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Article

Studying copy number variations using a nanofluidic platform.

Nucleic acids research - 1 Oct 2008

Qin Jian, Jones Robert C, Ramakrishnan Ramesh

Abstract excerpt

Copy number variations (CNVs) in the human genome are conventionally detected using high-throughput scanning technologies, such as comparative genomic hybridization and high-density single nucleotide polymorphism (SNP) microarrays, or relatively low-throughput techniques, such as quantitative polymerase chain reaction (PCR). All these approaches are limited in resolution and can at best distinguish a twofold (or...

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PMID: 18710881
DOI: 10.1093/nar/gkn518
PMCID: PMC2566873

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ERBB2

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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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