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

Variability in interpreting and reporting copy number changes detected by array-based technology in clinical laboratories

1 Dec 2009

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 Genomic variations and chromosomal abnormalities
Share to Genomics and Rare Diseases
Share to Prenatal Screening and Diagnostics

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 19904209
DOI: 10.1097/gim.0b013e3181c0c3b0

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Variability in interpreting and reporting copy number changes detected by array-based technology in clinical laboratoriesPMID 19904209Read ↗

Practical guidelines for interpreting copy number gains detected by high-resolution array in routine diagnosticsSemantic proximity Read ↗

Standardization and diversification of copy number microarray testing for clinical diagnostics--implications of the cross-platform/algorithm study on clinical diagnostic chromosomal microarray analysis.Semantic proximity Read ↗

A pilot study to investigate the clinically predictive values of copy number variations detected by next-generation sequencing of cell-free deoxyribonucleic acid in spent culture mediaSemantic proximity Read ↗

Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants.Semantic proximity Read ↗

Copy Number Variation in Common DiseaseSemantic proximity Read ↗

Microarray Techniques to Analyze Copy-Number Alterations in Genomic DNA: Array Comparative Genomic Hybridization and Single-Nucleotide Polymorphism Array.Semantic proximity Read ↗

Performance assessment of copy number microarray platforms using a spike-in experiment.Semantic proximity Read ↗

Clinical laboratory implementation of cytogenomic microarrays.Semantic proximity Read ↗

Detection of DNA copy number alterations in cancer by array comparative genomic hybridizationSemantic proximity Read ↗

The impact of errors in copy number variation detection algorithms on association results.Semantic proximity Read ↗

Diagnostic utility of array-based Comparative Genomic Hybridization in a clinical settingSemantic proximity Read ↗

Comparing CNV detection methods for SNP arrays.Semantic proximity Read ↗

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