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Chun-Hway Hsueh

dblp:136/2597 · DBLP profile ↗
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1ranked-venue papers
0as first author
0since 2021 · last 2013
0000-0002-6477-7148ORCID · verified

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
genome annotation
0.212013
PRAP: an ab initio software package for automated genome-wide analysis of DNA repeats for prokaryotes · Bioinform. 2013
Bioinformatics and computational biology › genomics › microbial genomics
prokaryotic genomics
0.012013
PRAP: an ab initio software package for automated genome-wide analysis of DNA repeats for prokaryotes · Bioinform. 2013

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

de novo repeat finding · 0.2
YearPublicationVenuePosition
2013 PRAP: an ab initio software package for automated genome-wide analysis of DNA repeats for prokaryotes
abstract
MOTIVATION: Prokaryotic genome annotation has been focused mainly on identifying all genes and their protein functions. However, <30% of the prokaryotic genomes submitted to GenBank contain partial repeat features of specific types and none of the genomes contain complete repeat annotations. Deciphering all repeats in DNA sequences is an important and open task in genome annotation and bioinformatics. Hence, there is an immediate need of a tool capable of identifying full spectrum repeats in the whole genome. RESULTS: We report the PRAP (Prokaryotic Repeats Annotation Program software package to automate the analysis of repeats in both finished and draft genomes. It is aimed at identifying full spectrum repeats at the scale of the prokaryotic genome. Compared with the major existing repeat finding tools, PRAP exhibits competitive or better results. The results are consistent with manually curated and experimental data. Repeats can be identified and grouped into families to define their relevant types. The final output is parsed into the European Molecular Biology Laboratory (EMBL)/GenBank feature table format for reading and displaying in Artemis, where it can be combined or compared with other genome data. It is currently the most complete repeat finder for prokaryotes and is a valuable tool for genome annotation. AVAILABILITY: https://sites.google.com/site/prapsoftware/ CONTACT: [email protected]. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Gwo-Liang Chen, Yun-Juan Chang, Chun-Hway Hsueh
Bioinform.3