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收藏High-resolution single-molecule long-fragment rRNA gene amplicon sequencing of bacterial and eukaryotic microbial communities
Fang, Chao; Sun, Xiaohuan; Fan, Fei; Zhang, Xiaowei; Wang, Ou; Zheng, Haotian; Peng, Zhuobing; Luo, Xiaoqing; Chen, Ao; Zhang, Wenwei; Drmanac, Radoje; Peters, Brock A.; Song, Zewei; Kristiansen, Karsten 分享 收藏 A Novel Hierarchical Deep Learning Framework for Diagnosing Multiple Visual Impairment Diseases in the Clinical EnvironmentHong, Jiaxu; Liu, Xiaoqing; Guo, Youwen; Gu, Hao; Gu, Lei; Xu, Jianjiang; Lu, Yi; Sun, Xinghuai; Ye, Zhengqiang; Liu, Jian; Peters, Brock A.; Chen, Jason 分享 收藏 Comparison of long-read methods for sequencing and assembly of a plant genome植物基因组测序和组装的长读方法的比较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. 分享 收藏 TGS-GapCloser: A fast and accurate gap closer for large genomes with low coverage of error-prone long readsTgs-gapcloser: 一种快速准确的大基因组间隙关闭器，具有低的易出错长读数覆盖率Xu, Mengyang; Guo, Lidong; Gu, Shengqiang; Wang, Ou; Zhang, Rui; Peters, Brock A.; Fan, Guangyi; Liu, Xin; Xu, Xun; Deng, Li; Zhang, Yongwei 分享 收藏 Efficient and unique cobarcoding of second-generation sequencing reads from long DNA molecules enabling cost-effective and accurate sequencing, haplotyping, and de novo assemblyWang, Ou; Chin, Robert; Cheng, Xiaofang; Wu, Michelle Ka Yan; Mao, Qing; Tang, Jingbo; Sun, Yuhui; Anderson, Ellis; Lam, Han K.; Chen, Dan; Zhou, Yujun; Wang, Linying; Fan, Fei; Zou, Yan; Xie, Yinlong; Zhang, Rebecca Yu; Drmanac, Snezana; Nguyen, Darlene; Xu, Chongjun; Villarosa, Christian; Gablenz, Scott; Barua, Nina; Nguyen, Staci; Tian, Wenlan; Liu, Jia Sophie; Wang, Jingwan; Liu, Xiao; Qi, Xiaojuan; Chen, Ao; Wang, He; Dong, Yuliang; Zhang, Wenwei; Alexeev, Andrei; Yang, Huanming; Wang, Jian; Kristiansen, Karsten; Xu, Xun; Drmanac, Radoje; Peters, Brock A. 分享 收藏 分享 收藏 3 Branch ligation: a novel method to ligate non-complementary DNA to recessed or internal 3OH ends in DNA or RNAWang, 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 分享 收藏 Clinical and genetic analysis of a rare syndrome associated with neotenyWalker, Richard F.; Ciotlos, Serban; Mao, Qing; Chin, Robert; Drmanac, Snezana; Barua, Nina; Agarwal, Misha R.; Zhang, Rebecca Yu; Li, Zhenyu; Wu, Michelle Ka Yan; Sun, Kevin; Lee, Katharine; Nguyen, Staci; Liu, Jia Sophie; Carnevali, Paolo; Drmanac, Radoje; Peters, Brock A. 分享 收藏 Advanced Whole-Genome Sequencing and Analysis of Fetal Genomes from Amniotic FluidMao, Qing; Chin, Robert; Xie, Weiwei; Deng, Yuqing; Zhang, Wenwei; Xu, Huixin; Zhang, Rebecca Yu; Shi, Quan; Peters, Erin E.; Gulbahce, Natali; Li, Zhenyu; Chen, Fang; Drmanac, Radoje; Peters, Brock A. 