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Andrew M. Taverner

dblp:183/4448 · DBLP profile ↗
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1ranked-venue papers
0as first author
0since 2021 · last 2016
—ORCID · unresolved

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

Applied, interdisciplinary, general and emerging computing · 1

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 › population genetics › population parameter estimation
allele frequency estimation
0.212016
Ferret: a user-friendly Java tool to extract data from the 1000 Genomes Project · Bioinform. 2016
Bioinformatics and computational biology › population genetics
human genetic variation
0.212016
Ferret: a user-friendly Java tool to extract data from the 1000 Genomes Project · Bioinform. 2016
Bioinformatics and computational biology
population genetics
0.212016
Ferret: a user-friendly Java tool to extract data from the 1000 Genomes Project · Bioinform. 2016

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

data conversion · 0.2
YearPublicationVenuePosition
2016 Ferret: a user-friendly Java tool to extract data from the 1000 Genomes Project
abstract
UNLABELLED: The 1000 Genomes (1KG) Project provides a near-comprehensive resource on human genetic variation in worldwide reference populations. 1KG variants can be accessed through a browser and through the raw and annotated data that are regularly released on an ftp server. We developed Ferret, a user-friendly Java tool, to easily extract genetic variation information from these large and complex data files. From a locus, gene(s) or SNP(s) of interest, Ferret retrieves genotype data for 1KG SNPs and indels, and computes allelic frequencies for 1KG populations and optionally, for the Exome Sequencing Project populations. By converting the 1KG data into files that can be imported into popular pre-existing tools (e.g. PLINK and HaploView), Ferret offers a straightforward way, even for non-bioinformatics specialists, to manipulate, explore and merge 1KG data with the user's dataset, as well as visualize linkage disequilibrium pattern, infer haplotypes and design tagSNPs. AVAILABILITY AND IMPLEMENTATION: Ferret tool and source code are publicly available at http://limousophie35.github.io/Ferret/ CONTACT: [email protected] SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Sophie Limou, Andrew M. Taverner, Cheryl A. Winkler
Bioinform.2