Systematic assessment of the performance of whole-genome amplification for SNP/CNV detection and β-thalassemia genotyping

Assisted reproductive technology in Europe, 2012: results generated from European registers by ESHRE

(2016)   HUMAN REPRODUCTION

The clinical application of preimplantation genetic diagnosis for the patient affected by congenital contractural arachnodactyly and spinal and bulbar muscular atrophy

(2016) Linjun Chen et al.   JOURNAL OF ASSISTED REPRODUCTION AND GENETICS

Clinical application of next-generation sequencing in preimplantation genetic diagnosis cycles for Robertsonian and reciprocal translocations

(2016) Wenke Zhang et al.   JOURNAL OF ASSISTED REPRODUCTION AND GENETICS

Highly multiplexed targeted DNA sequencing from single nuclei

(2016) Marco L Leung et al.   Nature Protocols

Comparison of three whole genome amplification methods for detection of genomic aberrations in single cells

(2016) Elizabeth Normand et al.   PRENATAL DIAGNOSIS

Comparative study of whole genome amplification and next generation sequencing performance of single cancer cells

(2016) Anna Babayan et al.   Oncotarget

Performance of a TthPrimPol-based whole genome amplification kit for copy number alteration detection using massively parallel sequencing

(2016) Lieselot Deleye et al.   Scientific Reports

The Performance of Whole Genome Amplification Methods and Next-Generation Sequencing for Pre-Implantation Genetic Diagnosis of Chromosomal Abnormalities

(2015) Na Li et al.   Journal of Genetics and Genomics

Challenges in prenatal diagnosis of beta thalassaemia: couples with normal HbA2in one partner

(2015) Manju Gorivale et al.   PRENATAL DIAGNOSIS

Live births after simultaneous avoidance of monogenic diseases and chromosome abnormality by next-generation sequencing with linkage analyses

(2015) Liying Yan et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Whole genome amplification with SurePlex results in better copy number alteration detection using sequencing data compared to the MALBAC method

(2015) Lieselot Deleye et al.   Scientific Reports

Genome Analyses of Single Human Oocytes

(2013) Yu Hou et al.   CELL

Obstetric and perinatal outcomes in singleton pregnancies resulting from the transfer of blastocyst-stage versus cleavage-stage embryos generated through in vitro fertilization treatment: a systematic review and meta-analysis

(2013) Abha Maheshwari et al.   FERTILITY AND STERILITY

Cleavage-stage biopsy significantly impairs human embryonic implantation potential while blastocyst biopsy does not: a randomized and paired clinical trial

(2013) Richard T. Scott et al.   FERTILITY AND STERILITY

Single-cell paired-end genome sequencing reveals structural variation per cell cycle

(2013) Thierry Voet et al.   NUCLEIC ACIDS RESEARCH

First successful double-factor PGD for Lynch syndrome: monogenic analysis and comprehensive aneuploidy screening

(2012) G Daina et al.   CLINICAL GENETICS

Genome-Wide Detection of Single-Nucleotide and Copy-Number Variations of a Single Human Cell

(2012) C. Zong et al.   SCIENCE

Probing Meiotic Recombination and Aneuploidy of Single Sperm Cells by Whole-Genome Sequencing

(2012) S. Lu et al.   SCIENCE

A Melting Curve Analysis–Based PCR Assay for One-Step Genotyping of β-Thalassemia Mutations

(2011) Fu Xiong et al.   JOURNAL OF MOLECULAR DIAGNOSTICS

Whole genome amplification in preimplantation genetic diagnosis

(2011) Ying-ming Zheng et al.   Journal of Zhejiang University-SCIENCE B

Molecular epidemiological survey of haemoglobinopathies in the Guangxi Zhuang Autonomous Region of southern China

(2010) F Xiong et al.   CLINICAL GENETICS

Evaluation of genome coverage and fidelity of multiple displacement amplification from single cells by SNP array

(2009) J. Ling et al.   MOLECULAR HUMAN REPRODUCTION

Vitrification of biopsied embryos at cleavage, morula and blastocyst stage

(2009) Xiao Zhang et al.   REPRODUCTIVE BIOMEDICINE ONLINE