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E-GEOD-44994 GSE44994 genotyping by array, comparative genomi… Homo sapiens

SNP microarray-based PGS significantly improves the clinical outcome for translocation carriers

·Released March 11, 2013 ·Updated June 2, 2014
32
Samples
32
Assays
1
Array Platforms
Description

This was a retrospective comparison study of SNP-based preimplantation genetic screening (SNP-PGS) and FISH-based preimplantation genetic diagnosis (FISH-PGD) for 575 couples in total with chromosome translocations, including 169 couples treated by SNP-PGS between October 2011 and August 2012, and 406 couples treated by FISH- PGD between January 2005 and October 2011. In total, 773 blastocysts obtained from 169 couples were biopsied and frozen, embryo transfer was carried out on the balanced embryos. The PGS results and pregnancy outcomes were compared with those of FISH-PGD for 406 translocation carriers with 3,968 embryos biopsied on day 3. Of the 773 biopsied blastocysts, reliable SNP-PGS results were obtained for 717 (92.76%). For Robertsonian translocation carriers, the rate of normal/balanced embryos, embryos with translocation-related abnormalities, and embryos with abnormalities unrelated to a translocation were 57.80%, 23.39% and 18.81%, respectively. In reciprocal translocation carriers, the rate of normal/balanced embryos, embryos with translocation-related abnormalities and embryos with abnormalities unrelated to translocation were 35.47%, 52.10% and 12.42%, respectively. There was no significant differences in patient age, basal endocrine level and the average number of retrieved oocytes and good quality day 3 embryos before biopsy in the SNP-PGS group compared with the FISH-PGD group. The number of embryos biopsied in the FISH-PGD group was higher than in the SNP-PGS group. However, the pregnancy rate with successful delivery per oocyte retrieval and the implantation rate were both lower in the FISH-PGD group than in the SNP-PGS group. The spontaneous abortion rate was higher in the FISH-PGD group than in the SNP-PGS group. Affymetrix SNP arrays were performed according to the manufacturer's directions on DNA extracted from trophectoderm cells.

Array Platforms
A-AFFY-107
Affymetrix GeneChip Human Mapping 250K Array Nsp [Mapping250K_Nsp](32 items)
Sample Attributes
analysis result
45,XX,+20(q13.13),-22, 45,XY,+2q,-14, 45,XY,-15, 45,XY,-22, 46,XX, 46,XX,+19, 46,XX,+2(pter-p16.2),-4(q32.1qter),-7(pter-p14.1), 46,XX,+9(pter-q33),-12(pter-q23), 46,XX,-6(q12-qter),+9(p22-p11.3),+10(q21.2-q23.1),-16(q23.1-qter),+18(q12.1-q21.1),-19(pter-p13.11),-22(q11.2-qter), 46,XX,-6(q16.3-qter),-22, 46,XY, 46,XY,+3(q26.31-qter), 46,XY,+3p, 47,XY,+9,-10(pter-q25),-17,-18,+20,+21,+21,+22, 48,XX,+21,+22, XX,+1(q31-qter);-2(q32-qter),-7
cell type
trophectoderm cells
karyotype classification
reciprocal translocation, Robertsonian translocation
karyotype of patient donor
45,XX,der(13;14)(q10;q10), 45,XX,der(14;21)(q10;q10), 45,XY,der(13;14)(q10;q10), 45,XY,der(13;15)(q10;q10), 45,XY,t(13;14)(q10;q10), 46,XX,t(1;2)(q23;q31), 46,XX,t(3;6)(p25;q21), 46,XX,t(7;19)(q11;q13), 46,XX,t(9;12)(q32;q22), 46,XX,t(9;13)(q32;q14), 46,XY,t(10;15)(q22;q24), 46,XY,t(11;22)(q23;q11.2), 46,XY,t(1;17)(p22;q21), 46,XY,t(1;6)(q42;q25), 46,XY,t(2;6)(q35;q21), 46,XY,t(2;7)(p13;p13), 46,XY,t(3;17)(q13;p11), 46,XY,t(4;15)(q31;q12), 46,XY,t(6;22)(q12;p11.2), 46,XY,t(6;7)(q21;q22), 46,XY,t(6;8)(q21;q24.1)
Organism
Homo sapiens
result classification
complex aneuploid, De novo aneuploidy, De novo aneuploidy and segmental abnormality, De novo segmental abnormality, normal female, normal male, Unbalanced translocation, Unbalanced translocation and de novo aneuploidy, Unbalanced translocation and de novo segmental abnormality
Experiment Info
Accession
E-GEOD-44994
GEO ID
GSE44994
Type
genotyping by array, comparative genomic hybridization by array
Organism
Homo sapiens
Released
March 11, 2013
Updated
June 2, 2014
Submitter
Guang X Lu、 xiong bo、 Yue Q Tan
Analysis Services
Analysis Services

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