Demonstration venue · read-only. Every page can be browsed; the buttons that would change it are switched off. Create an account to run TaxoReview on your own data. A simulation from public publication records: the people listed were not invited and did not agree to review.
? Tutorial for this page

Yelei Tang

dblp:313/5171 · DBLP profile ↗
← Back
1ranked-venue papers
0as first author
1since 2021 · last 2022
—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 3, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › sequence analysis
genomic sequence analysis
0.612022
KCOSS: an ultra-fast k-mer counter for assembled genome analysis · Bioinform. 2022
Bioinformatics and computational biology › sequence analysis › k-mer analysis
k-mer counting
0.612022
KCOSS: an ultra-fast k-mer counter for assembled genome analysis · Bioinform. 2022
Bioinformatics and computational biology › sequence analysis › sequence assembly
whole genome assembly analysis
0.612022
KCOSS: an ultra-fast k-mer counter for assembled genome analysis · Bioinform. 2022

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

lock-free thread pool · 0.6lock-free queue · 0.6cuckoo hash table · 0.6bloom filter · 0.6
YearPublicationVenuePosition
2022 KCOSS: an ultra-fast k-mer counter for assembled genome analysis
abstract
MOTIVATION: The k-mer frequency in whole genome sequences provides researchers with an insightful perspective on genomic complexity, comparative genomics, metagenomics and phylogeny. The current k-mer counting tools are typically slow, and they require large memory and hard disk for assembled genome analysis. RESULTS: We propose a novel and ultra-fast k-mer counting algorithm, KCOSS, to fulfill k-mer counting mainly for assembled genomes with segmented Bloom filter, lock-free queue, lock-free thread pool and cuckoo hash table. We optimize running time and memory consumption by recycling memory blocks, merging multiple consecutive first-occurrence k-mers into C-read, and writing a set of C-reads to disk asynchronously. KCOSS was comparatively tested with Jellyfish2, CHTKC and KMC3 on seven assembled genomes and three sequencing datasets in running time, memory consumption, and hard disk occupation. The experimental results show that KCOSS counts k-mer with less memory and disk while having a shorter running time on assembled genomes. KCOSS can be used to calculate the k-mer frequency not only for assembled genomes but also for sequencing data. AVAILABILITYAND IMPLEMENTATION: The KCOSS software is implemented in C++. It is freely available on GitHub: https://github.com/kcoss-2021/KCOSS. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Deyou Tang, Daqiang Tan, Juan Fu, Yelei Tang, Jiabin Lin, Hongli Du, Zhongming Zhao
Bioinform.5