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Nicole T. Perna

dblp:p/NicoleTPerna · DBLP profile ↗
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4ranked-venue papers
0as first author
0since 2021 · last 2009
0000-0001-8208-0929ORCID · verified

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

Applied, interdisciplinary, general and emerging computing · 4

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
2 papers
Bioinformatics and computational biology · 100%

Topics — the 6 heaviest of 6, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › sequence alignment
genome alignment
0.112009
Reordering contigs of draft genomes using the Mauve Aligner · Bioinform. 2009
Bioinformatics and computational biology › sequence analysis › sequence assembly
genome assembly
0.112009
Reordering contigs of draft genomes using the Mauve Aligner · Bioinform. 2009
Bioinformatics and computational biology
comparative genomics
0.012004
GRIL: genome rearrangement and inversion locator · Bioinform. 2004
Bioinformatics and computational biology › comparative genomics
genome rearrangement
0.012004
GRIL: genome rearrangement and inversion locator · Bioinform. 2004
Bioinformatics and computational biology › sequence alignment › genome alignment
multiple genome alignment
0.012004
GRIL: genome rearrangement and inversion locator · Bioinform. 2004
Bioinformatics and computational biology
sequence analysis
0.012004
GRIL: genome rearrangement and inversion locator · Bioinform. 2004

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

collinearity detection · 0.0
YearPublicationVenuePosition
2009 Reordering contigs of draft genomes using the Mauve Aligner
abstract
Abstract Summary: Mauve Contig Mover provides a new method for proposing the relative order of contigs that make up a draft genome based on comparison to a complete or draft reference genome. A novel application of the Mauve aligner and viewer provides an automated reordering algorithm coupled with a powerful drill-down display allowing detailed exploration of results. Availability: The software is available for download at http://gel.ahabs.wisc.edu/mauve. Contact: [email protected] Supplementary information: Supplementary data are available at Bioinformatics online and http://gel.ahabs.wisc.edu
Anna I. Rissman, Bob Mau, Bryan S. Biehl, Aaron E. Darling, Jeremy D. Glasner, Nicole T. Perna
Bioinform.6
2009 Text-mining of PubMed abstracts by natural language processing to create a public knowledge base on molecular mechanisms of bacterial enteropathogens
abstract
BACKGROUND: The Enteropathogen Resource Integration Center (ERIC; http://www.ericbrc.org) has a goal of providing bioinformatics support for the scientific community researching enteropathogenic bacteria such as Escherichia coli and Salmonella spp. Rapid and accurate identification of experimental conclusions from the scientific literature is critical to support research in this field. Natural Language Processing (NLP), and in particular Information Extraction (IE) technology, can be a significant aid to this process. DESCRIPTION: We have trained a powerful, state-of-the-art IE technology on a corpus of abstracts from the microbial literature in PubMed to automatically identify and categorize biologically relevant entities and predicative relations. These relations include: Genes/Gene Products and their Roles; Gene Mutations and the resulting Phenotypes; and Organisms and their associated Pathogenicity. Evaluations on blind datasets show an F-measure average of greater than 90% for entities (genes, operons, etc.) and over 70% for relations (gene/gene product to role, etc). This IE capability, combined with text indexing and relational database technologies, constitute the core of our recently deployed text mining application. CONCLUSION: Our Text Mining application is available online on the ERIC website (http://www.ericbrc.org/portal/eric/articles). The information retrieval interface displays a list of recently published enteropathogen literature abstracts, and also provides a search interface to execute custom queries by keyword, date range, etc. Upon selection, processed abstracts and the entities and relations extracted from them are retrieved from a relational database and marked up to highlight the entities and relations. The abstract also provides links from extracted genes and gene products to the ERIC Annotations database, thus providing access to comprehensive genomic annotations and adding value to both the text-mining and annotations systems.
Sam Zaremba, Mila Ramos-Santacruz, Thomas Hampton, Panna Shetty, Joel Fedorko, Jon Whitmore, John M. Greene, Nicole T. Perna, Jeremy D. Glasner, Guy Plunkett III, Matthew Shaker, David Pot
BMC Bioinform.8
2006 Procrastination Leads to Efficient Filtration for Local Multiple Alignment
Aaron E. Darling, Todd J. Treangen, Louxin Zhang, Carla Kuiken, Xavier Messeguer, Nicole T. Perna
WABI6
2004 GRIL: genome rearrangement and inversion locator
abstract
Abstract Summary: GRIL is a tool to automatically identify collinear regions in a set of bacterial-size genome sequences. GRIL uses three basic steps. First, regions of high sequence identity are located. Second, some of these regions are filtered based on user-specified criteria. Finally, the remaining regions of sequence identity are used to define significant collinear regions among the sequences. By locating collinear regions of sequence, GRIL provides a basis for multiple genome alignment using current alignment systems. GRIL also provides a basis for using current inversion distance tools to infer phylogeny. Availability: GRIL is implemented in C++ and runs on any x86-based Linux or Windows platform. It is available from http://asap.ahabs.wisc.edu/gril Supplementary information: The GRIL web site contains a detailed description of the GRIL's algorithms, an example of applying GRIL to five genomes, and verification of the correctness of the results.
Aaron E. Darling, Bob Mau, Frederick R. Blattner, Nicole T. Perna
Bioinform.4