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by Sudmant, Peter H and Rausch, Tobias and Gardner, Eugene J and Handsaker, Robert E and Abyzov, Alexej and Huddleston, John and Zhang, Yan and Ye, Kai and Jun, Goo and Fritz, Markus His-Yang and Konkel, Miriam K and Malhotra, Ankit and Stütz, Adrian M and Shi, Xinghua and Casale, Francesco Paolo and Chen, Jieming and Hormozdiari, Fereydoun and Dayama, Gargi and Chen, Ken and Malig, Maika and Chaisson, Mark J.P and Walter, Klaudia and Meiers, Sascha and Kashin, Seva and Garrison, Erik and Auton, Adam and Lam, Hugo Y.K and Mu, Xinmeng Jasmine and Alkan, Can and Antaki, Danny and Bae, Taejeong and Cerveira, Eliza and Chines, Peter and Chong, Zechen and Clarke, Laura and Dal, Elif and Ding, Li and Emery, Sarah and Fan, Xian and Gujral, Madhusudan and Kahveci, Fatma and Kidd, Jeffrey M and Kong, Yu and Lameijer, Eric-Wubbo and McCarthy, Shane and Flicek, Paul and Gibbs, Richard A and Marth, Gabor and Mason, Christopher E and Menelaou, Androniki and Muzny, Donna M and Nelson, Bradley J and Noor, Amina and Parrish, Nicholas F and Pendleton, Matthew and Quitadamo, Andrew and Raeder, Benjamin and Schadt, Eric E and Romanovitch, Mallory and Schlattl, Andreas and Sebra, Robert and Shabalin, Andrey A and Untergasser, Andreas and Walker, Jerilyn A and Wang, Min and Yu, Fuli and Zhang, Chengsheng and Zhang, Jing and Zheng-Bradley, Xiangqun and Zhou, Wanding and Zichner, Thomas and Sebat, Jonathan and Batzer, Mark A and McCarroll, Steven A and Mills, Ryan E and Gerstein, Mark B and Bashir, Ali and Stegle, Oliver and Devine, Scott E and Lee, Charles and Eichler, Evan E and Korbel, Jan O and Genomes Project Consortium and 1000 Genomes Project Consortium and The 1000 Genomes Project Consortium
Nature, ISSN 0028-0836, 09/2015, Volume 526, Issue 7571, pp. 75 - 81
Journal Article
Nature Genetics, ISSN 1061-4036, 06/2016, Volume 48, Issue 6, pp. 593 - 599
We report the sequences of 1,244 human Y chromosomes randomly ascertained from 26 worldwide populations by the 1000 Genomes Project. We discovered more than... 
GENETIC-VARIATION | AFRICA | EVOLUTION | VARIANTS | EXPANSION | GENETICS & HEREDITY | FRAMEWORK | ANCESTOR | COPY NUMBER VARIATION | INFERENCE | ASSOCIATION | Haplotypes | Chromosomes, Human, Y | Demography | Humans | Male | Polymorphism, Single Nucleotide | Mutation | Phylogeny | Research | Genetic variation | Analysis | Y chromosome | Studies | Genotype & phenotype | Laboratories | Genomes | Grants | Molecular biology | Chromosomes
Journal Article
PLoS computational biology, ISSN 1553-7358, 08/2019, Volume 15, Issue 8, p. e1007293
The Long interspersed nuclear element 1 (LINE-1) is a primary source of genetic variation in humans and other mammals. Despite its importance, LINE-1 activity... 
Transposons | Genetic transcription | Analysis | Genomics | Brain | Medical research | Transcription | Laboratories | Central nervous system | Biochemistry | Genomes | Biology | Genetic diversity | Biophysics | Gene expression | Tissues | Datasets | Medicine | Somatic cells | Cell lines | Stem cells | Neural stem cells | Bioinformatics | Cancer | Tumors
Journal Article
Methods in Molecular Biology, ISSN 1064-3745, 2017, Volume 1541, pp. 167 - 179
Journal Article
by Chaisson, Mark J. P and Sanders, Ashley D and Zhao, Xuefang and Malhotra, Ankit and Porubsky, David and Rausch, Tobias and Gardner, Eugene J and Rodriguez, Oscar L and Guo, Li and Collins, Ryan L and Fan, Xian and Wen, Jia and Handsaker, Robert E and Fairley, Susan and Kronenberg, Zev N and Kong, Xiangmeng and Hormozdiari, Fereydoun and Lee, Dillon and Wenger, Aaron M and Hastie, Alex R and Antaki, Danny and Anantharaman, Thomas and Audano, Peter A and Brand, Harrison and Cantsilieris, Stuart and Cao, Han and Cerveira, Eliza and Chen, Chong and Chen, Xintong and Chin, Chen-Shan and Chong, Zechen and Chuang, Nelson T and Lambert, Christine C and Church, Deanna M and Clarke, Laura and Farrell, Andrew and Flores, Joey and Galeev, Timur and Gorkin, David U and Gujral, Madhusudan and Guryev, Victor and Heaton, William Haynes and Korlach, Jonas and Kumar, Sushant and Kwon, Jee Young and Lam, Ernest T and Lee, Jong Eun and Lee, Joyce and Lee, Wan-Ping and Lee, Sau Peng and Li, Shantao and Marks, Patrick and Viaud-Martinez, Karine and Meiers, Sascha and Munson, Katherine M and Navarro, Fabio C. P and Nelson, Bradley J and Nodzak, Conor and Noor, Amina and Kyriazopoulou-Panagiotopoulou, Sofia and Pang, Andy W. C and Qiu, Yunjiang and Rosanio, Gabriel and Ryan, Mallory and Stütz, Adrian and Spierings, Diana C. J and Ward, Alistair and Welch, AnneMarie E and Xiao, Ming and Xu, Wei and Zhang, Chengsheng and Zhu, Qihui and Zheng-Bradley, Xiangqun and Lowy, Ernesto and Yakneen, Sergei and McCarroll, Steven and Jun, Goo and Ding, Li and Koh, Chong Lek and Ren, Bing and Flicek, Paul and Chen, Ken and Gerstein, Mark B and Kwok, Pui-Yan and Lansdorp, Peter M and Marth, Gabor T and Sebat, Jonathan and Shi, Xinghua and Bashir, Ali and Ye, Kai and Devine, Scott E and Talkowski, Michael E and Mills, Ryan E and Marschall, Tobias and Korbel, Jan O and Eichler, Evan E and Lee, Charles
Nature Communications, ISSN 2041-1723, 12/2019, Volume 10, Issue 1, pp. 1784 - 16
The incomplete identification of structural variants (SVs) from whole-genome sequencing data limits studies of human genetic diversity and disease association.... 
MICRODELETION | GENETIC-VARIATION | RECOMBINATION | ACCURATE | SPERM CELLS | MAPS | MULTIDISCIPLINARY SCIENCES | SEGMENTAL DUPLICATIONS | DIVERSITY | RETROTRANSPOSITION | COPY-NUMBER VARIATION | Metal oxides | Energy transfer | Metals
Journal Article
Journal Article
EUROPEAN JOURNAL OF HUMAN GENETICS, ISSN 1018-4813, 07/2019, Volume 27, Issue 7, pp. 1121 - 1133
Journal Article