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Hyeonju Son

dblp:187/5708 · DBLP profile ↗
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2ranked-venue papers
0as 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 · 2

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

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › genomics
variant calling
0.312018
AIRVF: a filtering toolbox for precise variant calling in Ion Torrent sequencing · Bioinform. 2018
Bioinformatics and computational biology
cancer genomics
0.212016
Vecuum: identification and filtration of false somatic variants caused by recombinant vector contamination · Bioinform. 2016
Bioinformatics and computational biology › cancer genomics › somatic mutation analysis
somatic mutation detection
0.212016
Vecuum: identification and filtration of false somatic variants caused by recombinant vector contamination · Bioinform. 2016
Bioinformatics and computational biology › sequence analysis › sequencing read preprocessing
vector contamination detection
0.112016
Vecuum: identification and filtration of false somatic variants caused by recombinant vector contamination · Bioinform. 2016

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

multi-step filtering · 0.3exon junction clipping pattern analysis · 0.2
YearPublicationVenuePosition
2018 AIRVF: a filtering toolbox for precise variant calling in Ion Torrent sequencing
abstract
Summary: Ion Torrent sequencing is one of the most frequently used platforms in healthcare research and industry. Despite many advantages, platform-specific artifacts complicate efficient separation of true variants from errors, especially in variants with lower allele frequencies (<15%). Here, we developed a multi-step filtering toolbox AIRVF that works on flowgram, raw and mapped reads and called variants to reduce artifact-driven false variant calls. Tests on sequencing data of standard reference material showed up to ∼98% reduction of false variants when combined to conventional public pipelines and ∼48% to the in-house commercial solution, with a minimal loss of sensitivity. Availability and implementation: The program with a detailed manual is available at https://sourceforge.net/projects/airvf/. Contact: [email protected]. Supplementary information: Supplementary data are available at Bioinformatics online.
Sunguk Shin 0002, Hyeonju Son, Soonmyung Paik, Sangwoo Kim
Bioinform.3
2016 Vecuum: identification and filtration of false somatic variants caused by recombinant vector contamination
abstract
MOTIVATION: Advances in sequencing technologies have remarkably lowered the detection limit of somatic variants to a low frequency. However, calling mutations at this range is still confounded by many factors including environmental contamination. Vector contamination is a continuously occurring issue and is especially problematic since vector inserts are hardly distinguishable from the sample sequences. Such inserts, which may harbor polymorphisms and engineered functional mutations, can result in calling false variants at corresponding sites. Numerous vector-screening methods have been developed, but none could handle contamination from inserts because they are focusing on vector backbone sequences alone. RESULTS: We developed a novel method-Vecuum-that identifies vector-originated reads and resultant false variants. Since vector inserts are generally constructed from intron-less cDNAs, Vecuum identifies vector-originated reads by inspecting the clipping patterns at exon junctions. False variant calls are further detected based on the biased distribution of mutant alleles to vector-originated reads. Tests on simulated and spike-in experimental data validated that Vecuum could detect 93% of vector contaminants and could remove up to 87% of variant-like false calls with 100% precision. Application to public sequence datasets demonstrated the utility of Vecuum in detecting false variants resulting from various types of external contamination. AVAILABILITY AND IMPLEMENTATION: Java-based implementation of the method is available at http://vecuum.sourceforge.net/ CONTACT: [email protected] information: Supplementary data are available at Bioinformatics online.
Ju Heon Maeng, Jae Seok Lim, Hyeonju Son, June Hawk Lee, Jeong Ho Lee, Sangwoo Kim
Bioinform.4