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Tianquan Huang

dblp:370/5508 · DBLP profile ↗
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1ranked-venue papers
0as first author
1since 2021 · last 2023
—ORCID · none

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

Applied, interdisciplinary, general and emerging computing · 1 · 1 since 2021

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 4, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › metagenomics
k-mer-based classification
0.712023
KMCP: accurate metagenomic profiling of both prokaryotic and viral populations by pseudo-mapping · Bioinform. 2023
Bioinformatics and computational biology
metagenomics
0.712023
KMCP: accurate metagenomic profiling of both prokaryotic and viral populations by pseudo-mapping · Bioinform. 2023
Bioinformatics and computational biology › metagenomics
taxonomic profiling
0.712023
KMCP: accurate metagenomic profiling of both prokaryotic and viral populations by pseudo-mapping · Bioinform. 2023

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

pseudo-mapping · 0.7compact bit-sliced signature index · 0.7
YearPublicationVenuePosition
2023 KMCP: accurate metagenomic profiling of both prokaryotic and viral populations by pseudo-mapping
abstract
MOTIVATION: The growing number of microbial reference genomes enables the improvement of metagenomic profiling accuracy but also imposes greater requirements on the indexing efficiency, database size and runtime of taxonomic profilers. Additionally, most profilers focus mainly on bacterial, archaeal and fungal populations, while less attention is paid to viral communities. RESULTS: We present KMCP (K-mer-based Metagenomic Classification and Profiling), a novel k-mer-based metagenomic profiling tool that utilizes genome coverage information by splitting the reference genomes into chunks and stores k-mers in a modified and optimized Compact Bit-Sliced Signature Index for fast alignment-free sequence searching. KMCP combines k-mer similarity and genome coverage information to reduce the false positive rate of k-mer-based taxonomic classification and profiling methods. Benchmarking results based on simulated and real data demonstrate that KMCP, despite a longer running time than all other methods, not only allows the accurate taxonomic profiling of prokaryotic and viral populations but also provides more confident pathogen detection in clinical samples of low depth. AVAILABILITY AND IMPLEMENTATION: The software is open-source under the MIT license and available at https://github.com/shenwei356/kmcp. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Hongyan Xiang, Tianquan Huang, Mingli Peng, Dachuan Cai, Hong Ren
Bioinform.3