BRB-SeqTools is a user-friendly pipeline tool that includes many well-known software applications designed to help general scientists preprocess and analyze Next Generation Sequencing (NGS) data. It supports the importing and pre-processing of both RNA-Seq and DNA-Seq data, in either FASTQ or BAM file format. For RNA-Seq data in FASTQ format, Tophat can be used to align the reads to a reference genome. In addition, if sufficient computer memory (>= 32GB) is provided, the user can also choose the STAR aligner to map the reads, which significantly improves the computational speed. BWA-MEM is used to align DNA-Seq data. Variant calling analysis can be conducted on both aligned RNA-Seq and DNA-Seq data using Samtools or GATK Best-Practices pipeline tools. For human tumor data, the Variant Call Format (VCF) files generated by the variant-calling pipeline can be filtered and annotated using the somatic mutation annotation tools included in BRB-SeqTools. These tools utilize ANNOVAR or SnpEff to provide gene annotation (e.g. Gene ID) as well as functional annotation (e.g. synonymous or non-synonymous mutation) for each variant, along with predicted effects (e.g., deleterious) of non-synonymous single-nucleotide variants calculated by popular prediction algorithms such as SIFT and Polyphen-2. Additionally, for RNA-Seq data, gene-level raw count data files can be generated using HTSeq. The raw count data can be read into BRB-ArrayTools for gene expression analysis. Currently, BRB-SeqTools can run in the Linux environment on local physical/virtual machines or on remote servers such as Amazon Cloud. An overview of BRB-SeqTools workflow is shown below.
The hardware requirement may vary depending on the size of data. It is recommended that the machine has at least 64GB RAM and 2TB hard disk space (See FAQ #2). Ubuntu OS itself takes about 4.5 GB hard disk space. BRB-SeqTools and other required software (Tophat2, Bowtie, ...) take less than 800 MB total disk space.
Depending on the machine you have, you can install Ubuntu in different ways. The official installation instruction from Ubuntu provides a step-by-step instruction with screenshots for first-time users.
BRB-SeqTools and some other required components need to be set up before using BRB-SeqTools for the first time.
The downloaded file <seqtools-dl-1.0.tar.gz > will be saved under $HOME/Downloads directory by default.
The tarball can be extracted to the desktop or any other place under your $HOME directory by using either the file manager (called Nautilus in Ubuntu) or a terminal command (use the keyboard shortcut 'Ctrl+Alt+t' to open a terminal).
tar -xzvf seqtools-dl-1.0.tar.gz
This will create a new directory called seqtools-dl. This new directory contains the following files:
SeqTools: GUI version of the application
seqtools_dge/seqtools_vc: CLI version of the application
install.sh: script to 'install' the application icon to the right places
INSTALL: instruction of using <install.sh> script
samples.txt: template of samples.txt (tab-delimited)
samples_gatk.txt: template of samples.txt (tab-delimited) for GATK variant calling
examples.txt: examples of using the seqtools_dge/seqtools_vc programs
icon: folder containing the application icon
code: folder containing scripts required for ANNOVAR/SnpEff
Although it is optional, it is recommended to open a terminal and run
create a desktop shortcut with the application icon. Note that running install.sh requires sudo privileges; check it out
here in FAQ.
To launch the GUI application, you can do one of the following:
SeqToolsfile to launch.
to launch. Don't forget the dot and the forward slash when you run an executable from the current directory!
install.shhas been run once).
Before running NGS data analyses in BRB-SeqTools for the first time, the user needs to install some software applications (such as Bowtie, Tophat2 and Samtools) required by the program, by clicking on "Settings" -> "Tools manager". The software can be downloaded by clicking the "Automatic Setup" button to run an installation script. Alternatively, the user can choose to manually download the required software applications, instead of running the script. The "Automatic Setup" method is recommended for users with limited experience with Linux.
If you wish to use GATK for Variant Calling analysis, you need to manually download and set up the software in BRB-SeqTools because of the GATK license restriction. Here are detailed instructions for downloading GATK.
The "Automatic Setup" method provides an easy way to install the required software with no license restrictions.
Upon clicking the "Automatic Setup" button, a new terminal will show up.
The user will then be prompted to enter a sudo password, and the application will start to
download an installation script
from the internet (which is kept updated) and install the required software.
