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Control-free calling of copy number alterations in deep-sequencing data using GC-content normalization., , , , , , and . Bioinform., 27 (2): 268-269 (2011)Learning smoothing models of copy number profiles using breakpoint annotations., , , , , , , and . BMC Bioinform., (2013)QuantumClone: clonal assessment of functional mutations in cancer based on a genotype-aware method for clonal reconstruction., , , , , , , , , and 8 other author(s). Bioinform., 34 (11): 1808-1816 (2018)Assessing the Significance of Sets of Words., , , and . CPM, volume 3537 of Lecture Notes in Computer Science, page 358-370. Springer, (2005)SegAnnDB: interactive Web-based genomic segmentation., , , , , , , , , and 2 other author(s). Bioinform., 30 (11): 1539-1546 (2014)Control-FREEC: a tool for assessing copy number and allelic content using next-generation sequencing data., , , , , , , , and . Bioinform., 28 (3): 423-425 (2012)Exact p-value calculation for heterotypic clusters of regulatory motifs and its application in computational annotation of cis-regulatory modules., , , , and . Algorithms Mol. Biol., (2007)Deciphering the etiology and role in oncogenic transformation of the CpG island methylator phenotype: a pan-cancer analysis., and . Briefings Bioinform., (2022)SVDetect: a tool to identify genomic structural variations from paired-end and mate-pair sequencing data., , , , , , , and . Bioinform., 26 (15): 1895-1896 (2010)Nebula - a web-server for advanced ChIP-seq data analysis., , , , and . Bioinform., 28 (19): 2517-2519 (2012)