Additional file 7: of NCBoost classifies pathogenic non-coding variants in Mendelian diseases through supervised learning on purifying selection signals in humans
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Table S6. Feature and pathogenicity scores for intron variant 11:134086816.T > C associated with gene NCAPD3. (XLSX 12 kb)
补充表S6:与NCAPD3基因相关的11号染色体134086816位点T>C内含子变异的特征与致病性评分(XLSX格式,12 kb)
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Yufei Luo创建时间:
2019-02-12



