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A. K. M. Tauhidul Islam

dblp:152/2545 · DBLP profile ↗
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3ranked-venue papers
2as first author
0since 2021 · last 2018
—ORCID · none

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

Artificial intelligence and machine learning · 2 · 1 first-authorDatabases, data management, data science and information retrieval · 1Applied, 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%
Databases, data mining, and information retrieval
1 paper
Data mining · 100%

Topics — the 2 heaviest of 2, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › sequence analysis
sequence clustering
0.312018
Predicted Edit Distance Based Clustering of Gene Sequences · ICDM 2018
Data mining
clustering
0.312018
Predicted Edit Distance Based Clustering of Gene Sequences · ICDM 2018

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

locality-sensitive hashing · 0.7edit distance prediction · 0.7kmer · 0.3k-mer · 0.3
YearPublicationVenuePosition
2018 Predicted Edit Distance Based Clustering of Gene Sequences
abstract
Effective mining of huge amount of DNA and RNA fragments generated by next generation sequencing (NGS) technologies is facilitated by developing efficient tools to partition these sequence fragments (reads) based on their level of similarities using edit distance. However, edit distance calculation for all pairwise sequence fragments to cluster these huge data sets is a significant performance bottleneck. In this paper we propose a predicted Edit distance based clustering to significantly lower clustering time. Existing clustering methods for sequence fragments, such as, k-mer based VSEARCH and Locality Sensitive Hash based LSH-Div achieve much reduced clustering time but at the cost of significantly lower cluster quality. We show, through extensive performance analysis, clustering based on this predicted Edit distance provides more than 99% accurate clusters while providing an order of magnitude faster clustering time than actual Edit distance based clustering.
Sakti Pramanik, A. K. M. Tauhidul Islam, Shamik Sural
ICDM2
2015 Back translated peptide K-mer search and local alignment in large DNA sequence databases using BoND-SD-tree indexing
abstract
In the past, genome sequence databases had used main memory indexing, such as the suffix tree, for fast sequence searches. With next generation sequencing technologies, the amount of sequence data being generated is huge and main memory indexing is limited by the amount of memory available. K-mer based techniques are being more used for various genome sequence database applications such as local alignment. K-mer can also provide an excellent basis for creating efficient disk based indexing. In this paper, we have proposed a k-mer based database searching and local alignment tool using box queries on BoND-SD-tree indexing. BoND-tree is quite efficient for indexing and searching in Non-Ordered Discrete Data Space (NDDS). We have conducted experiments on searching DNA sequence databases using back translated protein query sequences and have compared with existing methods. We have also implemented local alignment of back translated protein query sequences with large DNA sequence databases using this index based k-mer search. Performances of this local alignment approach has been compared with that of Tblastn of NCBI. The results are quite promising and justify significance of the proposed approach.
A. K. M. Tauhidul Islam, Sakti Pramanik, Xinge Ji, James R. Cole, Qiang Zhu 0001
BIBE1
2015 MapReduce based parallel gene selection method
A. K. M. Tauhidul Islam, Byeong-Soo Jeong, A. T. M. Golam Bari, Chae-Gyun Lim, Seokhee Jeon
Appl. Intell.1