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

The Performance of Whole Genome Amplification Methods and Next-Generation Sequencing for Pre-Implantation Genetic Diagnosis of Chromosomal Abnormalities

14 Mar 2015

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Molecular Biology Techniques and Applications
Share to Organ and Tissue Transplantation Research
Share to Prenatal Screening and Diagnostics

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 25953353
DOI: 10.1016/j.jgg.2015.03.001

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The Performance of Whole Genome Amplification Methods and Next-Generation Sequencing for Pre-Implantation Genetic Diagnosis of Chromosomal AbnormalitiesPMID 25953353Read ↗

A Novel and Comprehensive Whole-Genome Sequencing–Based Preimplantation Genetic Testing Approach for Different Genetic ConditionsSemantic proximity Read ↗

Evaluation of chromosomal abnormalities from preimplantation genetic testing to the reproductive outcomes: a comparison between three different structural rearrangements based on next-generation sequencingSemantic proximity Read ↗

Development and validation of concurrent preimplantation genetic diagnosis for single gene disorders and comprehensive chromosomal aneuploidy screening without whole genome amplificationSemantic proximity Read ↗

Evaluation of preimplantation genetic testing for chromosomal structural rearrangement by a commonly used next generation sequencing workflowSemantic proximity Read ↗

A review of pre-implantation genetic testing technologies and applicationsSemantic proximity Read ↗

Preimplantation genetic testing for complex chromosomal rearrangement carriers by next-generation sequencingSemantic proximity Read ↗

Next-generation sequencing for preimplantation genetic diagnosisSemantic proximity Read ↗

The impact of next-generation sequencing technology on preimplantation genetic diagnosis and screeningSemantic proximity Read ↗

Whole genome sequencing vs chromosomal microarray analysis in prenatal diagnosisSemantic proximity Read ↗

Whole genome amplification from single cells in preimplantation genetic diagnosis and prenatal diagnosisSemantic proximity Read ↗

Noninvasive prenatal screening (NIPS) for fetal chromosome abnormalities in a general-risk population: An evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG)Semantic proximity Read ↗

Noninvasive prenatal screening (NIPS) for fetal chromosome abnormalities in a general-risk population: An evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG)Semantic proximity Read ↗

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