Whole exome sequencing analysis pipeline for the discovery of mutations causative of human rare diseases - researchr publication authors

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Francisco Javier Lopez Domingo, Antonio Rueda Martin, Javier P. Florido, Alicia Vela Boza, Pablo Arce Garcia, Luis Miguel Cruz Renedo, Javier Escalante, Ana Isabel Lopez Perez, Federica Trombetta, Guillermo Antinolo, Javier Santoyo Lopez. Whole exome sequencing analysis pipeline for the discovery of mutations causative of human rare diseases. In Ignacio Rojas, Francisco M. Ortuño Guzman, editors, International Work-Conference on Bioinformatics and Biomedical Engineering, IWBBIO 2013, Granada, Spain, March 18-20, 2013. Proceedings. pages 253-254, Copicentro Editorial, 2013. [doi]

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