Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Accurate single cell 24 chromosome aneuploidy screening using whole genome amplification and single nucleotide polymorphism microarrays.

Fertility and sterility - 1 Nov 2010

Treff Nathan R, Su Jing, Tao Xin, Levy Brynn, Scott Richard T

Abstract excerpt

OBJECTIVE: To develop and validate a whole genome amplification and single nucleotide polymorphism (SNP) microarray protocol for accurate single cell 24 chromosome aneuploidy screening. DESIGN: Prospective, randomized, and blinded study. SETTING: Academic reproductive medicine center. PATIENT(S):...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Aneuploidy
Share to Chromosomes, Human
Share to Genome

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Loss of Heterozygosity

Share to Nucleic Acid Amplification Techniques

Share to Oligonucleotide Array Sequence Analysis

Share to Predictive Value of Tests

Share to Preimplantation Diagnosis

Source

Identifiers

PMID: 20188357
DOI: 10.1016/j.fertnstert.2010.01.052

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20188357-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Accurate single cell 24 chromosome aneuploidy screening using whole genome amplification and single nucleotide polymorphism microarrays.PMID 20188357Read ↗

Preclinical validation of a microarray method for full molecular karyotyping of blastomeres in a 24-h protocolSemantic proximity Read ↗

Single nucleotide polymorphism microarray-based concurrent screening of 24-chromosome aneuploidy and unbalanced translocations in preimplantation human embryos.Semantic proximity Read ↗

Comparison of array comparative genomic hybridization and quantitative real-time PCR-based aneuploidy screening of blastocyst biopsies.Semantic proximity Read ↗

SNP microarray-based 24 chromosome aneuploidy screening is significantly more consistent than FISH.Semantic proximity Read ↗

Preclinical validation of a targeted next generation sequencing-based comprehensive chromosome screening methodology in human blastocystsSemantic proximity Read ↗

Pregnancy outcomes from more than 1,800 in vitro fertilization cycles with the use of 24-chromosome single-nucleotide polymorphism-based preimplantation genetic testing for aneuploidy.Semantic proximity Read ↗

The role of preimplantation genetic diagnosis in diagnosing embryo aneuploidySemantic proximity Read ↗

PGD and aneuploidy screening for 24 chromosomes: advantages and disadvantages of competing platforms.Semantic proximity Read ↗

Mosaic autosomal aneuploidies are detectable from single-cell RNAseq data.Semantic proximity Read ↗

Detection of Chromosomal Aneuploidy in Human Preimplantation Embryos by Next-Generation Sequencing1Semantic proximity Read ↗

Single-cell whole-genome amplification technique impacts the accuracy of SNP microarray-based genotyping and copy number analyses.Semantic proximity Read ↗

24-chromosome PCR for aneuploidy screeningSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.