- 1 Introduction
- 2 Where to Find It
- 3 Building
- 4 Usage
- 5 Input files
- 6 Parameters
- 7 Output files
- 8 Example output
The qplot program is to calculate various summary statistics some of which will be plotted in a pdf file which can be used to assess the sequencing quality for illumina sequencing after mapping reads to the reference genome. The main statistics are empirical Phred scores which was calculated based on the background mismatch rate. By background mismatch rate, it means the rate that sequenced bases are different from the reference genome, EXCLUDING dbSNP positions. Other statistics include GC biases, insert size distribution, depth distribution, genome coverage, empirical Q20 count and so on. An example plot and summary text will follow at the end
Where to Find It
The qplot repository is available both via release downloads and via github.
On github, https://github.com/statgen/qplot, you can both browse and download the qplot source code as well as explore the history of changes.
You can obtain the source either with or without git.
The releases may be available both with and without libStatGen included.
If you do not use the release version that already contains libStatGen, you need to download the library: libStatGen.
If you try to compile qplot and it cannot find libStatGen, it will fail and provide instructions of what to do next:
- if libStatGen is in a different location then expected
- follow the directions to set the path to libStatGen
- if libStatGen is not downloaded and you have git
make libStatGenwill download via git and build libStatGen
- if libStatGen is not downloaded and you don't have git
- See libStatGen
Using Git To Track the Current Development Version
Clone (get your own copy)
You can create your own git clone (copy) using:
git clone https://github.com/statgen/qplot.git
git clone git://github.com/statgen/qplot.git
Either of these commands create a directory called
qplot in the current directory.
cd qplot and compile.
Get the latest Updates (update your copy)
To update your copy to the latest version (a major advantage of using git):
Downloading From GitHub Without Git
If you download the latest code/version, make sure you periodically update it by downloading a newer version.
From github you can download:
- Latest Code (master branch)
- via Website
- Goto: https://github.com/statgen/qplot
- Click on the
Download ZIPbutton on the right side panel.
- via Command Line
- via Website
- Specific Release (via a tag)
After downloading the file, uncompress (unzip/untar) it. The directory created will be named
qplot-<name of version you downloaded>.
After obtaining the qplot repository (either by download or from github), compile the code using:
Object (.o) files are compiled into the
obj directory with a subdirectory
profile for the debugging and profiling objects.
This creates the executable(s) in the
qplot/bin/ directory, the debug executable(s) in the
qplot/bin/debug/ directory, and the profiling executable(s) in the
make install installs the opt binary if you have permission.
make test compiles for opt, debug, and profile and runs the tests (found in the
To see all make options, type
If compilation fails due to warnings being treated as errors, please contact us so we can fix the warnings. As a work-around to get it to compile, you can disable the treatment of warnings as errors by editing libStatGen/general/Makefile to remove
Go to qplot and make will create an executable qplot in the qplot sub-directory. Here is the qplot help page
linux_host > ./qplot The following parameters are available. Ones with "" are in effect: References : --reference [/data/local/ref/karma.ref/human.g1k.v37.umfa], --dbsnp [/home/bingshan/data/db/dbSNP/dbSNP130.UCSC.coordinates.tbl], --gccontent [/home/bingshan/data/db/gcContent/gcContent.hg37.w250.out] Create gcContent file : --create_gc , --winsize  Flag filters : --read1_skip, --read2_skip, --paired_skip, --unpaired_skip Dup and QCFail : --dup_keep, --qcfail_keep Mapping filters : --minMapQuality [0.00] Records to process : --first_n_record [-1] Lanes to process : --lanes  Output files : --plot , --stats , --Rcode  Plot labels : --label , --bamLabel 
Three (3) precomputed files are required. Multiple bam/sam files should be appended after all other parameters.
- The reference genome is the same as karma reference genome. If the index files do not exist, qplot will create the index files using the input reference fasta file.
This file has two columns. First column is the chromosome name wich have to be consistent with the reference created above
Although GC content can be calculated on fly each time, it is much more efficient to load a precomputed GC content from a file. To generate the file, use the following command
qplot --rerefence reference.fa --windowsize winsize --create_gc reference.gc
Note: Before running the qplot, it is critical to check how the chromosome numbers are coded. Some bam file use just numbers, others use chr + numbers. You need to make sure that the chromosome numbers from reference and dbsnp are consistent with the bam file.
