Demonstration venue · read-only. Every page can be browsed; the buttons that would change it are switched off. Create an account to run TaxoReview on your own data. A simulation from public publication records: the people listed were not invited and did not agree to review.
? Tutorial for this page

Jason R. Grant

dblp:65/7244 · DBLP profile ↗
← Back
2ranked-venue papers
1as first author
0since 2021 · last 2019
0000-0002-0407-9807ORCID · conflict

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 2 · 1 first-author

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 100%

Topics — the 3 heaviest of 3, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
genomics
0.112011
In-depth annotation of SNPs arising from resequencing projects using NGS-SNP · Bioinform. 2011
Bioinformatics and computational biology › genomics › variant annotation
SNP annotation
0.112011
In-depth annotation of SNPs arising from resequencing projects using NGS-SNP · Bioinform. 2011
Bioinformatics and computational biology › genomics › variant annotation
SNP functional annotation
0.112011
In-depth annotation of SNPs arising from resequencing projects using NGS-SNP · Bioinform. 2011

Methods — techniques the papers use, named apart from their topics

orthologous sequence comparison · 0.1
YearPublicationVenuePosition
2019 Visualizing and comparing circular genomes using the CGView family of tools
abstract
Graphical genome maps are widely used to assess genome features and sequence characteristics. The CGView (Circular Genome Viewer) software family is a popular collection of tools for generating genome maps for bacteria, organelles and viruses. In this review, we describe the capabilities of the original CGView program along with those of subsequent companion applications, including the CGView Server and the CGView Comparison Tool. We also discuss GView, a graphical user interface-enabled rewrite of CGView, and the GView Server, which offers several integrated analyses for identifying shared or unique genome regions relative to a collection of comparison genomes. We conclude with some remarks about our current development efforts related to CGView aimed at adding new functionality while increasing ease of use.
Paul Stothard, Jason R. Grant, Gary H. Van Domselaar
Briefings Bioinform.2
2011 In-depth annotation of SNPs arising from resequencing projects using NGS-SNP
abstract
SUMMARY: NGS-SNP is a collection of command-line scripts for providing rich annotations for SNPs identified by the sequencing of whole genomes from any organism with reference sequences in Ensembl. Included among the annotations, several of which are not available from any existing SNP annotation tools, are the results of detailed comparisons with orthologous sequences. These comparisons can, for example, identify SNPs that affect conserved residues, or alter residues or genes linked to phenotypes in another species. AVAILABILITY: NGS-SNP is available both as a set of scripts and as a virtual machine. The virtual machine consists of a Linux operating system with all the NGS-SNP dependencies pre-installed. The source code and virtual machine are freely available for download at http://stothard.afns.ualberta.ca/downloads/NGS-SNP/. CONTACT: [email protected] SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Jason R. Grant, Adriano S. Arantes, Xiaoping Liao, Paul Stothard
Bioinform.1