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. 2022 May 6;12:869108. doi: 10.3389/fonc.2022.869108

Figure 1.

Figure 1

Characteristics of the sequencing runs. Samples were run in four batches under different conditions. (A) Number of sequencing reads mapping to features of interest (exons) per sequencing batch, non-corrected (left), after mitochondrial transcript removal (right). (B) Intron to exon ratio per sequencing batch. (C) Principal component analysis after normalization and variance-stabilizing transformation of samples before (left) and after batch correction (right). (D) Distance matrices between samples before (left) and after (right) batch correction. Each row and column represent a single sample, and the diagonal represents samples that are identical. A higher distance score represents higher dissimilarity between a pair of samples. Sample annotation is shown by multiple variables, such as: batch, whether a patient has cancer or not, whether they received 100mg or 200mg of APG-157 or Placebo, treatment time point and patient ID. We have included the same batch and cross-batch technical replicates for a portion of the samples. (E) The distribution of exon occupancy across all genes with 2 or more exons; a value of 1 means full occupancy; a value between 0 and 1 means partial exon occupancy; genes with no exon occupancy have been removed from the dataset. (F) An IGV screenshot showing the coverage of ACTB as a representative gene with full exon occupancy.