Figure 1
From: Light-RCV: a lightweight read coverage viewer for next generation sequencing data
Appearance of Light-RCV. The user interface of Light-RCV: (a) Sample: switching among different compiled NGS data / (b) Range by: an option for specify a genomic range by coordinate range or by a gene name / (c) Coordinate: chromosome number/name, start position and end position / (d) Gene: a search box for gene name / (e) View: button to show the read coverage in the specified range / (f) Export: saving the current view to an image file / (g) Setting: used to show/hide the compilation panel / (h) Detailed information of the point hovered by the mouse / (i) Main plot of the read coverages / (j) Legend of the plot for showing/hiding the tracks / (k) Annotation track, would show if gtf file is provided at the compilation stage / (l) Bar chart for the mismatch rate / (m) Navigator bar for zooming and scrolling the viewing range / (n) Compilation panel for compiling NGS data.