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

Validation of a targeted next generation sequencing-based comprehensive chromosome screening platform for detection of triploidy in human blastocysts

2 Jan 2018

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 Gestational Trophoblastic Disease Studies
Share to Prenatal Screening and Diagnostics
Share to Reproductive Biology and Fertility

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 29366772
DOI: 10.1016/j.rbmo.2017.12.015

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

Validation of a targeted next generation sequencing-based comprehensive chromosome screening platform for detection of triploidy in human blastocystsPMID 29366772Read ↗

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

Shallow whole genome sequencing is well suited for the detection of chromosomal aberrations in human blastocystsSemantic proximity Read ↗

Validation of next-generation sequencing for comprehensive chromosome screening of embryosSemantic proximity Read ↗

Validation of a next-generation sequencing–based protocol for 24-chromosome aneuploidy screening of blastocystsSemantic proximity Read ↗

24-chromosome PCR for aneuploidy screeningSemantic proximity Read ↗

Distribution patterns of segmental aneuploidies in human blastocysts identified by next-generation sequencingSemantic proximity Read ↗

Prevalence and authenticity of de-novo segmental aneuploidy (>16 Mb) in human blastocysts as detected by next-generation sequencingSemantic proximity Read ↗

Development and validation of a next-generation sequencing–based protocol for 24-chromosome aneuploidy screening of embryosSemantic proximity Read ↗

Reanalysis of human blastocysts with different molecular genetic screening platforms reveals significant discordance in ploidy statusSemantic proximity Read ↗

Massively parallel sequencing for chromosomal abnormality testing in trophectoderm cells of human blastocysts.Semantic proximity Read ↗

Application of next-generation sequencing technology for comprehensive aneuploidy screening of blastocysts in clinical preimplantation genetic screening cyclesSemantic proximity Read ↗

An overview of the current and emerging platforms for preimplantation genetic testing for aneuploidies (PGT-A) in in vitro fertilization programsSemantic proximity Read ↗

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