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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资源简介：
Additional file 3. Supplementary Tables S1-S9.
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figshare
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2024-09-11
