Additional file 3 of Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseases
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https://springernature.figshare.com/articles/dataset/Additional_file_3_of_Structural_and_non-coding_variants_increase_the_diagnostic_yield_of_clinical_whole_genome_sequencing_for_rare_diseases/26990317/1
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Additional file 3. Supplementary Tables S1-S9.
提供机构：
Baños-Piñero, Benito; Thakker, Rajesh V.; Camps, Carme; Schilling, Kyleen D.; Hughes, Jim R.; Schwessinger, Ron; Popitsch, Niko; Kane, Maureen; Javaid, Kassim; Cilliers, Deirdre; van Wijk, Richard; Blair, Edward; Davies, E. Graham; Sen, Arjune; Twigg, Stephen R. F.; Roy, Noémi; Hartley, Jane; Dhalla, Fatima; Guerrini, Renzo; Mason, Joanne; Pugh, Chris; Schuh, Anna H.; Dong, Yin; Kesim, Yesim; Vavoulis, Dimitrios V.; Roberts, Irene; Ben-Ami, Tal; Banka, Siddharth; Kelly, Dominic; Pentony, Melissa M.; Marsden, Brian; Wilkie, Andrew O. M.; Mansour, Sahar; Lines, Kate E.; Calpena, Eduardo; Okoli, Steven; Bull, Katherine R.; Maroofian, Reza; Lunter, Gerton; Manzur, Adnan; Watkins, Hugh; Sanders, Edward; Wall, Steven; Lester, Tracy; Brasch-Andersen, Charlotte; Ramesh, Archana; Harris, Adrian L.; Wang, Jing; Stevenson, Mark; Patel, Smita Y.; Lord, Simon R.; Knight, Samantha J. L.; Kvikstad, Erika M.; Rad, Aboulfazl; Bento, Celeste; Langman, Craig B.; Hashimoto, Akiko; Németh, Andrea H.; V
创建时间：
2024-09-11
