Additional file 2 of ClinSV: clinical grade structural and copy number variant detection from whole genome sequencing data
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https://springernature.figshare.com/articles/dataset/Additional_file_2_of_ClinSV_clinical_grade_structural_and_copy_number_variant_detection_from_whole_genome_sequencing_data/14121551/1
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资源简介：
Additional file 2. Sample output rare gene affecting variants NA12878. ClinSVClinSV’s output of rare gene affecting variants detected in control sample NA12878.
创建时间：
2021-02-26
