Are we ready for whole population genomic sequencing of asymptomatic newborns?

Are we ready for whole population genomic sequencing of asymptomatic newborns?

The introduction of genomic sequencing technologies into routine newborn screening programs in some form is not only inevitable but also already occurring in some settings. The question is therefore not "if" but "when and how" genomic newborn screening (GNBS) should be implemente...

Descripció completa

Dades bibliogràfiques
Autors principals:	Vears, DF, Savulescu, J, Christodoulou, J, Wall, M, Newson, AJ
Format:	Journal article
Idioma:	English
Publicat:	Dove Press 2023

Ítems similars

Genomic intensive care: should we perform genome testing in critically ill newborns?
per: Wilkinson, D, et al.
Publicat: (2015)

Australian public perspectives on genomic newborn screening: which conditions should be included?
per: Lynch, F, et al.
Publicat: (2024)

Paving the path for implementation of clinical genomic sequencing globally: Are we ready?
per: Marshall, DA, et al.
Publicat: (2024)

Whole-Genome Sequences and Classification of
per: Dzink-Fox, J., et al.
Publicat: (2017)

Clinicians’ views and experiences with offering and returning results from exome sequencing to parents of infants with hearing loss
per: Notini, L, et al.
Publicat: (2021)

Insights into platypus population structure and history from whole-genome sequencing
per: Martin, H, et al.
Publicat: (2018)

Old challenges or new issues? Genetic health professionals’ experiences obtaining informed consent in diagnostic genomic sequencing
per: Vears, VF, et al.
Publicat: (2020)

Diagnostic value of exome and whole genome sequencing in craniosynostosis
per: Miller, K, et al.
Publicat: (2016)

Whole genome sequencing of Mycobacterium tuberculosis
per: Cabibbe, A, et al.
Publicat: (2018)

Large-scale whole-genome sequencing of three diverse Asian populations in Singapore
per: Wu, Degang, et al.
Publicat: (2021)

Storing paediatric genomic data for sequential interrogation across the lifespan
per: Gyngell, C, et al.
Publicat: (2023)

Mutation mapping and identification by whole-genome sequencing
per: Leshchiner, Ignaty, et al.
Publicat: (2012)

11,670 whole-genome sequences representative of the Han Chinese population from the CONVERGE project.
per: Cai, N, et al.
Publicat: (2017)

Whole genome sequencing and resistance in Escherichia coli
per: Davies, T
Publicat: (2019)

Investigating the variability of virulence in natural populations of Staphylococcus aureus using whole genome sequencing
per: Young, B
Publicat: (2017)

Framework for quality assessment of whole genome cancer sequences
per: Whalley, JP, et al.
Publicat: (2020)

Resetting the bar: Statistical significance in whole-genome sequencing-based association studies of global populations
per: Pulit, S, et al.
Publicat: (2016)

Are whole-exome and whole-genome sequencing approaches cost-effective? A systematic review of the literature
per: Schwarze, K, et al.
Publicat: (2018)

Are whole exome and whole genome sequencing approaches cost-effective? A systematic review of the literature
per: Schwarze, K, et al.
Publicat: (2018)

The usefulness of whole genome sequencing in the management of Staphylococcus aureus infections.
per: Price, J, et al.
Publicat: (2013)

Whole Genome Sequencing in Twins Discordant for 27 Diseases
per: Ebers, G, et al.
Publicat: (2011)

Haemophilus influence: the impact of whole genome sequencing on microbiology.
per: Tang, C, et al.
Publicat: (1997)

Whole-genome sequencing of Aspergillus terreus species complex
per: Palanivel, Mathangi, et al.
Publicat: (2021)

The implementation of whole-genome sequencing for Mycobacterium tuberculosis in Vietnam
per: Huong, DT, et al.
Publicat: (2024)

Inferring whole-genome histories in large population datasets
per: Kelleher, J, et al.
Publicat: (2019)

Whole-genome sequencing of a sporadic primary immunodeficiency cohort
per: Thaventhiran, JED, et al.
Publicat: (2020)

Genome-wide association study using whole-genome sequencing identifies risk loci for Parkinson's disease in Chinese population
per: Pan, Hongxu, et al.
Publicat: (2024)

Whole genome sequencing in the prevention and control of Staphylococcus aureus infection.
per: Price, JR, et al.
Publicat: (2013)

Evolutionary history of Tibetans inferred from whole-genome sequencing.
per: Hu, H, et al.
Publicat: (2017)

Prediction of Staphylococcus aureus antimicrobial resistance by whole-genome sequencing
per: Gordon, N, et al.
Publicat: (2014)

Health professionals’ and researchers’ perspectives on prenatal whole genome and exome sequencing: ‘We can’t shut the door now, the genie’s out, we need to refine it’
per: Horn, R, et al.
Publicat: (2018)

Moving from ‘fully’ to ‘appropriately’ informed consent in genomics: the PROMICE framework
per: Koplin, J, et al.
Publicat: (2022)

Whole genome sequencing of Plasmodium falciparum from dried blood spots using selective whole genome amplification
per: Oyola, S, et al.
Publicat: (2016)

Bioinformatics and the Metaverse: Are we ready?
per: Taylor, S, et al.
Publicat: (2022)

Inference of homologous recombination in bacteria using whole-genome sequences.
per: Didelot, X, et al.
Publicat: (2010)

Whole-genome sequencing for predicting clarithromycin resistance in Mycobacterium abscessus
per: Lipworth, S, et al.
Publicat: (2018)

Investigation of in-hospital norovirus transmission using whole genome sequencing
per: Wong, THN
Publicat: (2014)

Whole-genome sequencing to determine Neisseria gonorrhoeae transmission: an observational study
per: De Silva, D, et al.
Publicat: (2016)

Whole-genome sequencing to determine transmission of Neisseria gonorrhoeae: an observational study
per: De Silva, D, et al.
Publicat: (2016)

Whole-genome sequencing for routine pathogen surveillance in public health: A population snapshot of invasive Staphylococcus aureus in Europe
per: Aanensen, DM, et al.
Publicat: (2016)