All the required software is installed under the
Note that if you do not have the sudo password, you need to ask your
system administrator for help. Check it out here in FAQ on how to allow an existing user
to have root privileges.
After the installation is finished, the user will be asked to press the ENTER key to close the terminal.
If the required software has been previously installed, you can click the Browse button to select the directory for each software package. It is assumed HTSeq is available under a global environment so there is no entry for it. After the path of each software package has been specified, users can click the 'OK' button to proceed with the main components in BRB-SeqTools.
Note that the required software only needs to be set up once. The path of each required software package will be remembered by BRB-SeqTools.
You are required to manually download and set up GATK in BRB-SeqTools. Before downloading the software, you need to either sign in with your existing Broad account or create a new one. Here is the link to the sign-in and download web page.
1. Log into your account and download the software to you local machine.
2. Browse for the downloaded GenomeAnalysisTK-3.6.tar.bz2 file. Double-click on the .tar.bz2 file to unzip the GenomeAnalysisTK.jar file.
3. Start BRB-SeqTools and go to "Settings" -> "Tools Manager". Browse for a folder that contains the unzipped GenomeAnalysisTK.jar file. Click the "OK" button to save the change. Now GATK is ready to use with BRB-SeqTools.
Reference genome and annotation files are essential for mapping, creating gene counts and calling variants. Before starting alignment or any data analysis in BRB-SeqTools, the user is required to create a new or select an existing reference genome profile, such that the same genome build can be used consistently throughout a particular analysis procedure. To set up the reference genome profile, the user needs to open BRB-SeqTools, go to "Settings" -> "Reference Genome Profile Manager". Upon selecting the "Create a new profile" option on the profile manager dialog page, two buttons will show up on the right side: "Automatic Setup" and "Manual Setup".
For users who 1) do not have any previously downloaded reference genome files and 2)are planning to use one of the four most common human genome builds (i.e. NCBI_GRCh38, Ensembl_GRCh37, UCSC_hg38 and UCSC_hg19), the "Automatic Setup" option is strongly recommended. After the user selects the genome build, enters the reference genome profile name and browses for the directory to which the files will be downloaded, a terminal will pop up to show the download progress of the files. Depending on the internet speed, it may take a long time to complete the download process. If all the files are downloaded successfully, a profile will be created and saved for future use.
If the user chooses not to use the "Automatic Setup" option to download the required reference genome and annotation files, he/she can manually download the files from the Illumina iGenomes website. The dbSNP database VCF file can be downloaded at ftp://ftp.ncbi.nih.gov/snp/organisms/. For example, a GRCh37 version of the dbSNP VCF file can be downloaded at ftp://ftp.ncbi.nih.gov/snp/organisms/human_9606_b146_GRCh37p13/VCF/ using a web browser. We recommend to download the common_all version of the dbSNP VCF file. After manually downloading all the required reference genome and dbSNP VCF files on his/her computer, one should choose the "Manual Setup" option and browse for the directories/files. A profile will be created and saved for future use by clicking on "save this profile"
There are four major components included in BRB-SeqTools: Alignment, Gene Counting, Variant Calling and Variant Annotation. Upon starting BRB-SeqTools, a GUI interface shows up to let the user enter information required by the software, such as the data and analysis types, the input and output directories, as well as the reference genome profile. The user is also allowed to view or edit a file called "samples.txt", which contains sample information required by the software. After all the required parameters are entered, the user can click the "Run" button to start the analysis of interest.A screenshot of the main GUI interface is shown below.
Some input files are required to run BRB-ArrayTools, such as data files in .fastq or .bam format, reference genome files, as well as a sample information file called "samples.txt". The reference genome files are prepared through the "Reference Genome Profile Setup" procedure. It may take extra steps to prepare data files in .fastq format, and to prepare the "samples.txt" file in required format.
