Additional file 2 of Identification of skewed X chromosome inactivation using exome and transcriptome sequencing in patients with suspected rare genetic disease
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https://springernature.figshare.com/articles/dataset/Additional_file_2_of_Identification_of_skewed_X_chromosome_inactivation_using_exome_and_transcriptome_sequencing_in_patients_with_suspected_rare_genetic_disease/25622088/1
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Supplementary Table 1: List of samples from the validation and application cohorts with age, percentage of significantly skewed variants, predicted X-skew status, number of variants evaluated using the position, gene and global models and list of genes in patients predicted to be skewed.
提供机构：
Pinto e Vairo, Filippo; Macke, Erica L; Schultz-Rogers, Laura E; Mulvihill, Lindsay A; Fadra, Numrah; Chanana, Pritha; Oliver, Gavin R; Olson, Rory J; Klee, Eric W; Jenkinson, Garrett; Ferrer, Alejandro; Cousin, Margot A
创建时间：
2024-08-15
