Evaluating nanopore sequencing data processing pipelines for structural variation identification von Zhou, Anbo, Lin, Timothy, Xing, Jinchuan

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Meiosis interrupted: the genetics of female infertility via meiotic failure von Biswas, Leelabati, Tyc, Katarzyna, El Yakoubi, Warif, Morgan, Katie, Xing, Jinchuan, Schindler, Karen

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Accounting for Protein Subcellular Localization: A Compartmental Map of the Rat Liver Proteome von Jadot, Michel, Boonen, Marielle, Thirion, Jaqueline, Wang, Nan, Xing, Jinchuan, Zhao, Caifeng, Tannous, Abla, Qian, Meiqian, Zheng, Haiyan, Everett, John K., Moore, Dirk F., Sleat, David E., Lobel, Peter

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Genetic Evidence for High-Altitude Adaptation in Tibet von Simonson, Tatum S, Yang, Yingzhong, Huff, Chad D, Yun, Haixia, Qin, Ga, Witherspoon, David J, Bai, Zhenzhong, Lorenzo, Felipe R, Xing, Jinchuan, Jorde, Lynn B, Prchal, Josef T, Ge, RiLi

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Pedigree-based estimation of human mobile element retrotransposition rates von Feusier, Julie, Watkins, W Scott, Thomas, Jainy, Farrell, Andrew, Witherspoon, David J, Baird, Lisa, Ha, Hongseok, Xing, Jinchuan, Jorde, Lynn B

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Genomics and epigenetics guided identification of tissue-specific genomic safe harbors von Shrestha, Dewan, Bag, Aishee, Wu, Ruiqiong, Zhang, Yeting, Tang, Xing, Qi, Qian, Xing, Jinchuan, Cheng, Yong

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Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects von Regier, Allison A., Farjoun, Yossi, Larson, David E., Krasheninina, Olga, Kang, Hyun Min, Howrigan, Daniel P., Chen, Bo-Juen, Kher, Manisha, Banks, Eric, Ames, Darren C., English, Adam C., Li, Heng, Xing, Jinchuan, Zhang, Yeting, Matise, Tara, Abecasis, Goncalo R., Salerno, Will, Zody, Michael C., Neale, Benjamin M., Hall, Ira M.

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Analysis of DNA variants in miRNAs and miRNA 3ʼUTR binding sites in female infertility patients von Tyc, Katarzyna M., Wong, Anthony, Scott, Richard T., Tao, Xin, Schindler, Karen, Xing, Jinchuan

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Worldwide patterns of genomic variation and admixture in gray wolves von Fan, Zhenxin, Silva, Pedro, Gronau, Ilan, Wang, Shuoguo, Armero, Aitor Serres, Schweizer, Rena M, Ramirez, Oscar, Pollinger, John, Galaverni, Marco, Ortega Del-Vecchyo, Diego, Du, Lianming, Zhang, Wenping, Zhang, Zhihe, Xing, Jinchuan, Vilà, Carles, Marques-Bonet, Tomas, Godinho, Raquel, Yue, Bisong, Wayne, Robert K

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Dysregulation of mTOR signaling mediates common neurite and migration defects in both idiopathic and 16p11.2 deletion autism neural precursor cells von Prem, Smrithi, Dev, Bharati, Peng, Cynthia, Mehta, Monal, Alibutud, Rohan, Connacher, Robert J, St Thomas, Madeline, Zhou, Xiaofeng, Matteson, Paul, Xing, Jinchuan, Millonig, James H, DiCicco-Bloom, Emanuel

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SMAD4 Suppresses WNT-Driven Dedifferentiation and Oncogenesis in the Differentiated Gut Epithelium von Perekatt, Ansu O, Shah, Pooja P, Cheung, Shannon, Jariwala, Nidhi, Wu, Alex, Gandhi, Vishal, Kumar, Namit, Feng, Qiang, Patel, Neeket, Chen, Lei, Joshi, Shilpy, Zhou, Anbo, Taketo, M Mark, Xing, Jinchuan, White, Eileen, Gao, Nan, Gatza, Michael L, Verzi, Michael P

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Polymorphic mobile element insertions contribute to gene expression and alternative splicing in human tissues von Cao, Xiaolong, Zhang, Yeting, Payer, Lindsay M, Lords, Hannah, Steranka, Jared P, Burns, Kathleen H, Xing, Jinchuan

