Search Results - Peters, Brock A.
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TGS-GapCloser: A fast and accurate gap closer for large genomes with low coverage of error-prone long reads by Xu, Mengyang, Guo, Lidong, Gu, Shengqiang, Wang, Ou, Zhang, Rui, Peters, Brock A, Fan, Guangyi, Liu, Xin, Xu, Xun, Deng, Li, Zhang, Yongwei
Published 2020Text -
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Large-scale identification of novel transcripts in the human genome by Peters, Brock A., St. Croix, Brad, Sjöblom, Tobias, Cummins, Jordan M., Silliman, Natalie, Ptak, Janine, Saha, Saurabh, Kinzler, Kenneth W., Hatzis, Christos, Velculescu, Victor E.
Published 2007Text -
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Deep RNA sequencing analysis of readthrough gene fusions in human prostate adenocarcinoma and reference samples by Nacu, Serban, Yuan, Wenlin, Kan, Zhengyan, Bhatt, Deepali, Rivers, Celina Sanchez, Stinson, Jeremy, Peters, Brock A, Modrusan, Zora, Jung, Kenneth, Seshagiri, Somasekar, Wu, Thomas D
Published 2011Text -
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A Novel Hierarchical Deep Learning Framework for Diagnosing Multiple Visual Impairment Diseases in the Clinical Environment by Hong, Jiaxu, Liu, Xiaoqing, Guo, Youwen, Gu, Hao, Gu, Lei, Xu, Jianjiang, Lu, Yi, Sun, Xinghuai, Ye, Zhengqiang, Liu, Jian, Peters, Brock A., Chen, Jason
Published 2021Text -
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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
Published 2013Text -
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Accurate haplotype-resolved assembly reveals the origin of structural variants for human trios by Xu, Mengyang, Guo, Lidong, Du, Xiao, Li, Lei, Peters, Brock A, Deng, Li, Wang, Ou, Chen, Fang, Wang, Jun, Jiang, Zhesheng, Han, Jinglin, Ni, Ming, Yang, Huanming, Xu, Xun, Liu, Xin, Huang, Jie, Fan, Guangyi
Published 2021Text -
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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
Published 2015Text -
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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.
Published 2015Text -
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An ATAC-seq atlas of chromatin accessibility in mouse tissues by Liu, Chuanyu, Wang, Mingyue, Wei, Xiaoyu, Wu, Liang, Xu, Jiangshan, Dai, Xi, Xia, Jun, Cheng, Mengnan, Yuan, Yue, Zhang, Pengfan, Li, Jiguang, Feng, Taiqing, Chen, Ao, Zhang, Wenwei, Chen, Fang, Shang, Zhouchun, Zhang, Xiuqing, Peters, Brock A., Liu, Longqi
Published 2019Text -
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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.
Published 2016Text -
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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
Published 2019Text -
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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
Published 2020Text -
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Somatic mutations in p85α promote tumorigenesis through class IA PI3K activation by Jaiswal, Bijay S., Janakiraman, Vasantharajan, Kljavin, Noelyn M., Chaudhuri, Subhra, Stern, Howard M., Wang, Weiru, Kan, Zhengyan, Dbouk, Hashem A., Peters, Brock A., Waring, Paul, Vega, Trisha Dela, Kenski, Denise M., Bowman, Krista, Lorenzo, Maria, Li, Hong, Wu, Jiansheng, Modrusan, Zora, Stinson, Jeremy, Eby, Michael, Yue, Peng, Kaminker, Josh, de Sauvage, Frederic J., Backer, Jonathan M., Seshagiri, Somasekar
Published 2009Text -
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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
Published 2016Text -
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Accurate whole genome sequencing and haplotyping from10-20 human cells by Peters, Brock A., Kermani, Bahram G., Sparks, Andrew B., Alferov, Oleg, Hong, Peter, Alexeev, Andrei, Jiang, Yuan, Dahl, Fredrik, Tang, Y. Tom, Haas, Juergen, Robasky, Kimberly, Zaranek, Alexander Wait, Lee, Je-Hyuk, Ball, Madeleine Price, Peterson, Joseph E., Perazich, Helena, Yeung, George, Liu, Jia, Chen, Linsu, Kennemer, Michael I., Pothuraju, Kaliprasad, Konvicka, Karel, Tsoupko-Sitnikov, Mike, Pant, Krishna P., Ebert, Jessica C., Nilsen, Geoffrey B., Baccash, Jonathan, Halpern, Aaron L., Church, George M., Drmanac, Radoje
Published 2012Text