Xiao Sun

Orcid: 0000-0003-1048-7775

Affiliations:
  • Southeast University, Nanjing, China


According to our database1, Xiao Sun authored at least 37 papers between 2006 and 2023.

Collaborative distances:
  • Dijkstra number2 of five.
  • Erdős number3 of four.

Timeline

Legend:

Book 
In proceedings 
Article 
PhD thesis 
Dataset
Other 

Links

Online presence:

On csauthors.net:

Bibliography

2023
scAnno: a deconvolution strategy-based automatic cell type annotation tool for single-cell RNA-sequencing data sets.
Briefings Bioinform., May, 2023

Improving the performance of single-cell RNA-seq data mining based on relative expression orderings.
Briefings Bioinform., January, 2023

2022
Relating Translation Efficiency to Protein Networks Provides Evolutionary Insights in Shewanella and Its Implications for Extracellular Electron Transfer.
IEEE ACM Trans. Comput. Biol. Bioinform., 2022

2021
Classification of Mild Cognitive Impairment With Multimodal Data Using Both Labeled and Unlabeled Samples.
IEEE ACM Trans. Comput. Biol. Bioinform., 2021

2019
A Comparative Study of Network Motifs in the Integrated Transcriptional Regulation and Protein Interaction Networks of Shewanella.
IEEE ACM Trans. Comput. Biol. Bioinform., 2019

DNMHMM: An approach to identify the differential nucleosome regions in multiple cell types based on a Hidden Markov Model.
Biosyst., 2019

2018
Nucleosome Positioning of Intronless Genes in the Human Genome.
IEEE ACM Trans. Comput. Biol. Bioinform., 2018

Prediction of microRNA-binding residues in protein using a Laplacian support vector machine based on sequence information.
J. Bioinform. Comput. Biol., 2018

2017
Histone modifications influence skipped exons inclusion.
J. Bioinform. Comput. Biol., 2017

2016
Comparison of the experimental methods in haplotype sequencing via next generation sequencing.
Quant. Biol., 2016

Combinatorial pooled sequencing: experiment design and decoding.
Quant. Biol., 2016

Ehapp2: Estimate haplotype frequencies from pooled sequencing data with prior database information.
J. Bioinform. Comput. Biol., 2016

2015
PRBP: Prediction of RNA-Binding Proteins Using a Random Forest Algorithm Combined with an RNA-Binding Residue Predictor.
IEEE ACM Trans. Comput. Biol. Bioinform., 2015

DectICO: an alignment-free supervised metagenomic classification method based on feature extraction and dynamic selection.
BMC Bioinform., 2015

Accurate estimation of haplotype frequency from pooled sequencing data and cost-effective identification of rare haplotype carriers by overlapping pool sequencing.
Bioinform., 2015

2014
Quantitative group testing-based overlapping pool sequencing to identify rare variant carriers.
BMC Bioinform., 2014

2013
Prioritization of Disease Susceptibility Genes Using LSM/SVD.
IEEE Trans. Biomed. Eng., 2013

Target Identification and Target-centered Network Construction from Biomedical Literature.
J. Softw., 2013

2012
Sequence-Based Prediction of DNA-Binding Residues in Proteins with Conservation and Correlation Information.
IEEE ACM Trans. Comput. Biol. Bioinform., 2012

Nucleosome organization in sequences of alternative events in human genome.
Biosyst., 2012

Next-generation sequencing data processing: Analysis of unmapped reads and extremely high mapped peaks.
Proceedings of the 5th International Conference on BioMedical Engineering and Informatics, 2012

2011
Role of 10-11 bp periodicities of eukaryotic DNA sequence in nucleosome positioning.
Biosyst., 2011

2010
Nucleosomes Are Well Positioned at Both Ends of Exons.
Proceedings of the Life System Modeling and Intelligent Computing, 2010

ATRMiner : A system for automatic biomedical named entities recognition.
Proceedings of the Sixth International Conference on Natural Computation, 2010

2009
Mechanism-anchored profiling derived from epigenetic networks predicts outcome in acute lymphoblastic leukemia.
BMC Bioinform., 2009

Prediction of DNA-binding residues in proteins from amino acid sequences using a random forest model with a hybrid feature.
Bioinform., 2009

SVM-Based Approach for Predicting DNA-Binding Residues in Proteins from Amino Acid Sequences.
Proceedings of the International Joint Conferences on Bioinformatics, 2009

A Hybrid Approach for Biomedical Entity Name Recognition.
Proceedings of the 2nd International Conference on BioMedical Engineering and Informatics, 2009

2008
Coronavirus phylogeny based on Base-Base Correlation.
Int. J. Bioinform. Res. Appl., 2008

Comparability of gene expression in human blood, immune and carcinoma cells.
Appl. Math. Comput., 2008

2007
RF-DYMHC: detecting the yeast meiotic recombination hotspots and coldspots by random forest model using gapped dinucleotide composition features.
Nucleic Acids Res., 2007

MiPred: classification of real and pseudo microRNA precursors using random forest prediction model with combined features.
Nucleic Acids Res., 2007

RFRCDB-siRNA: Improved design of siRNAs by random forest regression model coupled with database searching.
Comput. Methods Programs Biomed., 2007

Meta-analysis of several gene lists for distinct types of cancer: A simple way to reveal common prognostic markers.
BMC Bioinform., 2007

Support Vector Machine for Prediction of DNA-Binding Domains in Protein-DNA Complexes.
Proceedings of the Life System Modeling and Simulation, International Conference, 2007

Informational Structure of Agrobacterium Tumefaciens C58 Genome.
Proceedings of the Life System Modeling and Simulation, International Conference, 2007

2006
Support vector machine for classification of meiotic recombination hotspots and coldspots in Saccharomyces cerevisiaebased on codon composition.
BMC Bioinform., 2006


  Loading...