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Wazim Mohammed Ismail

dblp:184/4729 · DBLP profile ↗
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2ranked-venue papers
1as first author
0since 2021 · last 2016
0000-0002-1782-7296ORCID · corroborated

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

Software engineering, systems software and programming languages · 1 · 1 first-authorApplied, interdisciplinary, general and emerging computing · 1

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 2 heaviest of 3, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
genome annotation
0.212016
MGEScan: a Galaxy-based system for identifying retrotransposons in genomes · Bioinform. 2016
Bioinformatics and computational biology › genome annotation
transposable element annotation
0.212016
MGEScan: a Galaxy-based system for identifying retrotransposons in genomes · Bioinform. 2016

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

python threading · 0.2galaxy workflow · 0.2MPI · 0.2
YearPublicationVenuePosition
2016 Deriving a probability density calculator (functional pearl)
abstract
Given an expression that denotes a probability distribution, often we want a corresponding density function, to use in probabilistic inference. Fortunately, the task of finding a density has been automated. It turns out that we can derive a compositional procedure for finding a density, by equational reasoning about integrals, starting with the mathematical specification of what a density is. Moreover, the density found can be run as an estimation algorithm, as well as simplified as an exact formula to improve the estimate.
Wazim Mohammed Ismail, Chung-chieh Shan
ICFP1
2016 MGEScan: a Galaxy-based system for identifying retrotransposons in genomes
abstract
UNLABELLED: : MGEScan-long terminal repeat (LTR) and MGEScan-non-LTR are successfully used programs for identifying LTRs and non-LTR retrotransposons in eukaryotic genome sequences. However, these programs are not supported by easy-to-use interfaces nor well suited for data visualization in general data formats. Here, we present MGEScan, a user-friendly system that combines these two programs with a Galaxy workflow system accelerated with MPI and Python threading on compute clusters. MGEScan and Galaxy empower researchers to identify transposable elements in a graphical user interface with ready-to-use workflows. MGEScan also visualizes the custom annotation tracks for mobile genetic elements in public genome browsers. A maximum speed-up of 3.26× is attained for execution time using concurrent processing and MPI on four virtual cores. MGEScan provides four operational modes: as a command line tool, as a Galaxy Toolshed, on a Galaxy-based web server, and on a virtual cluster on the Amazon cloud. AVAILABILITY AND IMPLEMENTATION: MGEScan tutorials and source code are available at http://mgescan.readthedocs.org/ CONTACT: [email protected] or [email protected] SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Hyungro Lee, Minsu Lee 0001, Wazim Mohammed Ismail, Mina Rho, Geoffrey C. Fox, Sangyoon Oh 0001, Haixu Tang
Bioinform.3