Search Results - Drmanac, Radoje

Selective DNA amplification from complex genomes using universal double-sided adapters by Callow, Matthew J., Drmanac, Snezana, Drmanac, Radoje

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Co-barcoded sequence reads from long DNA fragments: a cost-effective solution for “perfect genome” sequencing by Peters, Brock A., Liu, Jia, Drmanac, Radoje

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Pure CTCs, advanced WGS, and precise personalized combination therapies by Peters, Brock A., Park, John W., Drmanac, Radoje

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IterCluster: a barcode clustering algorithm for long fragment read analysis by Weng, Jiancong, Chen, Tian, Xie, Yinlong, Xu, Xun, Zhang, Gengyun, Peters, Brock A., Drmanac, Radoje

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Significant abundance of cis configurations of coding variants in diploid human genomes by Hoehe, Margret R, Herwig, Ralf, Mao, Qing, Peters, Brock A, Drmanac, Radoje, Church, George M, Huebsch, Thomas

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Impact of sequencing depth and technology on de novo RNA-Seq assembly by Patterson, Jordan, Carpenter, Eric J., Zhu, Zhenzhen, An, Dan, Liang, Xinming, Geng, Chunyu, Drmanac, Radoje, Wong, Gane Ka-Shu

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Single-cell RNA profiling links ncRNAs to spatiotemporal gene expression during C. elegans embryogenesis by Sun, Yan, Yu, Qichao, Li, Lei, Mei, Zhanlong, Zhou, Biaofeng, Liu, Shang, Pan, Taotao, Wu, Liang, Lei, Ying, Liu, Longqi, Drmanac, Radoje, Ma, Kun, Liu, Shiping

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Truncating mutations of MAGEL2cause Prader-Willi phenotypes and autism by Schaaf, Christian P., Gonzalez-Garay, Manuel L., Xia, Fan, Potocki, Lorraine, Gripp, Karen W., Zhang, Baili, Peters, Brock A., McElwain, Mark A., Drmanac, Radoje, Beaudet, Arthur L., Caskey, C. Thomas, Yang, Yaping

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CoolMPS: evaluation of antibody labeling based massively parallel non-coding RNA sequencing by Li, Yongping, Fehlmann, Tobias, Borcherding, Adam, Drmanac, Snezana, Liu, Sophie, Groeger, Laura, Xu, Chongjun, Callow, Matthew, Villarosa, Christian, Jorjorian, Alexander, Kern, Fabian, Grammes, Nadja, Meese, Eckart, Jiang, Hui, Drmanac, Radoje, Ludwig, Nicole, Keller, Andreas

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Genome dynamics of the human embryonic kidney 293 lineage in response to cell biology manipulations by Lin, Yao-Cheng, Boone, Morgane, Meuris, Leander, Lemmens, Irma, Van Roy, Nadine, Soete, Arne, Reumers, Joke, Moisse, Matthieu, Plaisance, Stéphane, Drmanac, Radoje, Chen, Jason, Speleman, Frank, Lambrechts, Diether, Van de Peer, Yves, Tavernier, Jan, Callewaert, Nico

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Analysis of Genetic Inheritance in a Family Quartet by Whole Genome Sequencing by Roach, Jared C., Glusman, Gustavo, Smit, Arian F.A., Huff, Chad D., Hubley, Robert, Shannon, Paul T., Rowen, Lee, Pant, Krishna P., Goodman, Nathan, Bamshad, Michael, Shendure, Jay, Drmanac, Radoje, Jorde, Lynn B., Hood, Leroy, Galas, David J.

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Detection and phasing of single base de novo mutations in biopsies from human in vitro fertilized embryos by advanced whole-genome sequencing by Peters, Brock A., Kermani, Bahram G., Alferov, Oleg, Agarwal, Misha R., McElwain, Mark A., Gulbahce, Natali, Hayden, Daniel M., Tang, Y. Tom, Zhang, Rebecca Yu, Tearle, Rick, Crain, Birgit, Prates, Renata, Berkeley, Alan, Munné, Santiago, Drmanac, Radoje

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Identification of cancer predisposition variants in apparently healthy individuals using a next-generation sequencing-based family genomics approach by Karageorgos, Ioannis, Mizzi, Clint, Giannopoulou, Efstathia, Pavlidis, Cristiana, Peters, Brock A., Zagoriti, Zoi, Stenson, Peter D., Mitropoulos, Konstantinos, Borg, Joseph, Kalofonos, Haralabos P., Drmanac, Radoje, Stubbs, Andrew, van der Spek, Peter, Cooper, David N., Katsila, Theodora, Patrinos, George P.

