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Article

Semiconductor Sequencing Analysis of Chromosomal Copy Number Variations in Spontaneous Miscarriage.

Medical science monitor : international medical journal of experimental and clinical research - 22 Nov 2017

Wang Ming-Zhu, Lin Fang-Qin, Li Min, He Dan, Yu Qi-Hong, Yang Xue-Xi, Wu Ying-Song

Abstract excerpt

BACKGROUND Array CGH is the criterion standard for identifying copy number variations (CNV), but the restrictive requirement of DNA quality and relatively high cost prevent the use of this method as a general assay in hospitals in developing countries. Our principal objective was to determine whether the semiconductor sequencing platform (SSP) could be an alternative method in CNV detection for spontaneous...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 29162795
DOI: 10.12659/msm.905094
PMCID: PMC5707912

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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