Zero Fill Coverage Gaps in Samtools Depth Output

Merging depth output from multiple .bam files can be difficult since Samtools only outputs depth counts for coordinates with non-zero coverage.  If you want to merge depth output from these .bam files you first need to fill in the base pair positions of no coverage with zero values so the depth output for all .bam files is the same length.  Then using a simple UNIX cat you can merge multiple .bam file depth output into one file for comparison and analysis.

Here is a simple Python script to zero fill Samtools depth output:



And below is an example of how to use it:

Generate Coverage Plot in R from Depth Data

Here is a simple way to take coverage data (coverage.depth) and make a plot in R to visualize it.  All you need is a column with base pair coordinates (V1) and a column with respective depth (V2) and you are all set to plug it in the below R code.

Sum Overlapping Base Pairs of Features from Chromosomal BED File

I had a .bed file of genomic features on a chromosome that I wanted to figure out the extent of overlap of the features to investigate commonly covered genes as well as positions where features were likely to form.  I wanted to generate a plot similar to a coverage depth plot from next-generation sequencing reads.  I am sure more efficient methods exist, but here is some Python code that takes in a .bed file of features (features.bed) and creates an output file (features.depth) with the feature overlap "depth" every 5,000 base pairs across the areas which contain features in your chromosomal .bed file.