Additional file 3 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_3_of_Identification_of_skewed_X_chromosome_inactivation_using_exome_and_transcriptome_sequencing_in_patients_with_suspected_rare_genetic_disease/26707655/1
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Supplementary Table 2: Samples from the validation and application cohorts that were predicted to be skewed using NGS data with and without the inclusion of escape genes consisting of significantly skewed variant positions.
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
