Literature DB >> 9238681

Adaptation of the primer extension preamplification (PEP) reaction for preimplantation diagnosis: single blastomere analysis using short PEP protocols.

K Sermon1, W Lissens, H Joris, A Van Steirteghem, I Liebaers.   

Abstract

Primer extension preamplification (PEP) was first described as a method for whole genome amplification, starting from a single cell, originally a spermatozoon, in order to perform genetic recombination studies. Its usefulness for preimplantation diagnosis was shown soon after; the only drawback was the length of the procedure (> 14 h). We have developed a shorter PEP protocol for single human blastomeres, enabling us to examine several genetic loci of interest in human genetic diseases with a good amplification efficiency.

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Year:  1996        PMID: 9238681     DOI: 10.1093/molehr/2.3.209

Source DB:  PubMed          Journal:  Mol Hum Reprod        ISSN: 1360-9947            Impact factor:   4.025


  9 in total

Review 1.  Molecular diagnostics in preimplantation genetic diagnosis.

Authors:  Alan R Thornhill; Karen Snow
Journal:  J Mol Diagn       Date:  2002-02       Impact factor: 5.568

Review 2.  Whole genome amplification in preimplantation genetic diagnosis.

Authors:  Ying-ming Zheng; Ning Wang; Lei Li; Fan Jin
Journal:  J Zhejiang Univ Sci B       Date:  2011-01       Impact factor: 3.066

Review 3.  Review: preimplantation diagnosis of inherited disease.

Authors:  W Lissens; K Sermon; C Staessen; E V Assche; C Janssenswillen; H Joris; A Van Steirteghem; I Liebaers
Journal:  J Inherit Metab Dis       Date:  1996       Impact factor: 4.982

Review 4.  Whole Genome Amplification in Preimplantation Genetic Testing in the Era of Massively Parallel Sequencing.

Authors:  Ludmila Volozonoka; Anna Miskova; Linda Gailite
Journal:  Int J Mol Sci       Date:  2022-04-27       Impact factor: 6.208

5.  New array approaches to explore single cells genomes.

Authors:  Evelyne Vanneste; Lilach Bittman; Niels Van der Aa; Thierry Voet; Joris Robert Vermeesch
Journal:  Front Genet       Date:  2012-03-27       Impact factor: 4.599

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

Authors:  Lieselot Deleye; Dieter De Coninck; Christodoulos Christodoulou; Tom Sante; Annelies Dheedene; Björn Heindryckx; Etienne Van den Abbeel; Petra De Sutter; Björn Menten; Dieter Deforce; Filip Van Nieuwerburgh
Journal:  Sci Rep       Date:  2015-06-30       Impact factor: 4.379

Review 7.  Microfluidics for genome-wide studies involving next generation sequencing.

Authors:  Sai Ma; Travis W Murphy; Chang Lu
Journal:  Biomicrofluidics       Date:  2017-03-10       Impact factor: 2.800

Review 8.  Recent advances and application of whole genome amplification in molecular diagnosis and medicine.

Authors:  Xiaoyu Wang; Yapeng Liu; Hongna Liu; Wenjing Pan; Jie Ren; Xiangming Zheng; Yimin Tan; Zhu Chen; Yan Deng; Nongyue He; Hui Chen; Song Li
Journal:  MedComm (2020)       Date:  2022-02-03

9.  Detection of chromosomal structural alterations in single cells by SNP arrays: a systematic survey of amplification bias and optimized workflow.

Authors:  Kazuya Iwamoto; Miki Bundo; Junko Ueda; Yoko Nakano; Wataru Ukai; Eri Hashimoto; Toshikazu Saito; Tadafumi Kato
Journal:  PLoS One       Date:  2007-12-12       Impact factor: 3.240

  9 in total

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