Mulin Jun Li
Orcid: 0000-0003-3598-3679
According to our database1,
Mulin Jun Li
authored at least 22 papers
between 2010 and 2024.
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Bibliography
2024
SingleQ: a comprehensive database of single-cell expression quantitative trait loci (sc-eQTLs) cross human tissues.
Database J. Biol. Databases Curation, January, 2024
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
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
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
2015
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
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