The fastq files can be generated from sequencers or public repositories such as the Sequence Read Archive (SRA). If data is obtained from SRA, the data format is in sra which cannot be directly read into BRB-SeqTools. Therefore a program called fastq-dump needs to be run to convert the data format from sra to fastq. An example of using fastq-dump command is
/opt/SeqTools/bin/sratoolkit.2.3.5-2-ubuntu64/bin/fastq-dump --split-3 SRRXXXXXX.sra
This will create one single file called "SRRXXXXXX.fastq" for single-end data or a pair of files named "SRRXXXXXX_1.fastq" and "SRRXXXXXX_2.fastq" for paired-end data. Note that the above command assumes users have run automatic setup tool to install required software. Fastq-dump program is part of SRA ToolKit. The full path to the fastq-dump depends on the SRAToolKit version. See also FAQ #8.
Before starting to run any analysis with BRB-SeqTools, the user needs to construct a table of sequencing design in a tab-delimited file named "samples.txt". This file has the following requirements:
The header of samples.txt consists of LibraryName, LibraryLayout, fastq1, fastq2,
ReadGroup, and SequencerManufacturer.
Each row represents one sample. The column 'LibraryName' contains a name to uniquely represent the sample.
The 'LibraryLayout' should be PAIRED or SINGLE.
The 'fastq1' column contains the fastq file names. Multiple files can be concatenated by the comma sign.
If the library is paired-end, the 'fastq2' column should be
specified in the same format as the 'fastq1' column. The columns 'ReadGroup' and 'SequencerManufacturer'
are optional and only used if the GATK variant calling method is used. Some common values in the
'SequencerManufacturer' column are ILLUMINA, SLX, SOLEXA, SOLID, 454, LS454, COMPLETE, PACBIO, IONTORRENT, CAPILLARY,
HELICOS, UNKNOWN. No blank space is allowed in this column.
An example of the samples.txt file is given below:
This file can be edited using LibreOffice Calc (similar to Microsoft Excel on Windows OS) on Ubuntu by:
seqtools-dlfolder to your working directory.
If the input files are in the bam format, the header of samples.txt should be LibraryName, BamFile, ReadGroup and SequencerManufacturer.
Each row represents one sample. The column 'LibraryName' contains a name to uniquely represent the sample. 'BamFile' should include the filenames for bam files.
The 'ReadGroup' and 'SequencerManufacturer' columns are optional and only used if the GATK variant call method is used. An example of the samples.txt file looks like:
BRB-SeqTools allows NGS data input in either .fastq or .bam file format. If you have .fastq data files, you need to use an aligner to map the data to a reference genome before proceeding with any further analysis. Three aligners are provided, including Tophat, Spliced Transcripts Alignment to a Reference (STAR) and Burrows-Wheeler Aligner (BWA). If you have RNA-Seq data, you can choose between Tophat and STAR. For DNA-Seq data, BWA is the only aligner included in BRB-SeqTools. Below is a screen shot of the interface containing the three aligner options.
BRB-SeqTools requires the following files to map your .fastq data.
Regardless of which aligner/mapper you use, BRB-SeqTools produces one BAM file for each sample.
One of the most common analyses conducted on RNA-Seq data is to generate the summarized read counts on each gene. BRB-SeqTools utilizes the HTSeq software to conduct gene count analysis.
The following files are required as input (see also Tutorials section)
Note: To get reliable results, you must use the same reference genome profile in gene counting and mapping.
The gene count output file is a zipped file named "counts.zip". It contains the same number of files
as the number of samples.
Each file is named by the sample name plus an extension "count", and
contains a table of read counts for all genes in each sample. There are two columns in the table.
The first column contains gene identifiers such as Ensembl IDs or gene symbols and the second column has count values.
These count table files can be imported into BRB-ArrayTools for gene expression analyses.
Alternatively users can use the
DESeqDataSetFromHTSeqCount() function from the
readDGE() function from the
from Bioconductor to
load count data into an
In addition to the gene count analysis of sequencing data, variant calling analysis is another approach commonly used to analyze both DNA-Seq and RNA-Seq data. In BRB-SeqTools, the user can choose to use Samtools or The Genome Analysis Toolkit (GATK) to conduct variant calling analysis. Below is a screen shot showing the GUI interface with variant calling analysis options.
Before calling variants using Samtools or GATK, the user can choose to use the Picard software to mark duplicated reads. This step is recommended only if the sequencing library is prepared using PCR.
