospital, Beijing, PR China.
Yang Y; Department of Hematology, The Fifth Medical Center of Chinese PLA General Hospital, Beijing, PR China.
Zhang A; Department of Hematology, The Fifth Medical Center of Chinese PLA General Hospital, Beijing, PR China.
Wang S; Department of Hematology, The Fifth Medical Center of Chinese PLA General Hospital, Beijing, PR China.
Wang L; Department of Obstetrical, The Fifth Medical Center of Chinese PLA General Hospital, Beijing, PR China.
Ju Y; Department of Obstetrical, The Fifth Medical Center of Chinese PLA General Hospital, Beijing, PR China.
Liu Y; Department of Obstetrical, The Fifth Medical Center of Chinese PLA General Hospital, Beijing, PR China.
Duan L; Department of Neurosurgery, The Fifth Medical Center of Chinese PLA General Hospital, Beijing, PR China.
Hu L; Department of Hematology, The Fifth Medical Center of Chinese PLA General Hospital, Beijing, PR China.
Chen H; Department of Hematology, The Fifth Medical Center of Chinese PLA General Hospital, Beijing, PR China.
Yang Z; Department of Hematology, Central People's Hospital of Zhanjiang, Zhanjiang, PR China.
Zhang B; Department of Hematology, The Fifth Medical Center of Chinese PLA General Hospital, Beijing, PR China.
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Źródło:
Clinical and translational medicine [Clin Transl Med] 2021 Nov; Vol. 11 (11), pp. e616.
Typ publikacji:
Letter; Research Support, Non-U.S. Gov't
MeSH Terms:
Fetal Blood/*cytology
RNA/*analysis
Whole Genome Sequencing/*statistics & numerical data
Fetal Blood/metabolism ; Hematopoietic Stem Cells/cytology ; Hematopoietic Stem Cells/physiology ; Humans ; RNA/blood ; Single-Cell Analysis/methods ; Single-Cell Analysis/statistics & numerical data ; Whole Genome Sequencing/methods
Raport
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Colorectal mucinous adenocarcinoma indicates a meaningful subtype: A whole genome sequencing study.
Autorzy:
Xu Y; The First Affiliated Hospital, Cancer Research Institute, Hengyang Medical School, University of South China, Hengyang, P. R. China.; The First Affiliated Hospital, Institute of Clinical Medicine, Hengyang Medical School, University of South China, Hengyang, P. R. China.
Chen X; The First Affiliated Hospital, Cancer Research Institute, Hengyang Medical School, University of South China, Hengyang, P. R. China.; The First Affiliated Hospital, Institute of Clinical Medicine, Hengyang Medical School, University of South China, Hengyang, P. R. China.
Chen Y; Institute of Molecular Precision Medicine and Hunan Key Laboratory of Molecular Precision Medicine, Xiangya Hospital, Central South University, Changsha, P. R. China.
Wu X; The First Affiliated Hospital, Cancer Research Institute, Hengyang Medical School, University of South China, Hengyang, P. R. China.; The First Affiliated Hospital, Department of Gastrointestinal Surgery, Hengyang Medical School, University of South China, Hengyang, P. R. China.
Fang Q; The First Affiliated Hospital, Cancer Research Institute, Hengyang Medical School, University of South China, Hengyang, P. R. China.; The First Affiliated Hospital, Department of Gastrointestinal Surgery, Hengyang Medical School, University of South China, Hengyang, P. R. China.
Tan X; The First Affiliated Hospital, Cancer Research Institute, Hengyang Medical School, University of South China, Hengyang, P. R. China.
Li S; The First Affiliated Hospital, Cancer Research Institute, Hengyang Medical School, University of South China, Hengyang, P. R. China.; The First Affiliated Hospital, Department of Gastrointestinal Surgery, Hengyang Medical School, University of South China, Hengyang, P. R. China.
Huang Q; The First Affiliated Hospital, Department of Gastrointestinal Surgery, Hengyang Medical School, University of South China, Hengyang, P. R. China.
Zu X; The First Affiliated Hospital, Cancer Research Institute, Hengyang Medical School, University of South China, Hengyang, P. R. China.; The First Affiliated Hospital, Institute of Clinical Medicine, Hengyang Medical School, University of South China, Hengyang, P. R. China.
Fu K; Institute of Molecular Precision Medicine and Hunan Key Laboratory of Molecular Precision Medicine, Xiangya Hospital, Central South University, Changsha, P. R. China.
