Assessing whole-exome sequencing data from undiagnosed Brazilian patients to improve the diagnostic yield of inborn errors of immunity

被引:0
作者
Ferreira, Cristina Santos [1 ]
Francisco Junior, Ronaldo da Silva [1 ]
Gerber, Alexandra Lehmkuhl [1 ]
Guimaraes, Ana Paula de Campos [1 ]
Amendola, Flavia Anisio [2 ]
Pinto-Mariz, Fernanda [3 ]
de Souza, Monica Soares [4 ]
Miranda, Patricia Carvalho Batista [5 ]
de Vasconcelos, Zilton Farias Meira [6 ]
Goudouris, Ekaterini Simoes [3 ]
Vasconcelos, Ana Tereza Ribeiro [1 ]
机构
[1] MCTIC, Bioinformat Lab, Natl Lab Sci Computat LNCC, LABINFO, Ave Getulio Vargas 333, BR-25651075 Petropolis, RJ, Brazil
[2] Oswaldo Cruz Fdn FIOCRUZ, Allergy & Immunol Serv, Inst Women Children & Adolescents Hlth Fernandes F, Rio De Janeiro, RJ, Brazil
[3] Fed Univ Rio de Janeiro UFRJ, Allergy & Immunol Serv, Martagao Gesteira Inst Childcare & Pediat IPPMG, Rio De Janeiro, RJ, Brazil
[4] Fed Hosp State Employees HFSE, Hlth Minist, Rio De Janeiro, RJ, Brazil
[5] Lagoon Fed Hosp HFL, Hlth Minist, Rio De Janeiro, RJ, Brazil
[6] Oswaldo Cruz Fdn FIOCRUZ, Lab High Complex, Inst Women Children & Adolescents Hlth Fernandes F, Rio De Janeiro, RJ, Brazil
来源
BMC GENOMIC DATA | 2023年 / 24卷 / 01期
关键词
Whole exome sequencing; Single nucleotide variants; Monogenic disorder; Inborn errors of immunity; DROSOPHILA-MELANOGASTER; GENOMICS; PROGRAM;
D O I
10.1186/s12863-023-01137-2
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
ObjectivesInborn error of immunity (IEI) comprises a broad group of inherited immunological disorders that usually display an overlap in many clinical manifestations challenging their diagnosis. The identification of disease-causing variants from whole-exome sequencing (WES) data comprises the gold-standard approach to ascertain IEI diagnosis. The efforts to increase the availability of clinically relevant genomic data for these disorders constitute an important improvement in the study of rare genetic disorders. This work aims to make available WES data of Brazilian patients' suspicion of IEI without a genetic diagnosis. We foresee a broad use of this dataset by the scientific community in order to provide a more accurate diagnosis of IEI disorders.Data descriptionTwenty singleton unrelated patients treated at four different hospitals in the state of Rio de Janeiro, Brazil were enrolled in our study. Half of the patients were male with mean ages of 9 & PLUSMN; 3, while females were 12 & PLUSMN; 10 years old. The WES was performed in the Illumina NextSeq platform with at least 90% of sequenced bases with a minimum of 30 reads depth. Each sample had an average of 20,274 variants, comprising 116 classified as rare pathogenic or likely pathogenic according to American College of Medical Genetics and Genomics and the Association (ACMG) guidelines. The genotype-phenotype association was impaired by the lack of detailed clinical and laboratory information, besides the unavailability of molecular and functional studies which, comprise the limitations of this study. Overall, the access to clinical exome sequencing data is limited, challenging exploratory analyses and the understanding of genetic mechanisms underlying disorders. Therefore, by making these data available, we aim to increase the number of WES data from Brazilian samples despite contributing to the study of monogenic IEI-disorders.
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页数:5
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