Cargando…

Clinical utilisation of a rapid low-pass whole genome sequencing technique for the diagnosis of aneuploidy in human embryos prior to implantation

BACKGROUND: The majority of human embryos created using in vitro fertilisation (IVF) techniques are aneuploid. Comprehensive chromosome screening methods, applicable to single cells biopsied from preimplantation embryos, allow reliable identification and transfer of euploid embryos. Recently, random...

Descripción completa

Detalles Bibliográficos
Autores principales:	Wells, Dagan, Kaur, Kulvinder, Grifo, Jamie, Glassner, Michael, Taylor, Jenny C, Fragouli, Elpida, Munne, Santiago
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BMJ Publishing Group 2014
Materias:	Methods
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4112454/ https://www.ncbi.nlm.nih.gov/pubmed/25031024 http://dx.doi.org/10.1136/jmedgenet-2014-102497

Ejemplares similares

Altered Levels of Mitochondrial DNA Are Associated with Female Age, Aneuploidy, and Provide an Independent Measure of Embryonic Implantation Potential
por: Fragouli, Elpida, et al.
Publicado: (2015)

Use of comprehensive chromosomal screening for embryo assessment: microarrays and CGH
por: Wells, Dagan, et al.
Publicado: (2008)

Embryos of Robertsonian Translocation Carriers Exhibit a Mitotic Interchromosomal Effect That Enhances Genetic Instability during Early Development
por: Alfarawati, Samer, et al.
Publicado: (2012)

Correction: Embryos of Robertsonian Translocation Carriers Exhibit a Mitotic Interchromosomal Effect That Enhances Genetic Instability during Early Development
por: Alfarawati, Samer, et al.
Publicado: (2022)

Detection and phasing of single base de novo mutations in biopsies from human in vitro fertilized embryos by advanced whole-genome sequencing
por: Peters, Brock A., et al.
Publicado: (2015)

Preimplantation Genetic Diagnosis for Aneuploidy and Translocations Using Array Comparative Genomic Hybridization
por: Munné, Santiago
Publicado: (2012)

Allele-specific copy number analysis of tumor samples with aneuploidy and tumor heterogeneity
por: Rasmussen, Markus, et al.
Publicado: (2011)

Detecting, quantifying, and discriminating the mechanism of mosaic chromosomal aneuploidies using MAD-seq
por: Kong, Yu, et al.
Publicado: (2018)

Single-pass transcription by T7 RNA polymerase
por: Passalacqua, Luiz F.M., et al.
Publicado: (2020)

Permission to pass: on the role of p53 as a gatekeeper for aneuploidy
por: Marques, Joana F., et al.
Publicado: (2023)

Characterization and quantification of proteins secreted by single human embryos prior to implantation
por: Poli, Maurizio, et al.
Publicado: (2015)

Noninvasive prenatal testing for fetal subchromosomal copy number variations and chromosomal aneuploidy by low‐pass whole‐genome sequencing
por: Yu, Dongyi, et al.
Publicado: (2019)

Flat mount preparation for whole-mount fluorescent imaging of zebrafish embryos
por: Frommelt, Joseph, et al.
Publicado: (2023)

Correlation study of male semen parameters and embryo aneuploidy in preimplantation genetic testing for aneuploidy
por: Yang, Hongyi, et al.
Publicado: (2023)

The effect of sperm DNA fragmentation on the incidence and origin of whole and segmental chromosomal aneuploidies in human embryos
por: Gao, Jiangman, et al.
Publicado: (2023)

Chromosome-scale mega-haplotypes enable digital karyotyping of cancer aneuploidy
por: Bell, John M., et al.
Publicado: (2017)

An engineered mammalian band-pass network
por: Greber, David, et al.
Publicado: (2010)

Utilization of standardized preimplantation genetic testing for aneuploidy (PGT-A) via artificial intelligence (AI) technology is correlated with improved pregnancy outcomes in single thawed euploid embryo transfer (STEET) cycles
por: Buldo-Licciardi, Julia, et al.
Publicado: (2023)

Preimplantation genetic testing for aneuploidy: The management of mosaic embryos
por: Yu, Eun Jeong, et al.
Publicado: (2022)

Is there an androgen level threshold for aneuploidy risk in infertile women?
por: Gleicher, Norbert, et al.
Publicado: (2015)

BubbleTree: an intuitive visualization to elucidate tumoral aneuploidy and clonality using next generation sequencing data
por: Zhu, Wei, et al.
Publicado: (2016)

Automated staging of zebrafish embryos with deep learning
por: Jones, Rebecca A, et al.
Publicado: (2023)

Micro-scale Experimental System Coupled with Fluorescence-based Estimation of Fungal Biomass to Study Utilisation of Plant Substrates
por: Németh, Julianna B., et al.
Publicado: (2021)

Parental chromosomal heteromorphisms are not associated with an increased risk of embryo aneuploidy
por: Hernandez-Nieto, Carlos, et al.
Publicado: (2021)

Accuracy and depth evaluation of clinical low pass genome sequencing in the detection of mosaic aneuploidies and CNVs
por: Liu, Yanqiu, et al.
Publicado: (2023)

RNA-seq as a tool for evaluating human embryo competence
por: Groff, Abigail F., et al.
Publicado: (2019)

Mendelian randomization with Egger pleiotropy correction and weakly informative Bayesian priors
por: Schmidt, A F, et al.
Publicado: (2018)

Utilising polymorphisms to achieve allele-specific genome editing in zebrafish
por: Capon, Samuel J., et al.
Publicado: (2016)

Live Birth from Previously Vitrified Oocytes, After Trophectoderm Biopsy, Revitrification, and Transfer of a Euploid Blastocyst
por: Grifo, Jamie A., et al.
Publicado: (2013)

Computational discovery of cis-regulatory modules in Drosophila without prior knowledge of motifs
por: Ivan, Andra, et al.
Publicado: (2008)

Causal integration of multi‐omics data with prior knowledge to generate mechanistic hypotheses
por: Dugourd, Aurelien, et al.
Publicado: (2021)

Structure supports function: Informing directed and dynamic functional connectivity with anatomical priors
por: Pascucci, David, et al.
Publicado: (2022)

Analysis of aneuploidy in first-cleavage mouse embryos fertilized in vitro and in vivo.
por: Fraser, L R, et al.
Publicado: (1979)

Aneuploidy and DNA Methylation as Mirrored Features of Early Human Embryo Development
por: Tolmacheva, Ekaterina N., et al.
Publicado: (2020)

Erratum to: Comment on: Gleicher N et al.,2016. Reprod biol endocrinol Sep 5;14(1):54
por: Tiegs, Ashley W., et al.
Publicado: (2017)

Response to comment on: Gleicher N et al., 2016. Reprod biol endocrinol Sep 5;14(1):54
por: Tiegs, Ashley W., et al.
Publicado: (2017)

Latent feature extraction with a prior-based self-attention framework for spatial transcriptomics
por: Li, Zhen, et al.
Publicado: (2023)

CATI: an efficient gene integration method for rodent and primate embryos by MMEJ suppression
por: Chen, Hongyu, et al.
Publicado: (2023)

Utilising a novel surveillance system to enhance field screening activities for the leishmaniases
por: Panahi, Elina, et al.
Publicado: (2020)

Bayesian estimation of cell type–specific gene expression with prior derived from single-cell data
por: Wang, Jiebiao, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_b5ehtloqd9p048rtr917nkvuv1