Identification of chromosomal errors in human preimplantation embryos with oligonucleotide DNA microarray.

A previous study comparing the performance of different platforms for DNA microarray found that the oligonucleotide (oligo) microarray platform containing 385K isothermal probes had the best performance when evaluating dosage sensitivity, precision, specificity, sensitivity and copy number variation...

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Main Authors: Lifeng Liang, Cassie T Wang, Xiaofang Sun, Lian Liu, Man Li, Craig Witz, Daniel Williams, Jason Griffith, Josh Skorupski, Ghassan Haddad, Jimmy Gill, Wei-Hua Wang
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3628862?pdf=render
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spelling doaj-e6075fdd8c0f4d5a9bb6c94c78ecb1f72020-11-25T02:42:28ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0184e6183810.1371/journal.pone.0061838Identification of chromosomal errors in human preimplantation embryos with oligonucleotide DNA microarray.Lifeng LiangCassie T WangXiaofang SunLian LiuMan LiCraig WitzDaniel WilliamsJason GriffithJosh SkorupskiGhassan HaddadJimmy GillWei-Hua WangA previous study comparing the performance of different platforms for DNA microarray found that the oligonucleotide (oligo) microarray platform containing 385K isothermal probes had the best performance when evaluating dosage sensitivity, precision, specificity, sensitivity and copy number variations border definition. Although oligo microarray platform has been used in some research fields and clinics, it has not been used for aneuploidy screening in human embryos. The present study was designed to use this new microarray platform for preimplantation genetic screening in the human. A total of 383 blastocysts from 72 infertility patients with either advanced maternal age or with previous miscarriage were analyzed after biopsy and microarray. Euploid blastocysts were transferred to patients and clinical pregnancy and implantation rates were measured. Chromosomes in some aneuploid blastocysts were further analyzed by fluorescence in-situ hybridization (FISH) to evaluate accuracy of the results. We found that most (58.1%) of the blastocysts had chromosomal abnormalities that included single or multiple gains and/or losses of chromosome(s), partial chromosome deletions and/or duplications in both euploid and aneuploid embryos. Transfer of normal euploid blastocysts in 34 cycles resulted in 58.8% clinical pregnancy and 54.4% implantation rates. Examination of abnormal blastocysts by FISH showed that all embryos had matching results comparing microarray and FISH analysis. The present study indicates that oligo microarray conducted with a higher resolution and a greater number of probes is able to detect not only aneuploidy, but also minor chromosomal abnormalities, such as partial chromosome deletion and/or duplication in human embryos. Preimplantation genetic screening of the aneuploidy by DNA microarray is an advanced technology used to select embryos for transfer and improved embryo implantation can be obtained after transfer of the screened normal embryos.http://europepmc.org/articles/PMC3628862?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Lifeng Liang
Cassie T Wang
Xiaofang Sun
Lian Liu
Man Li
Craig Witz
Daniel Williams
Jason Griffith
Josh Skorupski
Ghassan Haddad
Jimmy Gill
Wei-Hua Wang
spellingShingle Lifeng Liang
Cassie T Wang
Xiaofang Sun
Lian Liu
Man Li
Craig Witz
Daniel Williams
Jason Griffith
Josh Skorupski
Ghassan Haddad
Jimmy Gill
Wei-Hua Wang
Identification of chromosomal errors in human preimplantation embryos with oligonucleotide DNA microarray.
PLoS ONE
author_facet Lifeng Liang
Cassie T Wang
Xiaofang Sun
Lian Liu
Man Li
Craig Witz
Daniel Williams
Jason Griffith
Josh Skorupski
Ghassan Haddad
Jimmy Gill
Wei-Hua Wang
author_sort Lifeng Liang
title Identification of chromosomal errors in human preimplantation embryos with oligonucleotide DNA microarray.
title_short Identification of chromosomal errors in human preimplantation embryos with oligonucleotide DNA microarray.
title_full Identification of chromosomal errors in human preimplantation embryos with oligonucleotide DNA microarray.
title_fullStr Identification of chromosomal errors in human preimplantation embryos with oligonucleotide DNA microarray.
title_full_unstemmed Identification of chromosomal errors in human preimplantation embryos with oligonucleotide DNA microarray.
title_sort identification of chromosomal errors in human preimplantation embryos with oligonucleotide dna microarray.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description A previous study comparing the performance of different platforms for DNA microarray found that the oligonucleotide (oligo) microarray platform containing 385K isothermal probes had the best performance when evaluating dosage sensitivity, precision, specificity, sensitivity and copy number variations border definition. Although oligo microarray platform has been used in some research fields and clinics, it has not been used for aneuploidy screening in human embryos. The present study was designed to use this new microarray platform for preimplantation genetic screening in the human. A total of 383 blastocysts from 72 infertility patients with either advanced maternal age or with previous miscarriage were analyzed after biopsy and microarray. Euploid blastocysts were transferred to patients and clinical pregnancy and implantation rates were measured. Chromosomes in some aneuploid blastocysts were further analyzed by fluorescence in-situ hybridization (FISH) to evaluate accuracy of the results. We found that most (58.1%) of the blastocysts had chromosomal abnormalities that included single or multiple gains and/or losses of chromosome(s), partial chromosome deletions and/or duplications in both euploid and aneuploid embryos. Transfer of normal euploid blastocysts in 34 cycles resulted in 58.8% clinical pregnancy and 54.4% implantation rates. Examination of abnormal blastocysts by FISH showed that all embryos had matching results comparing microarray and FISH analysis. The present study indicates that oligo microarray conducted with a higher resolution and a greater number of probes is able to detect not only aneuploidy, but also minor chromosomal abnormalities, such as partial chromosome deletion and/or duplication in human embryos. Preimplantation genetic screening of the aneuploidy by DNA microarray is an advanced technology used to select embryos for transfer and improved embryo implantation can be obtained after transfer of the screened normal embryos.
url http://europepmc.org/articles/PMC3628862?pdf=render
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