Fig.  4From: Allele-specific quantitation of ATXN3 and HTT transcripts in polyQ disease modelsDetermination of endogenous WT and MUT HTT allele expression ratios in HD cell lines. a–c Results from ddPCR are presented as a mean WT and MUT HTT transcript allele abundance, calculated based on results from all three HTT assays (HTT_SNP2, HTT_SNP5 and HTT_SNP7), in iPSCs (a), NSCs (b), and neurons (c). These data were analyzed using unpaired t test. d Corresponding results to a–c presented for HTT_SNP2, HTT_SNP5, and HTT_SNP7 assays separately and analyzed with two-way ANOVA with Tukey’s multiple comparison test for identification of any cell type-specific changes. In this graph, only WT allele abundance is presented, the MUT allele abundance equals a remainder to the sum of 100%). e Estimation of the total number (WT + MUT) of endogenous HTT transcripts per diploid genome using HTT_SNP5 assay. Data were analyzed using unpaired t test. For all experiments presented in this figure n=3. Two-tailed p value < 0.05 was considered significant and is depicted in the figure by: *p < 0.05; **p < 0.01; ***p < 0.001; ****p < 0.0001. All data are presented as means ± SD. Individual data values are available in Additional File 13Back to article page