Xiao S; The First Affiliated Hospital, Cancer Research Institute, Hengyang Medical School, University of South China, Hengyang, P. R. China.; The First Affiliated Hospital, Institute of Clinical Medicine, Hengyang Medical School, University of South China, Hengyang, P. R. China.; The First Affiliated Hospital, Department of Gastrointestinal Surgery, Hengyang Medical School, University of South China, Hengyang, P. R. China.
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Źródło:
Clinical and translational medicine [Clin Transl Med] 2023 Apr; Vol. 13 (4), pp. e1246.
Typ publikacji:
Letter; Research Support, Non-U.S. Gov't
MeSH Terms:
Colorectal Neoplasms*/genetics
Colorectal Neoplasms*/pathology
Adenocarcinoma, Mucinous*/diagnosis
Adenocarcinoma, Mucinous*/genetics
Adenocarcinoma, Mucinous*/pathology
Humans ; Whole Genome Sequencing
Raport
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Detection of candidate polymorphisms around the QTL for fat area ratio to rib eye area on BTA7 using whole-genome resequencing in Japanese Black cattle.
Autorzy:
Sasazaki S; Laboratory of Animal Breeding and Genetics, Graduate School of Agricultural Science, Kobe University, Kobe, Japan.
Kawaguchi F; Laboratory of Animal Breeding and Genetics, Graduate School of Agricultural Science, Kobe University, Kobe, Japan.
Nakajima A; Laboratory of Animal Breeding and Genetics, Graduate School of Agricultural Science, Kobe University, Kobe, Japan.
Yamamoto R; Laboratory of Animal Breeding and Genetics, Graduate School of Agricultural Science, Kobe University, Kobe, Japan.
Akiyama T; Hyogo Prefectural Technology Center for Agriculture, Hokubu Agricultural Technology Institute, Asago, Japan.
Kohama N; Hyogo Prefectural Technology Center for Agriculture, Hokubu Agricultural Technology Institute, Asago, Japan.
Yoshida E; Hyogo Prefectural Technology Center for Agriculture, Forestry and Fisheries, Kasai, Japan.
Kobayashi E; Division of Animal Breeding and Reproduction Research, Institute of Livestock and Grassland Science, National Agriculture and Food Research Organization, Tsukuba, Japan.
Honda T; Food Resources Education & Research Center, Kobe University, Kasai, Japan.
Oyama K; Food Resources Education & Research Center, Kobe University, Kasai, Japan.
Mannen H; Laboratory of Animal Breeding and Genetics, Graduate School of Agricultural Science, Kobe University, Kobe, Japan.
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Źródło:
Animal science journal = Nihon chikusan Gakkaiho [Anim Sci J] 2020 Jan-Dec; Vol. 91 (1), pp. e13335.
Typ publikacji:
Journal Article
MeSH Terms:
Polymorphism, Single Nucleotide*
Cattle/*genetics
Quantitative Trait Loci/*genetics
Whole Genome Sequencing/*veterinary
Animals ; Genetic Association Studies/methods ; Genome-Wide Association Study/veterinary ; Japan ; Whole Genome Sequencing/methods
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
A pilot study of assessing whole genome sequencing in newborn screening in unselected children in China.
Autorzy:
Jian M; BGI-Shenzhen, Shenzhen, China.; China National GeneBank, BGI-Shenzhen, Shenzhen, China.; Department of Biology, University of Copenhagen, Copenhagen, Denmark.
Wang X; BGI-Qingdao, BGI-Shenzhen, Qingdao, China.
Sui Y; Maternal and Child Health and Family Planning Service Center of Huangdao District, Qingdao, China.
Fang M; BGI-Shenzhen, Shenzhen, China.; China National GeneBank, BGI-Shenzhen, Shenzhen, China.
Feng C; BGI-Shenzhen, Shenzhen, China.; China National GeneBank, BGI-Shenzhen, Shenzhen, China.
Huang Y; BGI-Qingdao, BGI-Shenzhen, Qingdao, China.
Liu C; Maternal and Child Health and Family Planning Service Center of Huangdao District, Qingdao, China.
Guo R; BGI-Shenzhen, Shenzhen, China.; China National GeneBank, BGI-Shenzhen, Shenzhen, China.
Guan Y; BGI-Qingdao, BGI-Shenzhen, Qingdao, China.
Gao Y; Maternal and Child Health and Family Planning Service Center of Huangdao District, Qingdao, China.
