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Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotransposition, , , , , , , , , and 115 other author(s). Nature Genetics, (2020)Random Forest as a Tumour Genetic Marker Extractor., , , , , , and . CoRR, (2019)Analyses of non-coding somatic drivers in 2,658 cancer whole genomes., , , , , , , , , and 179 other author(s). Nat., 578 (7793): 102-111 (2020)BLAST2GENE: a comprehensive conversion of BLAST output into independent genes and gene fragments., , and . Bioinform., 20 (12): 1968-1970 (2004)BLUEPRINT to decode the epigenetic signature written in blood, , , , , , , , , and 47 other author(s). Nature biotechnology, 30 (3): 224–226 (2012)Identification and Analysis of Genes and Pseudogenes within Duplicated Regions in the Human and Mouse Genomes., , , and . PLoS Comput. Biol., (2006)ReLA, a local alignment search tool for the identification of distal and proximal gene regulatory regions and their conserved transcription factor binding sites., , , , , , and . Bioinform., 28 (6): 763-770 (2012)Comprehensive characterization of complex structural variations in cancer by directly comparing genome sequence reads, , , , , , , , , and 10 other author(s). Nature Biotechnology, 32 (11): 1106--1112 (Oct 26, 2014)PAL2NAL: robust conversion of protein sequence alignments into the corresponding codon alignments., , and . Nucleic Acids Res., 34 (Web-Server-Issue): 609-612 (2006)DNAlive: a tool for the physical analysis of DNA at the genomic scale., , , , and . Bioinform., 24 (15): 1731-1732 (2008)