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 gel-free SNP genotyping method: bioluminometric assay coupled with modified primer extension reactions (BAMPER) directly from double-stranded PCR products.

Human mutation - 1 Aug 2004

Zhou Guo-Hua, Shirakura Hiromi, Kamahori Masao, Okano Kazunori, Nagai Keiichi, Kambara Hideki

Abstract excerpt

Inexpensive, high-throughput genotyping methods are needed for analyzing human genetic variations. We have successfully applied the regular bioluminometric assay coupled with modified primer extension reactions (BAMPER) method to single-nucleotide polymorphism (SNP) typing as well as the allele frequency determination for various SNPs. This method includes the production of single-strand target DNA from a genome...

Read the complete abstract on PubMed

Topics

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

Share to Base Pair Mismatch
Share to Diphosphates

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA Primers

Share to Genome

Share to Luminescent Measurements

Share to Myocardium

Share to Nucleic Acid Amplification Techniques

Source

Identifiers

PMID: 15241797
DOI: 10.1002/humu.20052

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

A gel-free SNP genotyping method: bioluminometric assay coupled with modified primer extension reactions (BAMPER) directly from double-stranded PCR products.PMID 15241797Read ↗

Quantitative detection of single nucleotide polymorphisms for a pooled sample by a bioluminometric assay coupled with modified primer extension reactions (BAMPER).Semantic proximity Read ↗

Single-nucleotide polymorphism typing based on pyrosequencing chemistry and acryl-modified glass chip.Semantic proximity Read ↗

Development of bioluminescent pyrophosphate assay using pyruvate phosphate dikinase and its application to single-nucleotide polymorphism analysis.Semantic proximity Read ↗

Multiplex SNP typing by bioluminometric assay coupled with terminator incorporation (BATI).Semantic proximity Read ↗

Quantitative analysis of single-nucleotide polymorphisms by pyrosequencing with di-base addition.Semantic proximity Read ↗

Single nucleotide polymorphism analysis by allele-specific primer extension with real-time bioluminescence detection in a microfluidic device.Semantic proximity Read ↗

A multiplexing single nucleotide polymorphism typing method based on restriction-enzyme-mediated single-base extension and capillary electrophoresis.Semantic proximity Read ↗

Pyrosequencing for SNP genotyping.Semantic proximity Read ↗

Enhanced discrimination of single nucleotide polymorphism in genotyping by phosphorothioate proofreading allele-specific amplification.Semantic proximity Read ↗

Detection of multiple SNPs in numerous samples with polyacrylamide gel-based microarray.Semantic proximity Read ↗

Pyrosequencing: an accurate detection platform for single nucleotide polymorphisms.Semantic proximity Read ↗

DNAzyme based gap-LCR detection of single-nucleotide polymorphism.Semantic proximity Read ↗

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