Mulin Jun Li

According to our database1, Mulin Jun Li authored at least 21 papers between 2010 and 2023.

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

Timeline

Legend:

Book 
In proceedings 
Article 
PhD thesis 
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Links

On csauthors.net:

Bibliography

2023
Inferring CTCF-binding patterns and anchored loops across human tissues and cell types.
Patterns, August, 2023

QTLbase2: an enhanced catalog of human quantitative trait loci on extensive molecular phenotypes.
Nucleic Acids Res., January, 2023

2022
VannoPortal: multiscale functional annotation of human genetic variants for interrogating molecular mechanism of traits and diseases.
Nucleic Acids Res., 2022

webTWAS: a resource for disease candidate susceptibility genes identified by transcriptome-wide association study.
Nucleic Acids Res., 2022

2021
vSampler: fast and annotation-based matched variant sampling tool.
Bioinform., 2021

2020
QTLbase: an integrative resource for quantitative trait loci across multiple human molecular phenotypes.
Nucleic Acids Res., 2020

CAUSALdb: a database for disease/trait causal variants identified using summary statistics of genome-wide association studies.
Nucleic Acids Res., 2020

Methods and resources to access mutation-dependent effects on cancer drug treatment.
Briefings Bioinform., 2020

2018
GWAS4D: multidimensional analysis of context-specific regulatory variant for human complex diseases and traits.
Nucleic Acids Res., 2018

A powerful approach reveals numerous expression quantitative trait haplotypes in multiple tissues.
Bioinform., 2018

2017
mTCTScan: a comprehensive platform for annotation and prioritization of mutations affecting drug sensitivity in cancers.
Nucleic Acids Res., 2017

2016
GWASdb v2: an update database for human genetic variants identified by genome-wide association studies.
Nucleic Acids Res., 2016

Predicting regulatory variants with composite statistic.
Bioinform., 2016

2015
ChIP-Array 2: integrating multiple omics data to construct gene regulatory networks.
Nucleic Acids Res., 2015

Exploring the function of genetic variants in the non-coding genomic regions: approaches for identifying human regulatory variants affecting gene expression.
Briefings Bioinform., 2015

2014
dbPSHP: a database of recent positive selection across human populations.
Nucleic Acids Res., 2014

DDGni: Dynamic delay gene-network inference from high-temporal data using gapped local alignment.
Bioinform., 2014

2013
GWAS3D: detecting human regulatory variants by integrative analysis of genome-wide associations, chromosome interactions and histone modifications.
Nucleic Acids Res., 2013

2012
GWASdb: a database for human genetic variants identified by genome-wide association studies.
Nucleic Acids Res., 2012

2011
ChIP-Array: combinatory analysis of ChIP-seq/chip and microarray gene expression data to discover direct/indirect targets of a transcription factor.
Nucleic Acids Res., 2011

2010
FastPval: a fast and memory efficient program to calculate very low <i>P</i>-values from empirical distribution.
Bioinform., 2010


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