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

High resolution global chromosomal aberrations from spontaneous miscarriages revealed by low coverage whole genome sequencing

8 Mar 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 Assisted Reproductive Technology and Twin Pregnancy
Share to Genomic variations and chromosomal abnormalities
Share to Prenatal Screening and Diagnostics

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 29525519
DOI: 10.1016/j.ejogrb.2018.03.008

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

High resolution global chromosomal aberrations from spontaneous miscarriages revealed by low coverage whole genome sequencingPMID 29525519Read ↗

Genome Sequencing Explores Complexity of Chromosomal Abnormalities in Recurrent MiscarriageSemantic proximity Read ↗

The genomic basis of sporadic and recurrent pregnancy loss: a comprehensive in-depth analysis of 24,900 miscarriagesSemantic proximity Read ↗

Chromosomal Copy Number Variation Analysis in Pregnancy Products from Recurrent and Sporadic Miscarriage Using Next-Generation SequencingSemantic proximity Read ↗

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

Prevalence of chromosomal abnormalities identified by copy number variation sequencing in high-risk pregnancies, spontaneous abortions, and suspected genetic disordersSemantic proximity Read ↗

Incidence and spectrum of chromosome abnormalities in spontaneous abortions: New insights from a 12-year studySemantic proximity Read ↗

Low-pass whole-genome sequencing in clinical cytogenetics: a validated approachSemantic proximity Read ↗

A Novel System for the Detection of Spontaneous Abortion-Causing Aneuploidy and Its Erroneous Chromosome Origins through the Combination of Low-Pass Copy Number Variation Sequencing and NGS-Based STR TestsSemantic proximity Read ↗

Low-Coverage Whole Genome Sequencing Diagnoses Endometrial Carcinoma from Tampon DNA of Uterine Bleeding PatientsSemantic proximity Read ↗

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

What have studies of genomic disorders taught us about our genome?Semantic proximity Read ↗

Identification of balanced chromosomal rearrangements previously unknown among participants in the 1000 Genomes Project: implications for interpretation of structural variation in genomes and the future of clinical cytogeneticsSemantic proximity Read ↗

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