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

Evaluation of nanofluidics technology for high-throughput SNP genotyping in a clinical setting.

The Journal of molecular diagnostics : JMD - 1 May 2011

Chan Maurice, Chan Mei Wen, Loh Ting Wei, Law Hai Yang, Yoon Chui Sheun, Than Sint Sint, Chua Jia Mei, Wong Chow Yin, Yong Wei Sean, Yap Yoon Sim, Ho Gay Hui, Ang Peter, Lee Ann Siew Gek

Abstract excerpt

The current need for high-throughput genotyping platforms for targeted validation of disease-associated single nucleotide polymorphisms (SNPs) motivated us to evaluate a novel nanofluidics platform for genotyping DNA extracted from peripheral blood and buccal wash samples. SNP genotyping was performed using a Fluidigm 48.48 Dynamic Array biochip on the BioMark polymerase chain reaction platform and results were...

Read the complete abstract on PubMed

Topics

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

Share to High-Throughput Screening Assays
Share to Microfluidic Analytical Techniques

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Molecular Typing

Share to Polymorphism, Single Nucleotide

Share to Reproducibility of Results

Share to Sensitivity and Specificity

Source

Open in PubMed Open full text

Identifiers

PMID: 21497291
DOI: 10.1016/j.jmoldx.2010.12.001
PMCID: PMC3077727

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

Evaluation of nanofluidics technology for high-throughput SNP genotyping in a clinical setting.PMID 21497291Read ↗

High-throughput single nucleotide polymorphism genotyping using nanofluidic Dynamic Arrays.Semantic proximity Read ↗

A nanoliter fluidic platform for large-scale single nucleotide polymorphism genotyping.Semantic proximity Read ↗

Genotyping technologies for genetic research.Semantic proximity Read ↗

Microelectronic array system for molecular diagnostic genotyping: Nanogen NanoChip 400 and molecular biology workstation.Semantic proximity Read ↗

Nanofluidic Allele-Specific Digital PCR Method for Quantifying IDH1 and IDH2 Mutation Burden in Acute Myeloid Leukemia.Semantic proximity Read ↗

A nanobiotechnology roadmap for high-throughput single nucleotide polymorphism analysis.Semantic proximity Read ↗

Microfluidic genotyping by rapid serial PCR and high-speed melting analysis.Semantic proximity Read ↗

Ultra-fast sample-to-sequencing workflow for clinical diagnostics using micropillarsSemantic proximity Read ↗

The effect of input DNA copy number on genotype call and characterising SNP markers in the humpback whale genome using a nanofluidic array.Semantic proximity Read ↗

SalivaSense 2.0: Multiplex cfDNA‑cfRNA Epigenome Signatures Enabling Pico‑Stage Oral Squamous Cell Carcinoma Detection, Validation Frameworks and Translational PipelinesSemantic proximity Read ↗

Microfluidic droplet enrichment for targeted sequencing.Semantic proximity Read ↗

Revolutionising High Resolution HLA Genotyping for Transplant Assessment: Validation, Implementation and Challenges of Oxford Nanopore Technologies' Q20+ Sequencing.Semantic proximity Read ↗

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