检索结果 - Vitsios, Dimitrios

Mantis-ml: Disease-Agnostic Gene Prioritization from High-Throughput Genomic Screens by Stochastic Semi-supervised Learning 由 Vitsios, Dimitrios, Petrovski, Slavé

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Prioritizing non-coding regions based on human genomic constraint and sequence context with deep learning 由 Vitsios, Dimitrios, Dhindsa, Ryan S., Middleton, Lawrence, Gussow, Ayal B., Petrovski, Slavé

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Large-scale analysis of microRNA expression, epi-transcriptomic features and biogenesis 由 Vitsios, Dimitrios M., Davis, Matthew P., van Dongen, Stijn, Enright, Anton J.

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Gene-SCOUT: identifying genes with similar continuous trait fingerprints from phenome-wide association analyses 由 Middleton, Lawrence, Harper, Andrew R, Nag, Abhishek, Wang, Quanli, Reznichenko, Anna, Vitsios, Dimitrios, Petrovski, Slavé

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A MILI-independent piRNA biogenesis pathway empowers partial germline reprogramming 由 Vasilauskaitė, Lina, Vitsios, Dimitrios, Berrens, Rebecca, Carrieri, Claudia, Reik, Wolf, Enright, Anton J, O’Carroll, Dónal

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Mirnovo: genome-free prediction of microRNAs from small RNA sequencing data and single-cells using decision forests 由 Vitsios, Dimitrios M., Kentepozidou, Elissavet, Quintais, Leonor, Benito-Gutiérrez, Elia, van Dongen, Stijn, Davis, Matthew P., Enright, Anton J.

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RNA-sequencing analysis of umbilical cord plasma microRNAs from healthy newborns 由 Brennan, Gary P., Vitsios, Dimitrios M., Casey, Sophie, Looney, Ann-Marie, Hallberg, Boubou, Henshall, David C., Boylan, Geraldine B., Murray, Deirdre M., Mooney, Catherine

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mRNA 3′ uridylation and poly(A) tail length sculpt the mammalian maternal transcriptome 由 Morgan, Marcos, Much, Christian, DiGiacomo, Monica, Azzi, Chiara, Ivanova, Ivayla, Vitsios, Dimitrios M., Pistolic, Jelena, Collier, Paul, Moreira, Pedro, Benes, Vladimir, Enright, Anton J., O’Carroll, Dónal

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A programmed wave of uridylation-primed mRNA degradation is essential for meiotic progression and mammalian spermatogenesis 由 Morgan, Marcos, Kabayama, Yuka, Much, Christian, Ivanova, Ivayla, Di Giacomo, Monica, Auchynnikava, Tatsiana, Monahan, Jack Michael, Vitsios, Dimitrios Michael, Vasiliauskaitė, Lina, Comazzetto, Stefano, Rappsilber, Juri, Allshire, Robin Campbell, Porse, Bo Torben, Enright, Anton James, O’Carroll, Dónal

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Rare variant contribution to human disease in 281,104 UK Biobank exomes 由 Wang, Quanli, Dhindsa, Ryan S., Carss, Keren, Harper, Andrew R., Nag, Abhishek, Tachmazidou, Ioanna, Vitsios, Dimitrios, Deevi, Sri V. V., Mackay, Alex, Muthas, Daniel, Hühn, Michael, Monkley, Susan, Olsson, Henric, Wasilewski, Sebastian, Smith, Katherine R., March, Ruth, Platt, Adam, Haefliger, Carolina, Petrovski, Slavé

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In situ functional dissection of RNA cis-regulatory elements by multiplex CRISPR-Cas9 genome engineering 由 Wu, Qianxin, Ferry, Quentin R. V., Baeumler, Toni A., Michaels, Yale S., Vitsios, Dimitrios M., Habib, Omer, Arnold, Roland, Jiang, Xiaowei, Maio, Stefano, Steinkraus, Bruno R., Tapia, Marta, Piazza, Paolo, Xu, Ni, Holländer, Georg A., Milne, Thomas A., Kim, Jin-Soo, Enright, Anton J., Bassett, Andrew R., Fulga, Tudor A.

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Exome-Based Rare-Variant Analyses in CKD 由 Cameron-Christie, Sophia, Wolock, Charles J., Groopman, Emily, Petrovski, Slavé, Kamalakaran, Sitharthan, Povysil, Gundula, Vitsios, Dimitrios, Zhang, Mengqi, Fleckner, Jan, March, Ruth E., Gelfman, Sahar, Marasa, Maddalena, Li, Yifu, Sanna-Cherchi, Simone, Kiryluk, Krzysztof, Allen, Andrew S., Fellström, Bengt C., Haefliger, Carolina, Platt, Adam, Goldstein, David B., Gharavi, Ali G.

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Identification of a missense variant in SPDL1 associated with idiopathic pulmonary fibrosis 由 Dhindsa, Ryan S., Mattsson, Johan, Nag, Abhishek, Wang, Quanli, Wain, Louise V., Allen, Richard, Wigmore, Eleanor M., Ibanez, Kristina, Vitsios, Dimitrios, Deevi, Sri V. V., Wasilewski, Sebastian, Karlsson, Maria, Lassi, Glenda, Olsson, Henric, Muthas, Daniel, Monkley, Susan, Mackay, Alex, Murray, Lynne, Young, Simon, Haefliger, Carolina, Maher, Toby M., Belvisi, Maria G., Jenkins, Gisli, Molyneaux, Philip L., Platt, Adam, Petrovski, Slavé

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Spontaneous Coronary Artery Dissection: Insights on Rare Genetic Variation From Genome Sequencing 由 Carss, Keren J., Baranowska, Anna A., Armisen, Javier, Webb, Tom R., Hamby, Stephen E., Premawardhana, Diluka, Al-Hussaini, Abtehale, Wood, Alice, Wang, Quanli, Deevi, Sri V. V., Vitsios, Dimitrios, Lewis, Samuel H., Kotecha, Deevia, Bouatia-Naji, Nabila, Hesselson, Stephanie, Iismaa, Siiri E., Tarr, Ingrid, McGrath-Cadell, Lucy, Muller, David W., Dunwoodie, Sally L., Fatkin, Diane, Graham, Robert M., Giannoulatou, Eleni, Samani, Nilesh J., Petrovski, Slavé, Haefliger, Carolina, Adlam, David

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Re-annotation of 191 developmental and epileptic encephalopathy-associated genes unmasks de novo variants in SCN1A 由 Steward, Charles A., Roovers, Jolien, Suner, Marie-Marthe, Gonzalez, Jose M., Uszczynska-Ratajczak, Barbara, Pervouchine, Dmitri, Fitzgerald, Stephen, Viola, Margarida, Stamberger, Hannah, Hamdan, Fadi F., Ceulemans, Berten, Leroy, Patricia, Nava, Caroline, Lepine, Anne, Tapanari, Electra, Keiller, Don, Abbs, Stephen, Sanchis-Juan, Alba, Grozeva, Detelina, Rogers, Anthony S., Diekhans, Mark, Guigó, Roderic, Petryszak, Robert, Minassian, Berge A., Cavalleri, Gianpiero, Vitsios, Dimitrios, Petrovski, Slavé, Harrow, Jennifer, Flicek, Paul, Lucy Raymond, F., Lench, Nicholas J., Jonghe, Peter De, Mudge, Jonathan M., Weckhuysen, Sarah, Sisodiya, Sanjay M., Frankish, Adam

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