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

Clinical laboratory implementation of cytogenomic microarrays.

Cytogenetic and genome research - 1 Jan 2011

South S T, Brothman A R

Abstract excerpt

Examination of the whole genome for copy number alterations by microarray is now routinely done in many laboratories. The field of cytogenetics has evolved to adapt this technology, and the current phase of transition has resulted in the need for standardization in methodologies and interpretation of data. This review will outline some of the changes addressed in the field over the last several years and briefly...

Read the complete abstract on PubMed

Topics

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

Share to Comparative Genomic Hybridization
Share to Cytogenetic Analysis
Share to Data Interpretation, Statistical

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA Copy Number Variations

Share to Gene Dosage

Share to Oligonucleotide Array Sequence Analysis

Share to Reproducibility of Results

Share to Software

Source

Identifiers

PMID: 21934287
DOI: 10.1159/000331425

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.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Clinical laboratory implementation of cytogenomic microarrays.PMID 21934287Read ↗

Clinical application of microarray-based molecular cytogenetics: an emerging new era of genomic medicine.Semantic proximity Read ↗

Guidelines for genomic array analysis in acquired haematological neoplastic disordersSemantic proximity Read ↗

Types of array findings detectable in cytogenetic diagnosis: a proposal for a generic classificationSemantic proximity Read ↗

Detection of Chromosomal Aberrations in Clinical Practice: From Karyotype to Genome SequenceSemantic proximity Read ↗

Integration of microarray analysis into the clinical diagnosis of hematological malignancies: How much can we improve cytogenetic testing?Semantic proximity Read ↗

Clinical use of SNP-microarrays for the detection of genome-wide changes in haematological malignanciesSemantic proximity Read ↗

DNA microarrays in medical practice.Semantic proximity Read ↗

Microarray-based DNA profiling to study genomic aberrations.Semantic proximity Read ↗

Genome-wide arrays in routine diagnostics of hematological malignancies.Semantic proximity Read ↗

American College of Medical Genetics and Genomics technical standards and guidelines: microarray analysis for chromosome abnormalities in neoplastic disordersSemantic proximity Read ↗

Genomic microarrays in the spotlight.Semantic proximity Read ↗

Development and validation of a CGH microarray for clinical cytogenetic diagnosisSemantic proximity Read ↗

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