Junghwan Baek

dblp:177/9226 · DBLP profile ↗
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1ranked-venue papers
1as first author
0since 2021 · last 2018
—ORCID · none

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

Applied, interdisciplinary, general and emerging computing · 1 · 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 › transcriptomics › non-coding RNA analysis
long non-coding RNA identification
0.312018
LncRNAnet: long non-coding RNA identification using deep learning · Bioinform. 2018
Bioinformatics and computational biology › sequence analysis
non-coding RNA identification
0.312018
LncRNAnet: long non-coding RNA identification using deep learning · Bioinform. 2018
Bioinformatics and computational biology › sequence analysis
RNA sequence analysis
0.112018
LncRNAnet: long non-coding RNA identification using deep learning · Bioinform. 2018

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

recurrent neural network · 0.3deep learning · 0.3convolutional neural network · 0.3
YearPublicationVenuePosition
2018 LncRNAnet: long non-coding RNA identification using deep learning
abstract
Motivation: Long non-coding RNAs (lncRNAs) are important regulatory elements in biological processes. LncRNAs share similar sequence characteristics with messenger RNAs, but they play completely different roles, thus providing novel insights for biological studies. The development of next-generation sequencing has helped in the discovery of lncRNA transcripts. However, the experimental verification of numerous transcriptomes is time consuming and costly. To alleviate these issues, a computational approach is needed to distinguish lncRNAs from the transcriptomes. Results: We present a deep learning-based approach, lncRNAnet, to identify lncRNAs that incorporates recurrent neural networks for RNA sequence modeling and convolutional neural networks for detecting stop codons to obtain an open reading frame indicator. lncRNAnet performed clearly better than the other tools for sequences of short lengths, on which most lncRNAs are distributed. In addition, lncRNAnet successfully learned features and showed 7.83%, 5.76%, 5.30% and 3.78% improvements over the alternatives on a human test set in terms of specificity, accuracy, F1-score and area under the curve, respectively. Availability and implementation: Data and codes are available in http://data.snu.ac.kr/pub/lncRNAnet.
Junghwan Baek, Byunghan Lee, Sunyoung Kwon, Sungroh Yoon
Bioinform.1