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mTCTScan: a comprehensive platform for annotation and prioritization of mutations affecting drug sensitivity in cancers., , , , , , , , , and 5 other author(s). Nucleic Acids Res., 45 (Webserver-Issue): W215-W221 (2017)GWASdb v2: an update database for human genetic variants identified by genome-wide association studies., , , , , , , , , and 1 other author(s). Nucleic Acids Res., 44 (Database-Issue): 869-876 (2016)Measure transcript integrity using RNA-seq data., , , , , , , , , and 4 other author(s). BMC Bioinform., (2016)Robust and efficient identification of biomarkers by classifying features on graphs., , , , , , , and . Bioinform., 24 (18): 2023-2029 (2008)CpGtools: a python package for DNA methylation analysis., , , , , , , and . Bioinform., 37 (11): 1598-1599 (2021)The Biological Reference Repository (BioR): a rapid and flexible system for genomics annotation., , , , , , , , and . Bioinform., 30 (13): 1920-1922 (2014)A new statistic for identifying batch effects in high-throughput genomic data that uses guided principal component analysis., , , , , , , and . Bioinform., 29 (22): 2877-2883 (2013)Erratum to: Text mining facilitates database curation - extraction of mutation-disease associations from Bio-medical literature., , , , and . BMC Bioinform., (2016)Text mining facilitates database curation - extraction of mutation-disease associations from Bio-medical literature., , , , and . BMC Bioinform., (2015)Detection and visualization of complex structural variants from long reads., , , and . BMC Bioinform., 19-S (20): 67-77 (2018)