Copy Number Variation (cnv) Analysis: - Cancer Science

Relevant Publications

[Genetic analysis of a fetus with with 45,X/46,X,idic(Y)(q11.2) mosaicism].

Issue Release: 2024

Analysis of genomic copy number variations through whole-genome scan in Yunling cattle.

Issue Release: 2024

Correlation between maternal serum biomarkers and the risk of fetal chromosome copy number variants: a single-center retrospective study.

Issue Release: 2024

A computational pipeline for identifying gene targets and signalling pathways in cancer cells to improve lymphocyte infiltration and immune checkpoint therapy efficacy.

Issue Release: 2024

Radiogenomics Map-Based Molecular and Imaging Phenotypical Characterization in Localised Prostate Cancer Using Pre-Biopsy Biparametric MR Imaging.

Issue Release: 2024

Droplet Hi-C for Fast and Scalable Profiling of Chromatin Architecture in Single Cells.

Issue Release: 2024

Whole-exome sequencing-based mutational profiling of hepatocellular adenoma malignant transformation to hepatocellular carcinoma.

Issue Release: 2024

Genetic Testing for Global Developmental Delay in Early Childhood.

Issue Release: 2024

[Genetic analysis of the false positive trisomy 7 and false negative trisomy 18 by NIPT-PLUS].

Issue Release: 2024

Identification of the genetic characteristics of copy number variations in experimental specific pathogen-free ducks using whole-genome resequencing.

Issue Release: 2024

Use of the MS-MLPA assay in prenatal diagnosis of Prader-Willi syndrome with mosaic trisomy 15.

Issue Release: 2024

Natural history of germline BRCA1 mutated and BRCA wild-type triple-negative breast cancer.

Issue Release: 2024

Clinical value of positive CNVs results by NIPT without fetal ultrasonography-identified structural anomalies.

Issue Release: 2024

A Burden of Rare Copy Number Variants in Obsessive-Compulsive Disorder.

Issue Release: 2024

The potential of liquid biopsy for detection of the KIAA1549-BRAF fusion in circulating tumor DNA from children with pilocytic astrocytoma.

Issue Release: 2024

Optimized MLPA workflow for spinal muscular atrophy diagnosis: identification of a novel variant, NC_000005.10:g.(70919941_70927324)del in isolated exon 1 of SMN1 gene through long-range PCR.

Issue Release: 2024

Identification and validation of a novel anoikis-related prognostic model for prostate cancer.

Issue Release: 2024

Differential whole-genome doubling based signatures for improvement on clinical outcomes and drug response in patients with breast cancer.

Issue Release: 2024

Appropriate whole genome amplification and pathogenic loci detection can improve the accuracy of preimplantation genetic diagnosis for deletional α-thalassemia.

Issue Release: 2024

OSCAA: A two-dimensional Gaussian mixture model for copy number variation association analysis.

Issue Release: 2024

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