A pipeline for genome size estimation and quality assessment of sequenced genome libraries
GSER is implemented in Bash, and requires no
installation. However, other software that are part of the pipeline are required.
There are 2 required software (R and ntCard), and 3 R libraries required.
-Source page: https://www.r-project.org/
$ wget https://cran.r-project.org/src/base/R-3/R-3.6.3.tar.gz $ tar -xvzf tar -xvzf R-3.6.3.tar.gz $ cd R-3.6.3/ $ ./configure $ make $ sudo make install
Check if installation was correct using
$ R --version R version 3.6.3 (2020-02-29) -- "Holding the Windsock" Copyright (C) 2020 The R Foundation for Statistical Computing Platform: x86_64-pc-linux-gnu (64-bit) R is free software and comes with ABSOLUTELY NO WARRANTY. You are welcome to redistribute it under the terms of the GNU General Public License versions 2 or 3. For more information about these matters see https://www.gnu.org/licenses/.
-Source page: https://github.com/bcgsc/ntCard
$ wget https://github.com/bcgsc/ntCard/archive/v1.1.0.tar.gz $ tar -xvzf v1.1.0.tar.gz $ cd ntCard-1.1.0/ $ ./autogen.sh $ ./configure $ make $ sudo make install
Check if installation was correct using
$ ntcard Version 1.1.0 Written by Hamid Mohamadi. Copyright 2018 Canada's Michael Smith Genome Science Centre
Once R is installed, enter the R command line by typing “R” in a terminal:
$ R R version 3.6.3 (2020-02-29) -- "Holding the Windsock" Copyright (C) 2020 The R Foundation for Statistical Computing Platform: x86_64-pc-linux-gnu (64-bit) R is free software and comes with ABSOLUTELY NO WARRANTY. You are welcome to redistribute it under certain conditions. Type 'license()' or 'licence()' for distribution details. Natural language support but running in an English locale R is a collaborative project with many contributors. Type 'contributors()' for more information and 'citation()' on how to cite R or R packages in publications. Type 'demo()' for some demos, 'help()' for on-line help, or 'help.start()' for an HTML browser interface to help. Type 'q()' to quit R.
Source page: https://www.bioconductor.org/packages/release/bioc/html/ShortRead.html
> if (!requireNamespace("BiocManager", quietly = TRUE)) install.packages("BiocManager") > BiocManager::install("ShortRead")
Source page: https://cran.r-project.org/web/packages/ggplot2/
Source page: https://cran.r-project.org/web/packages/reshape2/
Source page: https://plotly.com/r/getting-started/
Download the GSER tarball, and uncompress it:
$ wget https://github.com/mobilomics/GSER/blob/master/gser_v1.0.6.tar.gz
$ tar -xvzf gser_v1.0.6.tar.gz
Grant execution permissions to the pipeline script:
$ chmod u+x gser_v1.0.6/gser_v1.0.6.sh
For simplicity of use, add the GSER full path to your PATH environment variable. First get the full path:
$ readlink -e gser_v1.0.6/gser_v1.0.6.sh
Then copy the output of the previous command, and add it to the PATH variable:
$ export PATH=$PATH:/path/to/GSER
Once GSER is in your PATH variable, you can execute it as
$ gser_v1.0.6.sh CONFIG THREADS OUTPUTDIR CONFIG : Configuration file in the format described below THREADS : Number of threads to use OUTPUTDIR: Name of the directory in which the results will be stored
The CONFIG file is tab-separated, 2 column, plain text file in the following format
K kmersize1,kmersize2,kmersize3,..,kmersizeN Group1 fullpath to fastqfile Group1 fullpath to another fastqfile Group2 fullpath to fastqfile
Line 1 must have K in the first column, and a
comma-separated list of integer numbers to be used as k-mer sizes
Line 2 and onwards must have a Group specification and then the full path (obtained with readlink -e) to the FASTQ file corresponding to that group
Example CONFIG file for Xenopus laevis genome data available at SRA Study ID SRP071264 (https://trace.ncbi.nlm.nih.gov/Traces/study1/?acc=SRP071264):
K 10,11,12,13,14,15,16,17,18,19,20,30,40,50,60,70,80,90,100,110,120,130,140,150 PE_225 /home/user/SRP071264/SRR3210959_1.fastq PE_225 /home/user/SRP071264/SRR3210959_2.fastq PE_450 /home/user/SRP071264/SRR3210971_1.fastq PE_450 /home/user/SRP071264/SRR3210971_2.fastq PE_900 /home/user/SRP071264/SRR3210972_1.fastq PE_900 /home/user/SRP071264/SRR3210972_2.fastq MP_1500 /home/user/SRP071264/SRR3210973_1.fastq MP_1500 /home/user/SRP071264/SRR3210973_2.fastq MP_4000 /home/user/SRP071264/SRR3210974_1.fastq MP_4000 /home/user/SRP071264/SRR3210974_2.fastq
In this example, Genome Size Estimations will be done for k-mer sizes from 10 to 150, in steps of 10. 5 groups were defined according to the type of library (PE: Paired-End and MP: Mate Pair) and insert size (225, 450, 900 for PE, and 1500, 4000 for MP).
Please send any inquiries about usage and/or bugs to mobilomics(at)gmail.com