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

NGS_SNPAnalyzer: a desktop software supporting genome projects by identifying and visualizing sequence variations from next-generation sequencing data.

Genes & genomics - 1 Nov 2020

Lee Dong-Jun, Kwon Taesoo, Kim Chang-Kug, Seol Young-Joo, Park Dong-Suk, Lee Tae-Ho, Ahn Byung-Ohg

Abstract excerpt

BACKGROUND: Sequence variations such as single nucleotide polymorphisms are markers for genetic diseases and breeding. Therefore, identifying sequence variations is one of the main objectives of several genome projects. Although most genome project consortiums provide standard operation procedures for sequence variation detection methods, there may be differences in the results because of human selection or...

Read the complete abstract on PubMed

Topics

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

Share to Breeding
Share to Computational Biology

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Diseases, Inborn

Share to High-Throughput Nucleotide Sequencing

Share to Polymorphism, Single Nucleotide

Share to Sequence Analysis, DNA

Share to Software

Source

Open in PubMed Open full text

Identifiers

PMID: 32980993
DOI: 10.1007/s13258-020-00997-7
PMCID: PMC7567733

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

NGS_SNPAnalyzer: a desktop software supporting genome projects by identifying and visualizing sequence variations from next-generation sequencing data.PMID 32980993Read ↗

NGSpop: A desktop software that supports population studies by identifying sequence variations from next-generation sequencing dataSemantic proximity Read ↗

SNVerGUI: a desktop tool for variant analysis of next-generation sequencing data.Semantic proximity Read ↗

An integrated SNP mining and utilization (ISMU) pipeline for next generation sequencing data.Semantic proximity Read ↗

NGS for Sequence Variants.Semantic proximity Read ↗

VisVariant: A java program to visualise genetic variants in next-generation sequencing dataSemantic proximity Read ↗

SNPHunter: a versatile web-based tool for acquiring and managing single nucleotide polymorphisms.Semantic proximity Read ↗

MagicViewer: integrated solution for next-generation sequencing data visualization and genetic variation detection and annotation.Semantic proximity Read ↗

DNAscan2: a versatile, scalable, and user-friendly analysis pipeline for next-generation sequencing dataSemantic proximity Read ↗

A beginners guide to SNP calling from high-throughput DNA-sequencing data.Semantic proximity Read ↗

QualitySNPng: a user-friendly SNP detection and visualization tool.Semantic proximity Read ↗

SNPAnalyzer: a web-based integrated workbench for single-nucleotide polymorphism analysis.Semantic proximity Read ↗

A survey of tools for variant analysis of next-generation genome sequencing data.Semantic proximity Read ↗

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