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

High-throughput genotyping system as a robust and useful tool in oncology: experience from a single institution.

Biologicals : journal of the International Association of Biological Standardization - 1 Nov 2013

Henríquez-Hernández Luis Alberto, Valenciano Almudena, Herrera-Ramos Estefanía, Lloret Marta, Riveros-Perez Alba, Lara Pedro C

Abstract excerpt

BACKGROUND AND AIM: Single nucleotide polymorphisms (SNPs) are substitutions of one base for another in the gene sequence and conforms the basis for pharmacogenetics and the development of personalized medicine. Many methods have been developed for SNP genotyping. The aim of the present study was to validate the use of a novel high-throughput genotyping system. METHODS: Five SNPs (rs25487, rs25489, rs1799782,...

Read the complete abstract on PubMed

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Topics

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

Share to Feasibility Studies
Share to Gene Frequency
Share to Genotyping Techniques
Share to Microarray Analysis
Share to Neoplasms
Share to Outcome Assessment, Health Care
Share to Polymorphism, Restriction Fragment Length
Share to Reproducibility of Results

Source

Identifiers

PMID: 24103542
DOI: 10.1016/j.biologicals.2013.09.006

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 11 closest

High-throughput genotyping system as a robust and useful tool in oncology: experience from a single institution.PMID 24103542Read ↗

A Novel Tetra-Primer ARMS-PCR for genotyping of the OPRM 1 gene rs1779791 variant associated with opioid use disordersSemantic proximity Read ↗

Analysis of the Frequency of 10 Polymorphic Markers of CDKN2A and RB1 Genes in Russian Populations.Semantic proximity Read ↗

Biochip-Based Genotyping Assay for Detection of Polymorphisms in Pigmentation Genes Associated with Cutaneous Melanoma.Semantic proximity Read ↗

A novel tetra-primer ARMS-PCR for genotyping of the OPRM1 gene rs1799971 variant associated with opioid use disorders.Semantic proximity Read ↗

Fibroblast growth factor receptor 4 gene (FGFR4) 388Arg allele predicts prolonged survival and platinum sensitivity in advanced ovarian cancer.Semantic proximity Read ↗

Genotyping of UGT1A1*80 as an Alternative to UGT1A1*28 Genotyping in SpainSemantic proximity Read ↗

APEX microarray panel for genotyping polymorphisms in cancer chemotherapy and estimation frequencies in a Slovak population.Semantic proximity Read ↗

Setting up a probe based, closed tube real-time PCR assay for focused detection of variable sequence alterations.Semantic proximity Read ↗

Development of a rapid genotyping method for single nucleotide polymorphisms and its application in cancer studies.Semantic proximity Read ↗

Detection of single-nucleotide polymorphisms in cancer-related genes by minisequencing on a microelectronic DNA chip.Semantic proximity Read ↗

An Optimized Single Nucleotide Polymorphism-Based Detection Method Suggests That Allelic Variants in the 3’ Untranslated Region of RRAS2 Correlate with Treatment Response in Chronic Lymphocytic Leukemia PatientsSemantic proximity Read ↗

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