Systematic Inference of Copy-Number Genotypes from Personal Genome Sequencing Data Reveals Extensive Olfactory Receptor Gene Content Diversity. - Sebastian M. Waszak; Yehudit Hasin; Thomas Zichner; Tsviya Olender; Ifat Keydar; Miriam Khen; Adrian M. Stütz; Andreas Schlattl; Doron Lancet; Jan O. Korbel (PLoS Comput. Biol., 2010)

Identification and removal of low-complexity sites in allele-specific analysis of ChIP-seq data. - Sebastian M. Waszak; Helena Kilpinen; Andreas R. Gschwind; Andrea Orioli; Sunil K. Raghav; Robert M. Witwicki; Eugenia Migliavacca; Alisa Yurovsky; Tuuli Lappalainen; Nouria Hernandez; Alexandre Reymond; Emmanouil T. Dermitzakis; et al. (Bioinform., 2014)

Active medulloblastoma enhancers reveal subgroup-specific cellular origins. - Charles Y. Lin; Serap Erkek; Yiai Tong; Linlin Yin; Alexander J. Federation; Marc Zapatka; Parthiv Haldipur; Daisuke Kawauchi; Thomas Risch; Hans-Jörg Warnatz; Barbara C. Worst; Bensheng Ju; et al. (Nat., 2016)

Genomic basis for RNA alterations in cancer. - Claudia Calabrese; Natalie R. Davidson; Deniz Demircioglu; Nuno A. Fonseca; Yao He; André Kahles; Kjong-Van Lehmann; Fenglin Liu; Yuichi Shiraishi; Cameron M. Soulette; Lara Urban; Liliana Greger; et al. (Nat., 2020)

Analyses of non-coding somatic drivers in 2,658 cancer whole genomes. - Esther Rheinbay; Morten Muhlig Nielsen; Federico Abascal; Jeremiah Wala; Ofer Shapira; Grace Tiao; Henrik Hornshøj; Julian M. Hess; Randi Istrup Juul; Ziao Lin; Lars Feuerbach; Radhakrishnan Sabarinathan; et al. (Nat., 2020)