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

Mutation surveyor: an in silico tool for sequencing analysis.

Methods in molecular biology (Clifton, N.J.) - 1 Jan 2011

Dong Chongmei, Yu Bing

Abstract excerpt

DNA sequencing is widely used for DNA diagnostics and functional studies of genes of interest. With significantly increased sequencing outputs, manual reading of sequence results can impede an efficient and accurate analysis. Mutation Surveyor is a useful in silico tool developed by SoftGenetics that assists the detection of sequence variations within Sanger sequencing traces. This tool can process up to 400...

Read the complete abstract on PubMed

Topics

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

Share to Databases, Genetic
Share to Plant Proteins
Share to Polymorphism, Single Nucleotide

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Receptors, LDL

Share to Sequence Analysis

Share to Software

Share to Starch Synthase

Share to Triticum

Source

Identifiers

PMID: 21780000
DOI: 10.1007/978-1-61779-176-5_14

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Mutation surveyor: an in silico tool for sequencing analysis.PMID 21780000Read ↗

Mutation surveyor: software for DNA sequence analysis.Semantic proximity Read ↗

Mutation and polymorphism detection: a technical overview.Semantic proximity Read ↗

GLASS: assisted and standardized assessment of gene variations from Sanger sequence trace dataSemantic proximity Read ↗

DAJIN enables multiplex genotyping to simultaneously validate intended and unintended target genome editing outcomes.Semantic proximity Read ↗

MosaicSim: A Novel Mosaic Variant Simulator Reveals Diminishing Returns of Ultra-High Coverage for Mosaic Variant DetectionSemantic proximity Read ↗

MutAid: Sanger and NGS Based Integrated Pipeline for Mutation Identification, Validation and Annotation in Human Molecular Genetics.Semantic proximity Read ↗

Surveyor nuclease-based genotyping of SNPs.Semantic proximity Read ↗

Genomics: Mutator catalogues.Semantic proximity Read ↗

Rapid and efficient human mutation detection using a bench-top next-generation DNA sequencer.Semantic proximity Read ↗

MutScan: fast detection and visualization of target mutations by scanning FASTQ data.Semantic proximity Read ↗

Targeted single molecule mutation detection with massively parallel sequencing.Semantic proximity Read ↗

InSNP: a tool for automated detection and visualization of SNPs and InDels.Semantic proximity Read ↗

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