Clinical utilisation of a rapid low-pass whole genome sequencing technique for the diagnosis of aneuploidy in human embryos prior to implantation
about
Preimplantation genetic diagnosis of hemophilia AWhole genome amplification with SurePlex results in better copy number alteration detection using sequencing data compared to the MALBAC methodTowards clinical application of pronuclear transfer to prevent mitochondrial DNA disease.The accumulation of vitrified oocytes is a strategy to increase the number of euploid available blastocysts for transfer after preimplantation genetic testing.Identification of mosaic and segmental aneuploidies by next-generation sequencing in preimplantation genetic screening can improve clinical outcomes compared to array-comparative genomic hybridization.Rapid Short-Read Sequencing and Aneuploidy Detection Using MinION Nanopore TechnologyDetection and phasing of single base de novo mutations in biopsies from human in vitro fertilized embryos by advanced whole-genome sequencingAltered levels of mitochondrial DNA are associated with female age, aneuploidy, and provide an independent measure of embryonic implantation potential.Increasing live birth rate by preimplantation genetic screening of pooled polar bodies using array comparative genomic hybridizationRandomized comparison of next-generation sequencing and array comparative genomic hybridization for preimplantation genetic screening: a pilot studyManagement of Incidental Findings in the Era of Next-generation SequencingPreimplantation genetic screening of blastocysts by multiplex qPCR followed by fresh embryo transfer: validation and verificationOocyte mitochondrial function and reproduction.Is the presence of an uncleaved embryo on day 3 a useful predictor of outcomes following day 5 transfer?Healthy Baby Born to a Robertsonian Translocation Carrier following Next-Generation Sequencing-Based Preimplantation Genetic Diagnosis: A Case Report.Mitochondrial DNA quantification as a tool for embryo viability assessment: retrospective analysis of data from single euploid blastocyst transfers.New protocol based on massive parallel sequencing for aneuploidy screening of preimplantation human embryos.Identification of small segmental translocations in patients with repeated implantation failure and recurrent miscarriage using next generation sequencing after in vitro fertilization/intracytoplasmic sperm injection.Live births after simultaneous avoidance of monogenic diseases and chromosome abnormality by next-generation sequencing with linkage analysesA pilot proof-of-principle study to compare fresh and vitrified cycle preimplantation genetic screening by chromosome microarray and next generation sequencing.Clinical application of next-generation sequencing in preimplantation genetic diagnosis cycles for Robertsonian and reciprocal translocations.Single cell sequencing: a distinct new field.Differences in pregnancy outcomes in donor egg frozen embryo transfer (FET) cycles following preimplantation genetic screening (PGS): a single center retrospective study.mtDNA mutations variously impact mtDNA maintenance throughout the human embryofetal development.Analysis of implantation and ongoing pregnancy rates following the transfer of mosaic diploid-aneuploid blastocysts.Elective Single Embryo Transfer: an update to UK Best Practice Guidelines.The role of experiential knowledge within attitudes towards genetic carrier screening: A comparison of people with and without experience of spinal muscular atrophy.Next Generation Sequencing-Based Comprehensive Chromosome Screening in Mouse Polar Bodies, Oocytes, and Embryos.Ovarian ageing: the role of mitochondria in oocytes and follicles.The why, the how and the when of PGS 2.0: current practices and expert opinions of fertility specialists, molecular biologists, and embryologistsEuploidy rates in donor egg cycles significantly differ between fertility centers.Human embryo mosaicism: did we drop the ball on chromosomal testing?Prenatal and pre-implantation genetic diagnosis.Next-generation molecular diagnosis: single-cell sequencing from bench to bedside.The mitochondrial DNA content of cumulus granulosa cells is linked to embryo quality.Polymorphisms in the MTHFR gene influence embryo viability and the incidence of aneuploidy.Performance of four modern whole genome amplification methods for copy number variant detection in single cells.Reproductive aging is associated with changes in oocyte mitochondrial dynamics, function, and mtDNA quantity.Response to comment on: Gleicher N et al., 2016. Reprod biol endocrinol Sep 5;14(1):54.Chromosomal Aneuploidy Improves the Brewing Characteristics of Sake Yeast.
P2860
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P2860
Clinical utilisation of a rapid low-pass whole genome sequencing technique for the diagnosis of aneuploidy in human embryos prior to implantation
description
2014 nî lūn-bûn
@nan
2014 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Clinical utilisation of a rapi ...... embryos prior to implantation
@ast
Clinical utilisation of a rapi ...... embryos prior to implantation
@en
type
label
Clinical utilisation of a rapi ...... embryos prior to implantation
@ast
Clinical utilisation of a rapi ...... embryos prior to implantation
@en
prefLabel
Clinical utilisation of a rapi ...... embryos prior to implantation
@ast
Clinical utilisation of a rapi ...... embryos prior to implantation
@en
P2093
P2860
P50
P1476
Clinical utilisation of a rapi ...... embryos prior to implantation
@en
P2093
Dagan Wells
Elpida Fragouli
Kulvinder Kaur
Michael Glassner
P2860
P304
P356
10.1136/JMEDGENET-2014-102497
P407
P577
2014-08-01T00:00:00Z