<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Schaeffer E</submitter><funding>Consejo Nacional de Ciencia y Tecnología</funding><pagination>1209158</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5498896</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>2017</volume><pubmed_abstract>Our objective was to determine if whole genome amplification (WGA) provides suitable DNA for qPCR-based genotyping for human embryos. Single blastomeres (Day 3) or trophoblastic cells (Day 5) were isolated from 342 embryos for WGA. Comparative Genomic Hybridization determined embryo sex as well as Trisomy 18 or Trisomy 21. To determine the embryo's sex, qPCR melting curve analysis for SRY and DYS14 was used. Logistic regression indicated a 4.4%, 57.1%, or 98.8% probability of a male embryo when neither gene, SRY only, or both genes were detected, respectively (accuracy = 94.1%, kappa = 0.882, and &lt;i>p&lt;/i> &lt; 0.001). Fluorescent Capillary Electrophoresis for the amelogenin genes (AMEL) was also used to determine sex. AMELY peak's height was higher and this peak's presence was highly predicti</pubmed_abstract><journal>BioMed research international</journal><pubmed_title>Whole Genome Amplification of Day 3 or Day 5 Human Embryos Biopsies Provides a Suitable DNA Template for PCR-Based Techniques for Genotyping, a Complement of Preimplantation Genetic Testing.</pubmed_title><pmcid>PMC5498896</pmcid><funding_grant_id>212650</funding_grant_id><funding_grant_id>231793</funding_grant_id><pubmed_authors>Camargo F</pubmed_authors><pubmed_authors>Schaeffer E</pubmed_authors><pubmed_authors>Camacho R</pubmed_authors><pubmed_authors>Neumann A</pubmed_authors><pubmed_authors>Gomez R</pubmed_authors><pubmed_authors>Lopez-Bayghen B</pubmed_authors><pubmed_authors>Porchia LM</pubmed_authors><pubmed_authors>Garrido E</pubmed_authors><pubmed_authors>Lopez-Bayghen E</pubmed_authors></additional><is_claimable>false</is_claimable><name>Whole Genome Amplification of Day 3 or Day 5 Human Embryos Biopsies Provides a Suitable DNA Template for PCR-Based Techniques for Genotyping, a Complement of Preimplantation Genetic Testing.</name><description>Our objective was to determine if whole genome amplification (WGA) provides suitable DNA for qPCR-based genotyping for human embryos. Single blastomeres (Day 3) or trophoblastic cells (Day 5) were isolated from 342 embryos for WGA. Comparative Genomic Hybridization determined embryo sex as well as Trisomy 18 or Trisomy 21. To determine the embryo's sex, qPCR melting curve analysis for SRY and DYS14 was used. Logistic regression indicated a 4.4%, 57.1%, or 98.8% probability of a male embryo when neither gene, SRY only, or both genes were detected, respectively (accuracy = 94.1%, kappa = 0.882, and &lt;i>p&lt;/i> &lt; 0.001). Fluorescent Capillary Electrophoresis for the amelogenin genes (AMEL) was also used to determine sex. AMELY peak's height was higher and this peak's presence was highly predicti</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017</publication><modification>2026-05-05T11:05:14.924Z</modification><creation>2019-03-27T02:49:33Z</creation></dates><accession>S-EPMC5498896</accession><cross_references><pubmed>28717645</pubmed><doi>10.1155/2017/1209158</doi></cross_references></HashMap>