Wang Z; BGI-Qingdao, BGI-Shenzhen, Qingdao, China.
Li S; Traditional Chinese Medical Hospital of Huangdao District, Qingdao, China.
Cheng B; BGI-Shenzhen, Shenzhen, China.; China National GeneBank, BGI-Shenzhen, Shenzhen, China.
Sun L; BGI-Qingdao, BGI-Shenzhen, Qingdao, China.
Cui F; The Affiliated Hospital of Qingdao University, Qingdao, China.
Guo J; BGI-Shenzhen, Shenzhen, China.; China National GeneBank, BGI-Shenzhen, Shenzhen, China.
Zhan Y; Qindgao West Coast New Area Central Hospital, Qingdao, China.
Zhang G; BGI-Shenzhen, Shenzhen, China.; China National GeneBank, BGI-Shenzhen, Shenzhen, China.
Zheng L; Traditional Chinese Medical Hospital of Huangdao District, Qingdao, China.
Su F; BGI-Shenzhen, Shenzhen, China.; China National GeneBank, BGI-Shenzhen, Shenzhen, China.
Xue W; The Affiliated Hospital of Qingdao University, Qingdao, China.
Qian P; BGI-Shenzhen, Shenzhen, China.; China National GeneBank, BGI-Shenzhen, Shenzhen, China.
Gao S; Qindgao West Coast New Area Central Hospital, Qingdao, China.
Chen J; BGI-Shenzhen, Shenzhen, China.; China National GeneBank, BGI-Shenzhen, Shenzhen, China.
Guan L; BGI-Shenzhen, Shenzhen, China.; China National GeneBank, BGI-Shenzhen, Shenzhen, China.
Lu H; BGI-Shenzhen, Shenzhen, China.; China National GeneBank, BGI-Shenzhen, Shenzhen, China.; Guangdong Provincial Key Laboratory of Genome Read and Write, BGI-Shenzhen, Shenzhen, China.
Kristiansen K; Department of Biology, University of Copenhagen, Copenhagen, Denmark.
Jin X; BGI-Shenzhen, Shenzhen, China.; China National GeneBank, BGI-Shenzhen, Shenzhen, China.
Chen F; BGI-Shenzhen, Shenzhen, China.; China National GeneBank, BGI-Shenzhen, Shenzhen, China.
Zhao Y; Medical Career Development Center, Huangdao District, Qingdao, China.
Hammarström L; BGI-Shenzhen, Shenzhen, China.; China National GeneBank, BGI-Shenzhen, Shenzhen, China.
Jiang X; Maternal and Child Health and Family Planning Service Center of Huangdao District, Qingdao, China.
Liu J; BGI-Shenzhen, Shenzhen, China.; China National GeneBank, BGI-Shenzhen, Shenzhen, China.; BGI-Qingdao, BGI-Shenzhen, Qingdao, China.
Gao Y; BGI-Shenzhen, Shenzhen, China.; China National GeneBank, BGI-Shenzhen, Shenzhen, China.; Shenzhen Engineering Laboratory for Birth Defects Screening, Shenzhen, China.
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Źródło:
Clinical and translational medicine [Clin Transl Med] 2022 Jun; Vol. 12 (6), pp. e843.
Typ publikacji:
Letter; Research Support, Non-U.S. Gov't
MeSH Terms:
Neonatal Screening*
Child ; China/epidemiology ; Humans ; Infant, Newborn ; Pilot Projects ; Sequence Analysis, DNA ; Whole Genome Sequencing
Raport
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Identification of clinically actionable secondary genetic variants from whole-genome sequencing in a large-scale Chinese population.
Autorzy:
Cong PK; Diseases & Population (DaP) Geninfo Lab, School of Life Sciences, Westlake University, Hangzhou, Zhejiang, China.; Westlake Laboratory of Life Sciences and Biomedicine, Hangzhou, Zhejiang, China.; Institute of Basic Medical Sciences, Westlake Institute for Advanced Study, Hangzhou, Zhejiang, China.
Khederzadeh S; Diseases & Population (DaP) Geninfo Lab, School of Life Sciences, Westlake University, Hangzhou, Zhejiang, China.; Westlake Laboratory of Life Sciences and Biomedicine, Hangzhou, Zhejiang, China.; Institute of Basic Medical Sciences, Westlake Institute for Advanced Study, Hangzhou, Zhejiang, China.
