Shuilin Jin

Orcid: 0000-0002-2318-432X

According to our database1, Shuilin Jin authored at least 17 papers between 2013 and 2022.

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

Timeline

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PhD thesis 
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Links

On csauthors.net:

Bibliography

2022
Correction: SDImpute: A statistical block imputation method based on cell-level and gene-level information for dropouts in single-cell RNA-seq data.
PLoS Comput. Biol., 2022

2021
SDImpute: A statistical block imputation method based on cell-level and gene-level information for dropouts in single-cell RNA-seq data.
PLoS Comput. Biol., 2021

2020
ERDS-Exome: A Hybrid Approach for Copy Number Variant Detection from Whole-Exome Sequencing Data.
IEEE ACM Trans. Comput. Biol. Bioinform., 2020

NDRindex: a method for the quality assessment of single-cell RNA-Seq preprocessing data.
BMC Bioinform., 2020

LAK: Lasso and K-Means Based Single-Cell RNA-Seq Data Clustering Analysis.
IEEE Access, 2020

2019
A Method Based on Differential Entropy-Like Function for Detecting Differentially Expressed Genes Across Multiple Conditions in RNA-Seq Studies.
Entropy, 2019

ProbPFP: a multiple sequence alignment algorithm combining hidden Markov model optimized by particle swarm optimization with partition function.
BMC Bioinform., 2019

BIN1 rs744373 variant shows different association with Alzheimer's disease in Caucasian and Asian populations.
BMC Bioinform., 2019

NDRindex: A method for the quality assessment of single-cell RNA-Seq preprocessing data.
Proceedings of the 2019 IEEE International Conference on Bioinformatics and Biomedicine, 2019

2018
Disease status affects the association between rs4813620 and the expression of Alzheimer's disease susceptibility gene <i>TRIB3</i>.
Proc. Natl. Acad. Sci. USA, 2018

EWAS: epigenome-wide association study software 2.0.
Bioinform., 2018

BIN1 rs744373 Variant Is Significantly Associated with Alzheimer's Disease in Caucasian but Not East Asian Populations.
Proceedings of the Intelligent Computing Theories and Application, 2018

ProbPFP: A Multiple Sequence Alignment Algorithm Combining Partition Function and Hidden Markov Model with Particle Swarm Optimization.
Proceedings of the IEEE International Conference on Bioinformatics and Biomedicine, 2018

2017
DTWscore: differential expression and cell clustering analysis for time-series single-cell RNA-seq data.
BMC Bioinform., 2017

2016
ERDS-pe: A paired hidden Markov model for copy number variant detection from whole-exome sequencing data.
Proceedings of the IEEE International Conference on Bioinformatics and Biomedicine, 2016

2015
LncRNA2Target: a database for differentially expressed genes after lncRNA knockdown or overexpression.
Nucleic Acids Res., 2015

2013
Predicting human microRNA-disease associations based on support vector machine.
Int. J. Data Min. Bioinform., 2013


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