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Xinying Jia

dblp:150/1323 · DBLP profile ↗
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2ranked-venue papers
0as first author
1since 2021 · last 2023
0000-0003-0133-8321ORCID · corroborated

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

Applied, interdisciplinary, general and emerging computing · 2 · 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%
Software engineering, system software, and programming languages
1 paper
Programming languages and type systems · 100%

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

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
sequence analysis
0.212014
Bioclojure: a functional library for the manipulation of biological sequences · Bioinform. 2014
Programming languages and type systems
functional programming
0.112014
Bioclojure: a functional library for the manipulation of biological sequences · Bioinform. 2014
Programming languages and type systems
lazy evaluation
0.112014
Bioclojure: a functional library for the manipulation of biological sequences · Bioinform. 2014

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

lazy evaluation · 0.4functional programming · 0.4concurrency · 0.4
YearPublicationVenuePosition
2023 Designing antimicrobial peptides using deep learning and molecular dynamic simulations
abstract
With the emergence of multidrug-resistant bacteria, antimicrobial peptides (AMPs) offer promising options for replacing traditional antibiotics to treat bacterial infections, but discovering and designing AMPs using traditional methods is a time-consuming and costly process. Deep learning has been applied to the de novo design of AMPs and address AMP classification with high efficiency. In this study, several natural language processing models were combined to design and identify AMPs, i.e. sequence generative adversarial nets, bidirectional encoder representations from transformers and multilayer perceptron. Then, six candidate AMPs were screened by AlphaFold2 structure prediction and molecular dynamic simulations. These peptides show low homology with known AMPs and belong to a novel class of AMPs. After initial bioactivity testing, one of the peptides, A-222, showed inhibition against gram-positive and gram-negative bacteria. The structural analysis of this novel peptide A-222 obtained by nuclear magnetic resonance confirmed the presence of an alpha-helix, which was consistent with the results predicted by AlphaFold2. We then performed a structure-activity relationship study to design a new series of peptide analogs and found that the activities of these analogs could be increased by 4-8-fold against Stenotrophomonas maltophilia WH 006 and Pseudomonas aeruginosa PAO1. Overall, deep learning shows great potential in accelerating the discovery of novel AMPs and holds promise as an important tool for developing novel AMPs.
Qiushi Cao, Cheng Ge, Peta J. Harvey, Xianghong Wang, Xinying Jia, Mehdi Mobli, David J. Craik, Tao Jiang 0057, Jinbo Yang, Zhiqiang Wei 0002, Yan Wang 0114, Shan Chang, Rilei Yu
Briefings Bioinform.8
2014 Bioclojure: a functional library for the manipulation of biological sequences
abstract
MOTIVATION: BioClojure is an open-source library for the manipulation of biological sequence data written in the language Clojure. BioClojure aims to provide a functional framework for the processing of biological sequence data that provides simple mechanisms for concurrency and lazy evaluation of large datasets. RESULTS: BioClojure provides parsers and accessors for a range of biological sequence formats, including UniProtXML, Genbank XML, FASTA and FASTQ. In addition, it provides wrappers for key analysis programs, including BLAST, SignalP, TMHMM and InterProScan, and parsers for analyzing their output. All interfaces leverage Clojure's functional style and emphasize laziness and composability, so that BioClojure, and user-defined, functions can be chained into simple pipelines that are thread-safe and seamlessly integrate lazy evaluation. AVAILABILITY AND IMPLEMENTATION: BioClojure is distributed under the Lesser GPL, and the source code is freely available from GitHub (https://github.com/s312569/clj-biosequence).
Jordan Plieskatt, Gabriel Rinaldi, Paul J. Brindley, Xinying Jia, Jeremy Potriquet, Jeffrey Bethony, Jason P. Mulvenna
Bioinform.4