Yuan CD; Department of Dermatology, Hangzhou Hospital of Traditional Chinese Medicine, Hangzhou, Zhejiang, China.
Ma RJ; Diseases & Population (DaP) Geninfo Lab, School of Life Sciences, Westlake University, Hangzhou, Zhejiang, China.
Zhang YY; Diseases & Population (DaP) Geninfo Lab, School of Life Sciences, Westlake University, Hangzhou, Zhejiang, China.
Liu JQ; Clinical Genome Center, KingMed Diagnostics, Co. Ltd., Guangzhou, Guangdong, China.
Yu SH; Clinical Genome Center, KingMed Diagnostics, Co. Ltd., Guangzhou, Guangdong, China.
Xu L; WBBC Shandong Center, Binzhou Medical University, Yantai, Shandong, China.
Gao JH; WBBC Jiangxi Center, Jiangxi Medical College, Shangrao, Jiangxi, China.
Pan HX; National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, Hunan, China.; Department of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Li JC; National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, Hunan, China.; Department of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Xie SY; WBBC Shandong Center, Binzhou Medical University, Yantai, Shandong, China.
Liu KQ; WBBC Jiangxi Center, Jiangxi Medical College, Shangrao, Jiangxi, China.
Tang BS; National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, Hunan, China.; Department of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Zheng HF; Diseases & Population (DaP) Geninfo Lab, School of Life Sciences, Westlake University, Hangzhou, Zhejiang, China.; Westlake Laboratory of Life Sciences and Biomedicine, Hangzhou, Zhejiang, China.; Institute of Basic Medical Sciences, Westlake Institute for Advanced Study, Hangzhou, Zhejiang, China.
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Źródło:
Clinical and translational medicine [Clin Transl Med] 2022 May; Vol. 12 (5), pp. e866.
Typ publikacji:
Letter; Research Support, Non-U.S. Gov't
MeSH Terms:
Asian People*/genetics
China ; Humans ; Whole Genome Sequencing
Raport
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Whole-genome sequencing and antigenic analysis of the first equine influenza virus identified in Turkey.
Autorzy:
Gahan J; Virology Unit, Irish Equine Centre, Naas, Ireland.
Garvey M; Virology Unit, Irish Equine Centre, Naas, Ireland.
Gildea S; Virology Unit, Irish Equine Centre, Naas, Ireland.
Gür E; Head of Equine Health and Veterinary Services Department, Jockey Club of Turkey, Istanbul, Turkey.
Kagankaya A; Department of Surgery, Ankara University Faculty of Veterinary Medicine, Ankara, Turkey.
Cullinane A; Virology Unit, Irish Equine Centre, Naas, Ireland.
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Źródło:
Influenza and other respiratory viruses [Influenza Other Respir Viruses] 2018 May; Vol. 12 (3), pp. 374-382. Date of Electronic Publication: 2018 Feb 08.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Whole Genome Sequencing*
Disease Outbreaks/*veterinary
Horses/*virology
Influenza A Virus, H3N8 Subtype/*genetics
Orthomyxoviridae Infections/*veterinary
Animals ; Antigens, Viral/genetics ; Genetic Variation ; Influenza A Virus, H3N8 Subtype/isolation & purification ; Orthomyxoviridae Infections/diagnosis ; Orthomyxoviridae Infections/virology ; Phylogeny ; Real-Time Polymerase Chain Reaction ; Turkey ; Viral Nonstructural Proteins/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Leveraging multiple approaches for the detection of pathogenic deep intronic variants in developmental and epileptic encephalopathies: A case report
Autorzy:
Denis M. Nyaga
Michael S. Hildebrand
Guillem deValles‐Ibáñez
Ngaire F. Keenan
Zimeng Ye
Christy W. LaFlamme
Heather C. Mefford
Mark F. Bennett
Melanie Bahlo
Lynette G. Sadleir
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Temat:
genetic testing
PAFAH1B1
SCN1A
SNP arrays
structural variants
whole‐genome sequencing
Neurology. Diseases of the nervous system
RC346-429
Źródło:
Epilepsia Open, Vol 9, Iss 2, Pp 758-764 (2024)
Opis pliku:
electronic resource
Relacje:
https://doaj.org/toc/2470-9239
Dostęp URL:
https://doaj.org/article/3103487ddc324b14b1add1c9184bb83f  Link otwiera się w nowym oknie
Czasopismo naukowe
Szczegóły
Tytuł:
