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

A genome-wide high-resolution array-CGH analysis of cutaneous melanoma and comparison of array-CGH to FISH in diagnostic evaluation.

The Journal of molecular diagnostics : JMD - 1 Sept 2013

Wang Lu, Rao Mamta, Fang Yuqiang, Hameed Meera, Viale Agnes, Busam Klaus, Jhanwar Suresh C

Abstract excerpt

Benign melanocytic nevi and cutaneous melanomas can be difficult to differentiate by means of routine microscopic analysis. Recent evidence has suggested that cytogenomic analysis may be a useful diagnostic method for evaluation of melanocytic proliferations. We investigated the array-based comparative genomic hybridization (aCGH) platform for DNA copy number analysis of formalin-fixed, paraffin-embedded (FFPE)...

Read the complete abstract on PubMed

Topics

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

Share to Algorithms
Share to Comparative Genomic Hybridization

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genome-Wide Association Study

Share to In Situ Hybridization, Fluorescence

Share to Melanoma

Share to Melanoma, Cutaneous Malignant

Share to Sensitivity and Specificity

Share to Skin Neoplasms

Source

Identifiers

PMID: 23800576
DOI: 10.1016/j.jmoldx.2013.04.001

Genes

CCND1
MYB

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A genome-wide high-resolution array-CGH analysis of cutaneous melanoma and comparison of array-CGH to FISH in diagnostic evaluation.PMID 23800576Read ↗

Copy number variation in archival melanoma biopsies versus benign melanocytic lesions.Semantic proximity Read ↗

A Highly Specific and Discriminatory FISH Assay for Distinguishing Between Benign and Malignant Melanocytic NeoplasmsSemantic proximity Read ↗

FISH as an effective diagnostic tool for the management of challenging melanocytic lesions.Semantic proximity Read ↗

Detection of Copy Number Alterations in Metastatic Melanoma by a DNA FluorescenceIn situHybridization Probe Panel and Array Comparative Genomic Hybridization: A Southwest Oncology Group Study (S9431)Semantic proximity Read ↗

Copy Number Analysis in Congenital Nevi: Concordance and Diagnostic Limitations of aCGH, sWGS, and Methylation ProfilingSemantic proximity Read ↗

DNA copy number changes correlate with clinical behavior in melanocytic neoplasms: proposal of an algorithmic approach.Semantic proximity Read ↗

Somatic alterations in the melanoma genome: a high-resolution array-based comparative genomic hybridization study.Semantic proximity Read ↗

Melanocytic nevi with an atypical epithelioid cell component: clinical, histopathologic, and fluorescence in situ hybridization findings.Semantic proximity Read ↗

Genomic profiling of malignant melanoma using tiling-resolution arrayCGH.Semantic proximity Read ↗

Detection of copy number variations in melanocytic lesions utilising array based comparative genomic hybridisationSemantic proximity Read ↗

The extent of whole-genome copy number alterations predicts aggressive features in primary melanomas.Semantic proximity Read ↗

Distinct Genomic Patterns in Pigmented Epithelioid MelanocytomaSemantic proximity Read ↗

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