Fig. 4
From: Combined ultra-low input mRNA and whole-genome sequencing of human embryonic stem cells
Read coverage of genome sequencing and RNA-seq data. a Read coverage of genomic DNA is visualized in a Manhattan plot showing coverage of 10 kb regions over chromosomes. b Example of mapped reads for selected stem cell marker genes (NANOG, POU5F1, SOX2,) and housekeeping gene (ACTB) for both RNA-seq samples (light grey: RNA-seq sample1 and medium grey: RNA-seq sample2) and WGA DNA sample (dark grey). The aligned RNA-seq reads resemble the exon structure depicted below