Comparative genomics and fermentation flavor characterization of five selected lactic acid bacteria provide predictions for flavor biosynthesis metabolic pathways in fermented muskmelon puree
Autorzy:
Lin Yuan
Meilun Li
Xinxing Xu
Xun Shi
Guogang Chen
Fei Lao
Jihong Wu
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Temat:
comparative genomic analysis
flavor biosynthesis metabolism
lactic acid bacteria
muskmelon
whole‐genome sequencing
Nutrition. Foods and food supply
TX341-641
Food processing and manufacture
TP368-456
Źródło:
Food Frontiers, Vol 5, Iss 2, Pp 508-521 (2024)
Opis pliku:
electronic resource
Relacje:
https://doaj.org/toc/2643-8429
Dostęp URL:
https://doaj.org/article/0da8b33b10a04e65b441d3467eb6086a  Link otwiera się w nowym oknie
Czasopismo naukowe
Szczegóły
Tytuł:
Population assignment from genotype likelihoods for low‐coverage whole‐genome sequencing data
Autorzy:
Matthew G. DeSaix
Marina D. Rodriguez
Kristen C. Ruegg
Eric C. Anderson
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Temat:
Fisher information
genetic stock identification
genotype likelihoods
low‐coverage whole‐genome sequencing
next‐generation sequencing
population assignment
Ecology
QH540-549.5
Evolution
QH359-425
Źródło:
Methods in Ecology and Evolution, Vol 15, Iss 3, Pp 493-510 (2024)
Opis pliku:
electronic resource
Relacje:
https://doaj.org/toc/2041-210X
Dostęp URL:
https://doaj.org/article/1f897a8e79d64b82aba5cf6c62e495e8  Link otwiera się w nowym oknie
Czasopismo naukowe
Szczegóły
Tytuł:
Whole-genome sequencing identifies novel candidate pathogenic variants associated with left ventricular non-compaction in a three-generation family.
Autorzy:
Zhang Z; Department of Cardiology, Zhuhai People's Hospital (Zhuhai Hospital Affiliated with Jinan University), Zhuhai, Guangdong, P. R. China.
Li S; Shenzhen Byoryn Technology Co., Ltd, Shenzhen, Guangdong, P. R. China.
Wang K; Department of Cardiology, Zhuhai People's Hospital (Zhuhai Hospital Affiliated with Jinan University), Zhuhai, Guangdong, P. R. China.
Zhao Z; Shenzhen Byoryn Technology Co., Ltd, Shenzhen, Guangdong, P. R. China.
Zhang H; Department of Ultrasonography, Zhuhai People's Hospital (Zhuhai Hospital Affiliated with Jinan University), Zhuhai, Guangdong, P. R. China.
Li S; Shenzhen Research Institute, City University of Hong Kong, Shenzhen, Guangdong, P. R. China.
Jiang X; Department of Cardiology, Zhuhai People's Hospital (Zhuhai Hospital Affiliated with Jinan University), Zhuhai, Guangdong, P. R. China.
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Źródło:
Clinical and translational medicine [Clin Transl Med] 2021 Aug; Vol. 11 (8), pp. e501.
Typ publikacji:
Letter; Research Support, Non-U.S. Gov't
MeSH Terms:
Heart Defects, Congenital/*diagnostic imaging
Heart Defects, Congenital/*genetics
Whole Genome Sequencing/*methods
Child ; China ; Echocardiography/methods ; Female ; Heart Ventricles/diagnostic imaging ; Humans ; Male ; Middle Aged
SCR Disease Name:
Noncompaction of Left Ventricular Myocardium with Congenital Heart Defects
Raport
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Risk of symptomatic COVID-19 due to aircraft transmission: a retrospective cohort study of contact-traced flights during England's containment phase.
Autorzy:
Blomquist PB; UK Field Epidemiology Training Programme, Public Health England, London, United Kingdom.; North West Field Services, National Infection Service, Public Health England, Liverpool, United Kingdom.
Bolt H; South East and London Field Services, National Infection Service, Public Health England, London, United Kingdom.
Packer S; South West Field Services, National Infection Service, Public Health England, Bristol, United Kingdom.
Schaefer U; Core Bioinformatics Group, Data and Analytical Sciences, National Infection Service, Public Health England, London, United Kingdom.
Platt S; National Infection Service, Public Health England, London, United Kingdom.
Dabrera G; National Infection Service, Public Health England, London, United Kingdom.
Gobin M; South West Field Services, National Infection Service, Public Health England, Bristol, United Kingdom.