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A probabilistic disease-gene finder for personal genomes von Yandell, Mark, Huff, Chad, Hu, Hao, Singleton, Marc, Moore, Barry, Xing, Jinchuan, Jorde, Lynn B, Reese, Martin G

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SMAD4 is critical in suppression of BRAF-V600E serrated tumorigenesis von Tong, Kevin, Kothari, Om A., Haro, Katherine S., Panda, Anshuman, Bandari, Manisha M., Carrick, Jillian N., Hur, Joseph J., Zhang, Lanjing, Chan, Chang S., Xing, Jinchuan, Gatza, Michael L., Ganesan, Shridar, Verzi, Michael P.

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Mutations in ASH1L confer susceptibility to Tourette syndrome von Liu, Shiguo, Tian, Miaomiao, He, Fan, Li, Jiani, Xie, Hong, Liu, Wenmiao, Zhang, Yeting, Zhang, Ru, Yi, Mingji, Che, Fengyuan, Ma, Xu, Zheng, Yi, Deng, Hao, Wang, Guiju, Chen, Lang, Sun, Xue, Xu, Yinglei, Wang, Jingli, Zang, Yucui, Han, Mengmeng, Wang, Xiuhai, Guan, Hongzai, Ge, Yinlin, Wu, Chunmei, Wang, Haiyan, Liang, Hui, Li, Hui, Ran, Ni, Yang, Zhaochuan, Huang, Huanhuan, Wei, Yanzhao, Zheng, Xueping, Sun, Xiangrong, Feng, Xueying, Zheng, Lanlan, Zhu, Tao, Luo, Wenhan, Chen, Qinan, Yan, Yuze, Huang, Zuzhou, Jing, Zhongcui, Guo, Yixia, Zhang, Xuzhan, Schaaf, Christian P., Xing, Jinchuan, Wang, Chuanyue, Yu, Fuli, Guan, Ji-Song

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Whole transcriptome screening for novel genes involved in meiosis and fertility in Drosophila melanogaster von Sun, Siqi, Defosse, Tyler, Boyd, Ayla, Sop, Joel, Verderose, Faith, Surray, Diya, Aziz, Mark, Howland, Margaret, Wu, Siwen, Changela, Neha, Jang, Janet, Schindler, Karen, Xing, Jinchuan, McKim, Kim S.

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Mobile elements create structural variation: analysis of a complete human genome von Xing, Jinchuan, Zhang, Yuhua, Han, Kyudong, Salem, Abdel Halim, Sen, Shurjo K, Huff, Chad D, Zhou, Qiong, Kirkness, Ewen F, Levy, Samuel, Batzer, Mark A, Jorde, Lynn B

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piRNAs derived from ancient viral processed pseudogenes as transgenerational sequence-specific immune memory in mammals von Parrish, Nicholas F, Fujino, Kan, Shiromoto, Yusuke, Iwasaki, Yuka W, Ha, Hongseok, Xing, Jinchuan, Makino, Akiko, Kuramochi-Miyagawa, Satomi, Nakano, Toru, Siomi, Haruhiko, Honda, Tomoyuki, Tomonaga, Keizo

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Whole-exome sequencing identifies genes associated with Tourette’s disorder in multiplex families von Cao, Xiaolong, Zhang, Yeting, Abdulkadir, Mohamed, Deng, Li, Fernandez, Thomas V., Garcia-Delgar, Blanca, Hagstrøm, Julie, Hoekstra, Pieter J., King, Robert A., Koesterich, Justin, Kuperman, Samuel, Morer, Astrid, Nasello, Cara, Plessen, Kerstin J., Thackray, Joshua K., Zhou, Lisheng, Dietrich, Andrea, Tischfield, Jay A., Heiman, Gary A., Xing, Jinchuan

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Ancient hybridization and admixture in macaques (genus Macaca) inferred from whole genome sequences von Fan, Zhenxin, Zhou, Anbo, Osada, Naoki, Yu, Jianqiu, Jiang, Juan, Li, Peng, Du, Lianming, Niu, Lili, Deng, Jiabo, Xu, Huailiang, Xing, Jinchuan, Yue, Bisong, Li, Jing

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