分享 收藏 Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patientsMitropoulos, Konstantinos; Papadima, Eleni Merkouri; Xiromerisiou, Georgia; Balasopoulou, Angeliki; Charalampidou, Kyriaki; Galani, Vasiliki; Zafeiri, Krystallia-Vassiliki; Dardiotis, Efthymios; Ralli, Styliani; Deretzi, Georgia; John, Anne; Kydonopoulou, Kyriaki; Papadopoulou, Elpida; di Pardo, Alba; Akcimen, Fulya; Loizedda, Annalisa; Dobricic, Valerija; Novakovic, Ivana; Kostic, Vladimir S.; Mizzi, Clint; Peters, Brock A.; Basak, Nazli; Orru, Sandro; Kiskinis, Evangelos; Cooper, David N.; Gerou, Spyridon; Drmanac, Radoje; Bartsakoulia, Marina; Tsermpini, Evangelia-Eirini; Hadjigeorgiou, Georgios M.; Ali, Bassam R.; Katsila, Theodora; Patrinos, George P. 分享 收藏 Quantitative Whole Genome Sequencing of Circulating Tumor Cells Enables Personalized Combination Therapy of Metastatic CancerGulbahce, Natali; Magbanua, Mark Jesus M.; Chin, Robert; Agarwal, Misha R.; Luo, Xuhao; Liu, Jia; Hayden, Daniel M.; Mao, Qing; Ciotlos, Serban; Li, Zhenyu; Chen, Yanxiang; Chen, Xingpeng; Li, Yuxiang; Yu, Rebecca Zhang; Lee, Katharine; Tearle, Rick; Park, Emily; Drmanac, Snezana; Rugo, Hope S.; Park, John W.; Drmanac, Radoje; Peters, Brock A. 分享 收藏 Novel genetic risk variants for pediatric celiac disease小儿乳糜泻的新型遗传风险变异Balasopoulou, Angeliki; Stankovic, Biljana; Panagiotara, Angeliki; Nikcevic, 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 分享 收藏 The whole genome sequences and experimentally phased haplotypes of over 100 personal genomes超过100个个人基因组的全基因组序列和实验定相单倍型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. 分享 收藏 Premalignant SOX2 overexpression in the fallopian tubes of ovarian cancer patients: Discovery and validation studiesHellner, Karin; Miranda, Fabrizio; Chedom, Donatien Fotso; Herrero-Gonzalez, Sandra; Hayden, Daniel M.; Tearle, Rick; Artibani, Mara; Carrami, Eli M.; Williams, Ruth; Gaitskell, Kezia; Elorbany, Samar; Xu, Ruoyan; Laios, Alex; Buiga, Petronela; Ahmed, Karim; Dhar, Sunanda; Zhang, Rebecca Yu; Campo, Leticia; Myers, Kevin A.; Lozano, Maria; Ruiz-Miro, Maria; Gatius, Sonia; Mota, Alba; Moreno-Bueno, Gema; Matias-Guiu, Xavier; Benitez, Javier; Witty, Lorna; McVean, Gil; Leedham, Simon; Tomlinson, Ian; Drmanac, Radoje; Cazier, Jean-Baptiste; Klein, Robert; Dunne, Kevin; Bast, Robert C., Jr.; Kennedy, Stephen H.; Hassan, Bassim; Lise, Stefano; Jose Garcia, Maria; Peters, Brock A.; Yau, Christopher; Sauka-Spengler, Tatjana; Ahmed, Ahmed Ashour 分享 收藏 分享 收藏 Identification of cancer predisposition variants in apparently healthy individuals using a next-generation sequencing-based family genomics approach使用基于下一代测序的家庭基因组学方法鉴定明显健康个体的癌症易感性变异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. 分享 收藏 分享 收藏 Detection and phasing of single base de novo mutations in biopsies from human in vitro fertilized embryos by advanced whole-genome sequencingPeters, 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; Munne, Santiago; Drmanac, Radoje 分享 收藏 分享 收藏 
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