Oliver I; National Infection Service, Public Health England, London, United Kingdom.
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Źródło:
Influenza and other respiratory viruses [Influenza Other Respir Viruses] 2021 May; Vol. 15 (3), pp. 336-344. Date of Electronic Publication: 2021 Mar 01.
Typ publikacji:
Journal Article
MeSH Terms:
Air Travel*
Contact Tracing*
SARS-CoV-2*
COVID-19/*transmission
Adult ; COVID-19/etiology ; COVID-19/prevention & control ; Female ; Humans ; Male ; Middle Aged ; Physical Distancing ; Retrospective Studies ; Risk Factors ; Whole Genome Sequencing
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Precision medicine using whole genome sequencing identifies a novel dystrophin (DMD) variant for X‐linked muscular dystrophy in a cat
Autorzy:
G. Diane Shelton
Fabrizio Tucciarone
Ling T. Guo
Lyndon M. Coghill
Leslie A. Lyons
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Temat:
animal models
Felis catus
precision medicine
whole genome sequencing
Veterinary medicine
SF600-1100
Źródło:
Journal of Veterinary Internal Medicine, Vol 38, Iss 1, Pp 135-144 (2024)
Opis pliku:
electronic resource
Relacje:
https://doaj.org/toc/0891-6640; https://doaj.org/toc/1939-1676
Dostęp URL:
https://doaj.org/article/09b39a86188e450caec7328ebde389b7  Link otwiera się w nowym oknie
Czasopismo naukowe
Szczegóły
Tytuł:
Translational practice of fluorescence in situ hybridisation to identify neuroblastic tumours with TERT rearrangements
Autorzy:
Yongbo Yu
Meng Zhang
Xingfeng Yao
Xiaoxing Guan
Chao Jia
Ping Chu
Ruqian Zhang
Yeran Yang
Yaqiong Jin
Huanmin Wang
Xin Ni
Lejian He
Yongli Guo
Pokaż więcej
Temat:
neuroblastic tumour
neuroblastoma
TERT rearrangement
fluorescence in situ hybridisation
whole‐genome sequencing
Pathology
RB1-214
Źródło:
The Journal of Pathology: Clinical Research, Vol 9, Iss 6, Pp 475-487 (2023)
Opis pliku:
electronic resource
Relacje:
https://doaj.org/toc/2056-4538
Dostęp URL:
https://doaj.org/article/83195e5b5c664b0cae1557c544d4949e  Link otwiera się w nowym oknie
Czasopismo naukowe
Szczegóły
Tytuł:
The spotted parrotfish genome provides insights into the evolution of a coral reef dietary specialist (Teleostei: Labridae: Scarini: Cetoscarus ocellatus)
Autorzy:
Yi‐Kai Tea
Yulu Zhou
Kyle M. Ewart
Guo Cheng
Kazuhiko Kawasaki
Joseph D. DiBattista
Simon Y. W. Ho
Nathan Lo
Shaohua Fan
Pokaż więcej
Temat:
adaptation to dietary toxins
coral reef fish
Labridae
Scarini
whole‐genome sequencing
Ecology
QH540-549.5
Źródło:
Ecology and Evolution, Vol 14, Iss 3, Pp n/a-n/a (2024)
Opis pliku:
electronic resource
Relacje:
https://doaj.org/toc/2045-7758
Dostęp URL:
https://doaj.org/article/456d73ee782340be9fcc632bd1793ab6  Link otwiera się w nowym oknie
Czasopismo naukowe
Szczegóły
Tytuł:
Genomic evidence for domestication selection in three hatchery populations of Chinook salmon, Oncorhynchus tshawytscha
Autorzy:
Natasha S. Howe
Matthew C. Hale
Charles D. Waters
Sara M. Schaal
Kyle R. Shedd
Wesley A. Larson
Pokaż więcej
Temat:
domestication selection
hatchery
low‐coverage whole‐genome sequencing
rapid adaptation
salmon
Southeast Alaska
Evolution
QH359-425
Źródło:
Evolutionary Applications, Vol 17, Iss 2, Pp n/a-n/a (2024)
Opis pliku:
electronic resource
Relacje:
https://doaj.org/toc/1752-4571
Dostęp URL:
https://doaj.org/article/d8bf026bbb514f8bafe74722ddac7119  Link otwiera się w nowym oknie
Czasopismo naukowe
Szczegóły
Wyświetlanie 1-20 z 568

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