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The whole genome sequences and experimentally phased haplotypes of over 100 personal genomes by Mao, Qing, Ciotlos, Serban, Zhang, Rebecca Yu, Ball, Madeleine P., Chin, Robert, Carnevali, Paolo, Barua, Nina, Nguyen, Staci, Agarwal, Misha R., Clegg, Tom, Connelly, Abram, Vandewege, Ward, Zaranek, Alexander Wait, Estep, Preston W., Church, George M., Drmanac, Radoje, Peters, Brock A.

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Assessment of the cPAS-based BGISEQ-500 platform for metagenomic sequencing by Fang, Chao, Zhong, Huanzi, Lin, Yuxiang, Chen, Bing, Han, Mo, Ren, Huahui, Lu, Haorong, Luber, Jacob M, Xia, Min, Li, Wangsheng, Stein, Shayna, Xu, Xun, Zhang, Wenwei, Drmanac, Radoje, Wang, Jian, Yang, Huanming, Hammarström, Lennart, Kostic, Aleksandar D, Kristiansen, Karsten, Li, Junhua

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3′ Branch ligation: a novel method to ligate non-complementary DNA to recessed or internal 3′OH ends in DNA or RNA by Wang, Lin, Xi, Yang, Zhang, Wenwei, Wang, Weimao, Shen, Hanjie, Wang, Xiaojue, Zhao, Xia, Alexeev, Andrei, Peters, Brock A, Albert, Alayna, Xu, Xu, Ren, Han, Wang, Ou, Kirkconnell, Killeen, Perazich, Helena, Clark, Sonya, Hurowitz, Evan, Chen, Ao, Xu, Xun, Drmanac, Radoje, Jiang, Yuan

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Comparison of long-read methods for sequencing and assembly of a plant genome by Murigneux, Valentine, Rai, Subash Kumar, Furtado, Agnelo, Bruxner, Timothy J C, Tian, Wei, Harliwong, Ivon, Wei, Hanmin, Yang, Bicheng, Ye, Qianyu, Anderson, Ellis, Mao, Qing, Drmanac, Radoje, Wang, Ou, Peters, Brock A, Xu, Mengyang, Wu, Pei, Topp, Bruce, Coin, Lachlan J M, Henry, Robert J

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cPAS-based sequencing on the BGISEQ-500 to explore small non-coding RNAs by Fehlmann, Tobias, Reinheimer, Stefanie, Geng, Chunyu, Su, Xiaoshan, Drmanac, Snezana, Alexeev, Andrei, Zhang, Chunyan, Backes, Christina, Ludwig, Nicole, Hart, Martin, An, Dan, Zhu, Zhenzhen, Xu, Chongjun, Chen, Ao, Ni, Ming, Liu, Jian, Li, Yuxiang, Poulter, Matthew, Li, Yongping, Stähler, Cord, Drmanac, Radoje, Xu, Xun, Meese, Eckart, Keller, Andreas

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Reliable multiplex sequencing with rare index mis-assignment on DNB-based NGS platform by Li, Qiaoling, Zhao, Xia, Zhang, Wenwei, Wang, Lin, Wang, Jingjing, Xu, Dongyang, Mei, Zhiying, Liu, Qiang, Du, Shiyi, Li, Zhanqing, Liang, Xinming, Wang, Xiaman, Wei, Hanmin, Liu, Pengjuan, Zou, Jing, Shen, Hanjie, Chen, Ao, Drmanac, Snezana, Liu, Jia Sophie, Li, Li, Jiang, Hui, Zhang, Yongwei, Wang, Jian, Yang, Huanming, Xu, Xun, Drmanac, Radoje, Jiang, Yuan

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Novel genetic risk variants for pediatric celiac disease by Balasopoulou, Angeliki, Stanković, Biljana, Panagiotara, Angeliki, Nikčevic, Gordana, Peters, Brock A., John, Anne, Mendrinou, Effrosyni, Stratopoulos, Apostolos, Legaki, Aigli Ioanna, Stathakopoulou, Vasiliki, Tsolia, Aristoniki, Govaris, Nikolaos, Govari, Sofia, Zagoriti, Zoi, Poulas, Konstantinos, Kanariou, Maria, Constantinidou, Nikki, Krini, Maro, Spanou, Kleopatra, Radlovic, Nedeljko, Ali, Bassam R., Borg, Joseph, Drmanac, Radoje, Chrousos, George, Pavlovic, Sonja, Roma, Eleftheria, Zukic, Branka, Patrinos, George P., Katsila, Theodora

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