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

Jennifer J. Knapp

dblp:248/4779 · DBLP profile ↗
← Back
1ranked-venue papers
0as first author
0since 2021 · last 2019
—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 2 heaviest of 2, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › protein function prediction
functional impact prediction
0.412019
A web application and service for imputing and visualizing missense variant effect maps · Bioinform. 2019
Bioinformatics and computational biology › statistical genetics
variant effect prediction
0.412019
A web application and service for imputing and visualizing missense variant effect maps · Bioinform. 2019

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

imputation · 0.4
YearPublicationVenuePosition
2019 A web application and service for imputing and visualizing missense variant effect maps
abstract
SUMMARY: The promise of personalized genomic medicine depends on our ability to assess the functional impact of rare sequence variation. Multiplexed assays can experimentally measure the functional impact of missense variants on a massive scale. However, even after such assays, many missense variants remain poorly measured. Here we describe a software pipeline and application to impute missing information in experimentally determined variant effect maps. AVAILABILITY AND IMPLEMENTATION: http://impute.varianteffect.org source code: https://github.com/joewuca/imputation. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Yingzhou Wu, Jochen Weile, Atina G. Coté, Jennifer J. Knapp, Marta Verby, Frederick P. Roth
Bioinform.5