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

Single-Nucleotide Polymorphism Analysis to Select Conserved Regions for an Improved Real-Time Reverse Transcription-PCR Test Specific for Newcastle Disease Virus.

Avian diseases - 1 Dec 2019

Ferreira H L, Suarez D L

Abstract excerpt

A bioinformatics approach using single-nucleotide polymorphism (SNP) analysis was performed to improve the current real-time reverse transcription-PCR (RRT-PCR) tests for the rapid detection of Newcastle disease virus (NDV). In total, 422 NDV complete genomes were analyzed using the Virus Pathogen Resource to compare the conservation of the primer and probe sequences and to select regions to develop new RRT-PCR...

Read the complete abstract on PubMed

Topics

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

Share to Chickens
Share to Genome, Viral
Share to Newcastle Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Newcastle disease virus

Share to Poultry Diseases

Share to Real-Time Polymerase Chain Reaction

Share to Sensitivity and Specificity

Share to Viral Proteins

Source

Identifiers

PMID: 31865677
DOI: 10.1637/aviandiseases-D-19-00071

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

Single-Nucleotide Polymorphism Analysis to Select Conserved Regions for an Improved Real-Time Reverse Transcription-PCR Test Specific for Newcastle Disease Virus.PMID 31865677Read ↗

High-sensitivity multiplex real-time RT-PCR for universal detection and virulence typing of Newcastle disease virus in poultry field samples.Semantic proximity Read ↗

Detection of a Broad Range of Class I and II Newcastle Disease Viruses Using a Multiplex Real-Time Reverse Transcription Polymerase Chain Reaction AssaySemantic proximity Read ↗

False-Negative Results of a Validated Real-Time PCR Protocol for Diagnosis of Newcastle Disease Due to Genetic Variability of the Matrix GeneSemantic proximity Read ↗

Detection of Newcastle disease virus using nucleic acid sequence-based amplification.Semantic proximity Read ↗

Newcastle disease: evolution of genotypes and the related diagnostic challenges.Semantic proximity Read ↗

Establishment of reverse transcription recombinase–aided amplification-lateral-flow dipstick and real-time fluorescence–based reverse transcription recombinase–aided amplification methods for detection of the Newcastle disease virus in chickensSemantic proximity Read ↗

Application of whole genome data for in silico evaluation of primers and probes routinely employed for the detection of viral species by RT-qPCR using dengue virus as a case studySemantic proximity Read ↗

The Development of Novel Reverse Transcription Loop-Mediated Isothermal Amplification Assays for the Detection and Differentiation of Virulent Newcastle Disease VirusSemantic proximity Read ↗

Newcastle disease: progress and gaps in the development of vaccines and diagnostic tools.Semantic proximity Read ↗

Use of mutational pattern in 5'-NCR and VP1 regions of polioviruses for molecular diagnosis.Semantic proximity Read ↗

Molecular epidemiology of Newcastle disease in Republic of KoreaSemantic proximity Read ↗

Development of a real-time reverse-transcription PCR for the detection and simultaneous pathotyping of Newcastle disease virus isolates using a novel probeSemantic proximity Read ↗

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