There are two variant calling methods implemented in BRB-SeqTools. One is implemented using the Samtools family tools, including Samtools, BCFtools and HTSlib. This method utilizes the multi-allelic caller implemented in Samtools. The other method is implemented by following the GATK Best Practices workflow and consists of several steps, including Split'N'Trim (for RNA-Seq data only), Realign INDELs, Recalibrate Bases, and Call variants using the GATK HaplotypeCaller.
BRB-SeqTools requires the following files as Input to run variant calling analysis on your data.
BRB-SeqTools calls variants sample by sample and reports variants, including SNPs and INDELs in a VCF file for each sample. For human tumor sample data, the VCF files can be annotated using the Somatic Mutation Annotator included in BRB-SeqTools.
The somatic mutation annotator in BRB-SeqTools is designed for human species only, and is mostly used on human tumor data.
In the somatic mutation annotator tool, two popular variant annotation tools, ANNOVAR and SnpEff, are utilized to annotate variants from one or multiple raw VCF files. This tool takes one or multiple raw VCF files as input, and output for each VCF file a gene list containing nonsynonymous and splicing variants that are not known polymorphisms unless in COSMIC, an annotation table for the detected variants, an annotated VCF file and summary reports. The figure below displays the GUI screenshot for the annotator.
The annotator follows the variant annotation process as shown below:
One can download ANNOVAR from the ANNOVAR website. Please register first, and then follow its instructions to download ANNOVAR. Afterwards, please unzip the downloaded file to a directory with write permission.
SnpEff will be automatically installed in
/opt/SeqTools/bin/snpEff after one has run
"Automatic Setup" in "Settings -> Tools Manager".
There are two ways for users to prepare database files required for running the somatic mutation annotator. One way is to manually download all the required database files including reference genome and COSMIC/dbSNP VCF files. The instruction for downloading these files can be found onThe other way is to automatically download these files by clicking on the three "Download" buttons in the annotator. The folder
variantAnnoDatatbaseunder the user's home directory will be created to keep these files. One must first select a genome build to download all database files by following the instructions below:
Notice that, once these files have been downloaded for each genome build, they will be pre-populated if one genome build is selected. If one has run the variant calling pipeline using one genome build in BRB-SeqTools, the genome reference and dbSNP files will be pre-populated when the same genome build is selected in the annotator. In addition, the annotator will keep the running history associated with each genome build, and these database files will be pre-populated accordingly for each genome build in the history. Please always take a look at the drop-down list for the database files, and select those you prefer.
The annotator takes the following as input. (see also Tutorials section)
Suppose one of the raw VCF files in the directory a user has browsed for is named myExample.vcf, the following files will be generated in the user-specified output directory after running either ANNOVAR or SnpEff:
Please note that the detailed explanation about all column names in the output files such as *_genelist.txt and *_annoTable.txt is available here.
BRB-SeqTools also provides a visualization tool called "Variant Quality Metric Distribution" for users to view the histograms or accumulative proportions of variant quality metrics for variant quality score (QUAL), read depth (DP) or mapping quality (MQ). This tool is designed for the purpose of helping users determine appropriate thresholds for QUAL, DP or MQ for VCF files when running the somatic mutation annotator. Below is a screenshot for the tool:
In the histogram tool, you need to browse for a directory for one or multiple VCF files. Once the directory has been browsed, all the VCF files inside will be automatically loaded into the "Select A Sample" field. Please select one VCF sample of your interest from the drop-down list. Please set the bin size for drawing one histogram. Afterwards, please click on "Draw Histogram For ..." and select Variant Quality (QUAL),Read Depth (DP) or Mapping Quality (MQ), and a histogram and a plot with the accumulative proportion of the selected metric will be shown in the tool. You can save the plots in .pdf, .jpg or .png format by clicking on "Save Histogram As ...". Each time you draw a histogram, it will be shown in a new tab widget. You can select each axis of one plot to move, zoom in, zoom out using your mouse for better visualization.
To help first-time users gain experience to use BRB-SeqTools, we provide two sets of test data including all necessary input files.. In addition, we also provide one step-by-step example on variant annotation analysis on VCF files containing human tumor data.
In BRB-SeqTools, examples of running analysis tools on two small sets of NGS data are provided. If you start BRB-SeqTools and click on "Help", you will see two sub-menu items "Tutorial 1: RNA-Seq" and "Tutorial 2: DNA-Seq". Tutorial 1 contains a subset of RNA-Seq data from GSE11209 along with the genome reference files and a "samples.txt" file for you to download. After clicking on the submenu item, you will see the following dialog form.
