Cargando…

Preliminary evaluation of exome sequencing to identify genetic markers of susceptibility to tuberculosis disease

BACKGROUND: Recent studies have shown that certain human genetic polymorphisms could be associated with susceptibility to tuberculosis (TB) infection and disease. Advances in next generation sequencing include the ability to rapidly sequence the entire human exome. These new technologies can be expl...

Descripción completa

Detalles Bibliográficos
Autores principales:	Duncan, Carla, Jamieson, Frances, Mehaffy, Carolina
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2015
Materias:	Short Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4672511/ https://www.ncbi.nlm.nih.gov/pubmed/26643661 http://dx.doi.org/10.1186/s13104-015-1740-5

Ejemplares similares

Whole transcriptomic and proteomic analyses of an isogenic M. tuberculosis clinical strain with a naturally occurring 15 Kb genomic deletion
por: Duncan, Carla, et al.
Publicado: (2017)

Whole exome sequencing to identify genetic markers for trastuzumab‐induced cardiotoxicity
por: Udagawa, Chihiro, et al.
Publicado: (2018)

The GENCODE exome: sequencing the complete human exome
por: Coffey, Alison J, et al.
Publicado: (2011)

Exome Sequencing Identifies Susceptibility Loci for Sarcoidosis Prognosis
por: Lahtela, Elisa, et al.
Publicado: (2019)

Marked Microevolution of a Unique Mycobacterium tuberculosis Strain in 17 Years of Ongoing Transmission in a High Risk Population
por: Mehaffy, Carolina, et al.
Publicado: (2014)

PNKP Mutations Identified by Whole-Exome Sequencing in a Norwegian Patient with Sporadic Ataxia and Edema
por: Tzoulis, C., et al.
Publicado: (2016)

Whole exome sequencing identifies a mutation in thrombomodulin as the genetic cause of a suspected platelet disorder in a family with normal platelet function
por: Maclachlan, Annabel, et al.
Publicado: (2017)

Genetic Factors in Antiphospholipid Syndrome: Preliminary Experience with Whole Exome Sequencing
por: Barinotti, Alice, et al.
Publicado: (2020)

Candidate genes and sequence variants for susceptibility to mycobacterial infection identified by whole-exome sequencing
por: Varzari, Alexander, et al.
Publicado: (2022)

Whole-exome sequencing identified a novel mutation of MLH1 in an extended family with lynch syndrome
por: Ghaedi, Hamid, et al.
Publicado: (2019)

Twenty-one new sequence markers for population genetics, species delimitation and phylogenetics in wall lizards (Podarcis spp.)
por: Pereira, Carolina, et al.
Publicado: (2013)

Novel genetic susceptibility loci identified by family based whole exome sequencing in Han Chinese schizophrenia patients
por: Li, Mo, et al.
Publicado: (2020)

Identification of HLA-DQA1 as a Susceptibility Gene for Spinal Tuberculosis by Exome Sequencing
por: Shen, Jian, et al.
Publicado: (2018)

Whole-exome sequencing reveals insights into genetic susceptibility to Congenital Zika Syndrome
por: Borda, Victor, et al.
Publicado: (2021)

The use of whole-exome sequencing to disentangle complex phenotypes
por: Williams, Hywel J, et al.
Publicado: (2016)

Exome sequencing of three cases of familial exceptional longevity
por: Cash, Timothy P, et al.
Publicado: (2014)

Development of Genetic Markers in Eucalyptus Species by Target Enrichment and Exome Sequencing
por: Dasgupta, Modhumita Ghosh, et al.
Publicado: (2015)

Whole-exome sequencing analysis identifies novel variants associated with Kawasaki disease susceptibility
por: Zhang, Xing, et al.
Publicado: (2023)

Common Variable Immunodeficiency with Genetic Defects Identified by Whole Exome Sequencing
por: Li, Ran, et al.
Publicado: (2018)

Whole-Exome Sequencing for Identifying Genetic Causes of Intellectual Developmental Disorders
por: Guo, Yu-Xiong, et al.
Publicado: (2021)

An exome sequencing strategy to diagnose lethal autosomal recessive disorders
por: Ellard, Sian, et al.
Publicado: (2015)

Rapid exome sequencing: revolutionises the management of acutely unwell neonates
por: Williamson, Sarah L, et al.
Publicado: (2021)

Gene discovery for complex diseases using exomic sequencing: identifying pancreatic cancer susceptibility genes
por: Klein, Alison P
Publicado: (2010)

Early exploration of two candidate breast cancer susceptibility genes identified by whole-exome sequencing
por: Blanc, R, et al.
Publicado: (2012)

Whole-exome sequencing identifies susceptibility genes and pathways for idiopathic pulmonary fibrosis in the Chinese population
por: Fang, Chuling, et al.
Publicado: (2021)

Exome sequencing identified rare recurrent copy number variants and hereditary breast cancer susceptibility
por: Kumpula, Timo A., et al.
Publicado: (2023)

Genetically diverse mice are novel and valuable models of age-associated susceptibility to Mycobacterium tuberculosis
por: Harrison, David E, et al.
Publicado: (2014)

Whole-exome sequencing, without prior linkage, identifies a mutation in LAMB3 as a cause of dominant hypoplastic amelogenesis imperfecta
por: Poulter, James A, et al.
Publicado: (2014)

Utility of clinical exome sequencing in a complex Emirati pediatric cohort
por: Mahfouz, Nour Abu, et al.
Publicado: (2020)

Genetic Mapping and Exome Sequencing Identify Variants Associated with Five Novel Diseases
por: Puffenberger, Erik G., et al.
Publicado: (2012)

Whole Exome Sequencing Identifies Novel Genetic Alterations in Patients with Pheochromocytoma/Paraganglioma
por: Seo, Soo Hyun, et al.
Publicado: (2020)

Whole exome sequencing identifies novel inherited genetic variants in tetralogy of Fallot
por: Pan, Yu, et al.
Publicado: (2022)

Whole-exome sequencing to identify somatic mutations in peritoneal metastatic gastric adenocarcinoma: A preliminary study
por: Liu, Hao, et al.
Publicado: (2016)

Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing
por: Sifrim, Alejandro, et al.
Publicado: (2016)

Identifying genetic markers associated with susceptibility to cardiovascular diseases
por: Shukla, Hitesh, et al.
Publicado: (2018)

Whole exome sequencing identifies novel candidate genes that modify chronic obstructive pulmonary disease susceptibility
por: Bruse, Shannon, et al.
Publicado: (2016)

Exome Sequencing Identifies a Novel Gene, WNK1, for Susceptibility to Pelvic Organ Prolapse (POP)
por: Rao, Shuquan, et al.
Publicado: (2015)

Whole-exome sequencing in a Japanese multiplex family identifies new susceptibility genes for intracranial aneurysms
por: Maegawa, Tatsuya, et al.
Publicado: (2022)

Extracellular Vesicles in Mycobacteria and Tuberculosis
por: Mehaffy, Carolina, et al.
Publicado: (2022)

Longitudinal exome-wide association study to identify genetic susceptibility loci for hypertension in a Japanese population
por: Yasukochi, Yoshiki, et al.
Publicado: (2017)

Cannot write session to /tmp/vufind_sessions/sess_h1dpkigchnjtm0c94c9lqlps6t