Most of command line parameters are self explanatory and some of them are described here
- Flag filter
- By default all reads are processed. If it is desired to check only the first read of a pair, use --read2_skip to ignore the second read. And so on.
- Duplication and QCFile
- By default reads marked as dup and QCFile are ignored but can be retained by
--dup_keep or --qcfail_keep
- Records to process is to try the first n reads to test the bam files and check whether it works.
- Lanes to process
- If the input bam files have more than one lane and only some of them need to be checked, they can be specified by --lanes 1,3,5 whatever the number of lanes needed.
- In order for this to work, the lane info has to be encoded in the read name such that lane number is the second field with the delimit of ":".
- Region list
- If the interest of QA is a list of regions, e.g. exons, this can be achieved by providing a list of region. The regions should be in the form of "chr start end label" each line in the file. In order for this option to work, within each chromosome (contig) the regions have to be sorted by starting position, and also the input bam files have to be sorted.
1 100 500 region_A 1 600 800 region_B 2 100 300 region_C ...
- Plot labels
- Two kinds of labels are enabled. First one is the label for the plot (default is empty), e.g. label on the title of each subplot. Second one is a set of labels for each input bam files, e.g. sample ID (default is numbers 1, 2, ... until the number of input bam files.
--label Run100 --bamLabels s1,s2,s3,s4,s5,s6,s7,s8
- Multiple threading
- Number of concurrent threads running for the input bam files. One bam file will be processed by one thread. Therefore using a number which is dividable by the number of input bam files will make it efficient. One extra thread requires memory about 375Mb on top of around 4Gb memory used to hold reference and GC content file.
There are three (optional) output files.
- --plot qa.pdf
- This is a pdf file containing 2 pages each with 4 figures. If --pages 1 is specified, only page 1 is output. The plot is generated using Rscript.
- --stats qa.stats
- This is a text file containing various summary statistics for each input bam/sam file
- --Rcode qa.R
- This is the R code used for plotting the figures in qa.pdf file. If Rscript is not installed in the system the qplot is run, you can use the qa.R to generate the figures in other machines, or extract plotting data from each run and combine multiple runs together to generate more comprehensive plots.
- Summary statistics text file
TotalReads(e6) 72.94 64.52 74.87 62.25 67.21 MappingRate(%) 97.62 97.51 97.75 97.52 97.35 MapRate_MQpass(%) 97.62 97.51 97.75 97.52 97.35 TargetMapping(%) 45.53 45.51 46.39 45.81 46.23 ZeroMapQual(%) 11.52 11.64 11.77 10.97 11.14 MapQual<10(%) 11.91 12.03 12.17 11.34 11.52 PairedReads(%) 100.00 100.00 100.00 100.00 100.00 ProperPaired(%) 96.14 96.10 96.34 95.60 95.91 MappedBases(e9) 2.11 1.87 2.20 1.82 1.97 Q20Bases(e9) 2.05 1.81 2.13 1.76 1.91 Q20BasesPct(%) 97.12 96.98 96.75 96.90 96.91 MeanDepth 35.08 31.05 36.55 30.30 32.82 GenomeCover(%) 2.10 2.10 2.10 2.09 2.10 EPS_MSE 8.89 6.88 8.50 13.32 6.86 EPS_Cycle_Mean 26.04 25.88 25.86 26.12 25.77 GCBiasMSE 0.04 0.05 0.04 0.07 0.04 ISize_mode 250 250 249 210 250 ISize_medium 271 270 270 260 270 DupRate(%) 3.50 3.79 3.27 4.51 3.56 QCFailRate(%) 0.00 0.00 0.00 0.00 0.00 BaseComp_A(%) 26.3 26.4 26.3 26.8 26.3 BaseComp_C(%) 23.7 23.6 23.7 23.2 23.7 BaseComp_G(%) 23.2 23.0 23.2 22.7 23.1 BaseComp_T(%) 26.8 27.1 26.8 27.3 26.9 BaseComp_O(%) 0.0 0.0 0.0 0.0 0.0