SAMtools is a suite of commands for dealing with databases of mapped reads. You'll be using it quite a bit throughout the course.
Calling variants in reads mapped by bowtie
Right now, we'll be using it to call variants (find mutations) in the re-sequenced E. coli genome from the Mapping tutorial. You will need the output SAM files from that tutorial to continue here. We assume that you are still in the main directory of
intro_to_mapping data that you copied to
Load the SAMtools module (if not already loaded):
What version of samtools is loaded on TACC?
Create a new output directory:
Let's copy over the read alignment file in the SAM format and the reference genome in FASTA format to the new directory, so that we don't have so many files cluttering our space.
Index the reference file. (This isn't indexing it for mapping. It's indexing it so that SAMtools can quickly jump to a certain base in the reference.)
Take a look at the new *.fai file that was created by this command. Any idea what some of the numbers mean?
SAM is a text file, so it is slow to access information about how any given read was mapped. SAMtools and many of the commands that we will run later work on BAM files (essentially GZIP compressed binary forms of the text SAM files). These can be loaded much more quickly. Typically, they also need to be sorted, so that when the program wants to look at all reads overlapping position 4,129,888, it can easily find them all at once without having to search through the entire BAM file.
Convert from SAM to BAM format.
Sort and index the BAM file.
What new files were created by these commands? Why didn't we name the output
SRR030257.sorted.bam? Can you guess what a *.bai file is?
Hint: You might be tempted to
gzip BAM files when copying them from one computer to another. Don't bother! They are already internally compressed, so you won't be able to shrink the file. On the other hand, compressing SAM files will save a fair bit of space.
Output BCF file. This is a binary form of the text Variant Call Format (VCF).
Convert BCF to VCF:
Take a look at this file. It has a nice header explaining what the columns mean.
VCF format has Allele Frequency tags denoted by AF1. Try the following command to see what values we have in our files.
For the data we are dealing with, predictions with an allele frequency not equal to 1 are not really applicable here. (The reference genome is haploid. There aren't any heterozygotes.) How can we remove these lines from the file and continue on?
What does the -v flag do in grep?
Is not practical, since we will lose vital VCF formatting and may not be able to use this file in the future.
Will preserve all lines that don't have a AF1=0 value and is one way of doing this.
Is a way of doing it in-line and not requiring you to make another file.
Calling variants in reads mapped by BWA
Follow the same directions to call variants in the BWA-mapped reads.
Just be sure you don't write over your old files. Maybe create another new directory:
You could also try running all of the commands from inside of the
samtools_bwa directory, just for a change of pace.
Comparing the results of different mappers
Set up a new output directory and copy the respective VCF files to it.
Bedtools is a suite of utility programs that work on a variety of file formats, one of which is conveniently VCF format. Using intersectBed and subtractBed we can find equal and different predictions between mappers.
Finding common mutations.
Finding mutations that are unique for each mapper.
- Which mapper finds more variants?
- Can you figure out how to filter the VCF files on various criteria, like coverage, quality, ... ?
- How many high quality mutations are there in these E. coli samples relative to the reference genome?
Look at how the reads supporting these variants were aligned to the reference genome by continuing the Integrative Genomics Viewer (IGV) tutorial.