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SparkINFERNO: a scalable high-throughput pipeline for inferring molecular mechanisms of non-coding genetic variants., , , , , , , , , and 2 other author(s). Bioinform., 36 (12): 3879-3881 (2020)Omnibus and robust deconvolution scheme for bulk RNA sequencing data integrating multiple single-cell reference sets and prior biological knowledge., , , , and . Bioinform., 38 (19): 4530-4536 (2022)SPAR: small RNA-seq portal for analysis of sequencing experiments., , , , , and . Nucleic Acids Res., 46 (Webserver-Issue): W36-W42 (2018)VCPA: genomic variant calling pipeline and data management tool for Alzheimer's Disease Sequencing Project., , , , , , , , , and 1 other author(s). Bioinform., 35 (11): 1985 (2019)Functional annotation of genomic variants in studies of late-onset Alzheimer's disease., , , , , , , , , and 1 other author(s). Bioinform., 34 (16): 2724-2731 (2018)Invited: Multiclass RNA function classification using next-generation sequencing., , , and . ICCABS, page 10. IEEE Computer Society, (2011)VCPA: genomic variant calling pipeline and data management tool for Alzheimer's Disease Sequencing Project., , , , , , , , , and . Bioinform., 35 (10): 1768-1770 (2019)DASHR: database of small human noncoding RNAs., , , , , , , and . Nucleic Acids Res., 44 (Database-Issue): 216-222 (2016)Gene selection for Brain Cancer Classification., , , and . EMBC, page 5846-5849. IEEE, (2006)DASHR 2.0: integrated database of human small non-coding RNA genes and mature products., , , , , and . Bioinform., 35 (6): 1033-1039 (2019)