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

, , , и . Briefings Bioinform., 16 (3): 393-412 (2015)

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Jun Li

Jun Li

Jun Li

Jun Li

Jun Li

 

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CAUSALdb: a database for disease/trait causal variants identified using summary statistics of genome-wide association studies., , , , , , , , , и 8 other автор(ы). Nucleic Acids Res., 48 (Database-Issue): D807-D816 (2020)ChIP-Array: combinatory analysis of ChIP-seq/chip and microarray gene expression data to discover direct/indirect targets of a transcription factor., , , , и . Nucleic Acids Res., 39 (Web-Server-Issue): 430-436 (2011)ChIP-Array 2: integrating multiple omics data to construct gene regulatory networks., , , , , , , и . Nucleic Acids Res., 43 (Webserver-Issue): W264-W269 (2015)Exploring the function of genetic variants in the non-coding genomic regions: approaches for identifying human regulatory variants affecting gene expression., , , и . Briefings Bioinform., 16 (3): 393-412 (2015)GWAS3D: detecting human regulatory variants by integrative analysis of genome-wide associations, chromosome interactions and histone modifications., , , , и . Nucleic Acids Res., 41 (Webserver-Issue): 150-158 (2013)vSampler: fast and annotation-based matched variant sampling tool., , , , , , и . Bioinform., 37 (13): 1915-1917 (2021)GWASdb: a database for human genetic variants identified by genome-wide association studies., , , , , , , , , и . Nucleic Acids Res., 40 (Database-Issue): 1047-1054 (2012)FastPval: a fast and memory efficient program to calculate very low P-values from empirical distribution., , и . Bioinform., 26 (22): 2897-2899 (2010)