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All papers authored by Julio Fernandez Banet

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2016 Shiyong Li, Yoon-La Choi, Zhuolin Gong, Xiao Liu, Maruja Lira, Zhengyan Kan, Ensel Oh, Jian Wang, Jason C. Ting, Xiangsheng Ye, Christoph Reinhart, Xiaoqiao Liu, Yunfei Pei, Wei Zhou, Ronghua Chen and 10 other authors

Comprehensive Characterization of Oncogenic Drivers in Asian Lung Adenocarcinoma

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Bronwen L. Aken, Sarah Ayling, Daniel Barrell, Laura Clarke

ORCID

, Valery Curwen, Susan Fairley

ORCID

, Julio Fernandez Banet

ORCID

, Konstantinos Billis, Carlos García Girón, Thibaut Hourlier, Kevin Howe, Andreas Kähäri, Felix Kokocinski, Fergal J. Martin, Daniel N. Murphy and 9 other authors

The Ensembl gene annotation system

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2015 Julio Fernandez-Banet

ORCID

, Anthony Esposito, Scott Coffin, Istvan Boerner Horvath, Heather Estrella, Sabine Schefzick, Shibing Deng, Kai Wang, Keith AChing, Ying Ding, Peter Roberts, Paul A. Rejto, Zhengyan Kan

ORCID

OASIS: web-based platform for exploring cancer multi-omics data

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Julio Fernandez-Banet

ORCID

, Anthony Esposito, Scott Coffin, Sabine Schefzick, Ying Ding, Keith Ching, Istvan Horvath, Peter Roberts, Paul Rejto, Zhengyan Kan

Abstract 4874: OASIS: A centralized portal for cancer omics data analysis

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Damian Smedley, Syed Haider, Steffen Durinck, Luca Pandini, Philippe Bardou, Paolo Provero, Tim Beck, Andrew Blake, Merideth Bonierbale, James Allen, Anthony J. Brookes, Gabriele Bucci, Olivier Arnaiz, Iwan Buetti, Sarah Burge and 92 other authors

The BioMart community portal: an innovative alternative to large, centralized data repositories

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Keith A. Ching, Kai Wang, Zhengyan Kan, Wenyan Zhong, Jarek Kostrowicki, Tao Xie, Zhou Zhu, Jean-Francois Martini, Maria Koehler, Paul Rejto, Julio Fernandez

ORCID

, Kim Arndt

Cell Index Database (CELLX): a web tool for cancer precision medicine

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2014 Tao Xie, Yong Beom Cho, Kai Wang, Donghui Huang, Hye Kyung Hong, Yoon-La Choi, Young Hyeh Ko, Do-Hyun Nam, Juyoun Jin, Heekyoung Yang, Julio Fernandez

ORCID

, Shibing Deng, Paul A. Rejto, Woo Yong Lee, Mao Mao

Patterns of somatic alterations between matched primary and metastatic colorectal tumors characterized by whole-genome sequencing

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Kai Wang, St Yuen, Jiangchun Xu, Sp Lee, Hhn Yan, St Shi, Hc Siu, Shibing Deng, Km Chu, Syk Law, Kh Chan, Asy Chan, Wy Tsui, Rsl Ho, Siu Lun Ho and 16 other authors

Whole-genome sequencing and comprehensive molecular profiling identify new driver mutations in gastric cancer

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2013 Zhengyan Kan, Hancheng Zheng, Xiao Liu, Shuyu Li, Thomas D. Barber, Zhuolin Gong, Huan Gao, Ke Hao, Melinda D. Willard, Jiangchun Xu, Robert Hauptschein, Paul A. Rejto, Julio Fernandez

ORCID

, Guan Wang, Qinghui Zhang and 35 other authors

Whole-genome sequencing identifies recurrent mutations in hepatocellular carcinoma

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2011 Mikhail Gostev, Adam Faulconbridge, Marco Brandizi, Julio Fernandez-Banet

ORCID

, Ugis Sarkans, Alvis Brazma, Helen Parkinson

The BioSample Database (BioSD) at the European Bioinformatics Institute

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Jonathan M. Mudge, Adam Frankish

ORCID

, Julio Fernandez-Banet

ORCID

ORCID

, Thomas Derrien, Cédric Howald, Alexandre Reymond, Roderic Guigó, Tim Hubbard, Jennifer Harrow

The Origins, Evolution, and Functional Potential of Alternative Splicing in Vertebrates

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2010 Mikhail Gostev, Julio Fernandez Banet

ORCID

, Johan Rung, Joern Dietrich, Inga Prokopenko

ORCID

, Samuli Ripatti, Mi I. McCarthy, Alvis Brazma, Maria Krestyaninova

SAIL-a software system for sample and phenotype availability across biobanks and cohorts

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2009 Paul Flicek, Bronwen L. Aken, Benoit Ballester, Kathryn Beal, Eugene Bragin, Simon Brent, Yuan Chen, Peter Clapham, Guy Coates, Susan Fairley

ORCID

, Stephen Fitzgerald, Julio Fernandez-Banet

ORCID

, Leo Gordon, Stefan Graf, Syed Haider and 44 other authors

Ensembl's 10th year

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Kim D. Pruitt, Jennifer Harrow, Rachel A. Harte, Craig Wallin, Mark Diekhans, Donna R. Maglott, Steve Searle, Catherine M. Farrell, Jane E. Loveland

ORCID

, Barbara J. Ruef, Elizabeth Hart, Marie-Marthe Suner, Bronwen Aken, Melissa J. Landrum, Sarah Ayling and 34 other authors

The consensus coding sequence (CCDS) project: Identifying a common protein-coding gene set for the human and mouse genomes

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2005 Xosé M. Lens, Julio F. Banet

ORCID

, Patricia Outeda, Vicente Barrio-Lucía

A Novel Pattern of Mutation in Uromodulin Disorders: Autosomal Dominant Medullary Cystic Kidney Disease Type 2, Familial Juvenile Hyperuricemic Nephropathy, and Autosomal Dominant Glomerulocystic Kidney Disease

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2004 Wânia Rezende-Lima, Kleber S. Parreira, Miguel García-González, Eva V. A. Riveira, Julio F. Banet

ORCID

, Xosé M. Lens

Homozygosity for uromodulin disorders: FJHN and MCKD-type 2

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