Additional file 10 of Reference genome and transcriptome informed by the sex chromosome complement of the sample increase ability to detect sex differences in gene expression from RNA-Seq data

  • Jocelyn P. Andrews (Contributor)
  • Kimberly C. Olney (Contributor)
  • Valeria A. Valverde-Vesling (Contributor)
  • Melissa Wilson (Contributor)
  • Sarah M. Brotman (Contributor)

Dataset

Description

Additional file 10: X chromosome expression differences between default and sex chromosome complement informed alignment. X chromosome gene expression differences between default and sex chromosome complement informed alignment. Increase in expression when aligned to a sex chromosome complement informed reference genome is a log2 fold change (FC) > 0. A decrease in expression when aligned to a sex chromosome complement informed reference genome is log2 FC < 0. Female XX samples are indicated by red and pink circles for PAR1, XTR, PAR2 genes, and for all other X chromosome genes respectively. Blue and light blue squares represent male XY samples. Blue squares indicate which gene points are in PAR1, XTR, and PAR2, and light blue squares are for genes outside of those regions. Differences in X chromosome expression between reference genomes default and sex chromosome complement for male XY and female XX samples aligned using HISAT for the whole X chromosome and the first 5 Mb are shown for the whole blood (A and B, respectively), brain cortex (E and F, respectively), breast (I and J, respectively), liver (M and N, respectively), and thyroid (Q and R, respectively). Differences in X chromosome expression between reference genomes for male XY and female XX samples aligned using STAR for the whole X chromosome and the first 5 Mb are shown for the whole blood (C and D, respectively), brain cortex (G and H, respectively), breast (K and L, respectively), liver (O and P, respectively), and thyroid (S and T, respectively).
Date made availableJul 21 2020
Publisherfigshare Academic Research System

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