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	1.	Long-read genome sequencing identifies causal structural variation in a Mendelian disease. [electronic resource] by Merker, Jason D Wenger, Aaron M Sneddon, Tam Grove, Megan Zappala, Zachary Fresard, Laure Waggott, Daryl Utiramerur, Sowmi Hou, Yanli Smith, Kevin S Montgomery, Stephen B Wheeler, Matthew Buchan, Jillian G Lambert, Christine C Eng, Kevin S Hickey, Luke Korlach, Jonas Ford, James Ashley, Euan A Producer: 20181002 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	RNA-Seq mapping and detection of gene fusions with a suffix array algorithm. [electronic resource] by Sakarya, Onur Breu, Heinz Radovich, Milan Chen, Yongzhi Wang, Yulei N Barbacioru, Catalin Utiramerur, Sowmi Whitley, Penn P Brockman, Joel P Vatta, Paolo Zhang, Zheng Popescu, Liviu Muller, Matthew W Kudlingar, Vidya Garg, Nriti Li, Chieh-Yuan Kong, Benjamin S Bodeau, John P Nutter, Robert C Gu, Jian Bramlett, Kelli S Ichikawa, Jeffrey K Hyland, Fiona C Siddiqui, Asim S Producer: 20120801 In: PLoS computational biology vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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