You can enter the download directory at your choice and then click on "Download and Open", and it will take less than five minutes to download the test data. A message will pop up to let you know when the download process is finished, and the input spaces at the main GUI interface of BRB-SeqTools will be populated, as shown below. You can simply click the "Run" button to start the analysis. It will not take a long time to finish the process of mapping, gene counting and variant calling.
Similarly, Tutorial 2 contains a small subset of raw DNA-Seq data from GSE48215 along with the required reference genome and the "samples.txt" files, on which the user can conduct variant calling analysis.
We provide here a practical example for running the somatic mutation annotator. In this example, a raw VCF named lungcancer_L400T_raw.vcf was annotated by ANNOVAR and SnpEff, respectively. This VCF file was generated in BRB-SeqTools by running the variant calling analysis over one RNA-Seq dataset (GEO Series Number: GSE81089) collected from a patient labeled as "L400T" with lung cancer. The Tophat2 aligner and Samtools mpileup variant caller were employed, and this VCF file was associated with the genome build of hg38 from the UCSC data source. Below is the step-by-step instruction to run ANNOVAR or SnpEff by the use of lungcancer_L400T_raw.vcf:
If you need to run the SeqTools program in a 'headless' way (without a graphical interface), you can run the command line interface (CLI) version of the programs seqtools_dge and seqtools_vc from a terminal. First open a terminal (keyboard binding is Ctrl+Alt+t) and cd to the directory containing seqtools_dge or seqtools_vc. A full list of arguments can be found by adding '-h' argument after the command:
$ ./seqtools_dge -h Name: seqtools_dge - command line interface for gene counting in RNA-Seq data (companion to GUI version of the BRB-SeqTools program) Usage: seqtools_dge DIRECTORY-NAME [Options] Options: DIRECTORY-NAME Directory containing fastq files -h,--help Show this help message --annotDir <string> Annotation directory --indexDir <string> (optional) Bowtie2 genome index files directory If it is not given, annotDir will be used. --outputDir <string> Output directory --alignMethod <string> (optional) Alignment method (tophat/star) --tophatDir <string> (optional) Tophat directory --starDir <string> (optional) STAR directory --bowtieDir <string> (optional) Bowtie directory --samtoolsDir <string> (optional) Samtools directory -p,--num-threads <integer> (optional) Number of threads for the tophat program Default is the number of hardware threads minus 1 --samples (optional) Alternative file name of
--biowulf <yes/no> (optional) Use NIH/Biowulf machines or not. Default is no. If yes, generated scripts will be tailored to the swarm command used by NIH/Biowulf --createScriptOnly <yes/no> Only create the shell script without running it. Default is no. --checkSoftware <yes/no> (optional) Check if the required software exist or not. Default is yes. -v,--version Display version number $ ./seqtools_vc Name: seqtools_vc - command line interface for variant calling and annotation (companion to GUI version of the BRB-SeqTools program) Usage: seqtools_vc DIRECTORY-NAME [Options] Description: Run variant calling or annotation for next-generation sequencing data. For variant calling, the input is a set of (DNA/RNA-Seq) FASTQ or (aligned) BAM files. For variant annotation, the input is a set of VCF files. The available alignment, variant calling and annotation options can be found in detail below. DIRECTORY-NAME Directory containing fastq/bam/vcf files. -h,--help (optional) Show this help message --inputFormat (optional) Use fastq, bam or vcf as the input file format. Default is fastq. --outputDir <string> Output directory --alignMethod <string> (optional) Alignment method (tophat/star for RNA-Seq, bwa for DNA-Seq) --vcMethod <string> (optional) Variant call method . --markDup <yes/no> (optional) Use Picard to eliminate duplicated reads. Default is yes. --annoMethod <string> (optional) Variant call annotation method --annotDir <string> (optional) Annotation directory --indexDir <string> (optional) Bowtie2 or BWA genome index files directory If it is not given, annotDir will be used. --tophatDir <string> (optional) Tophat directory --bowtieDir <string> (optional) Bowtie directory --starDir <string> (optional) STAR directory --samtoolsDir <string> (optional) Samtools directory -p,--num-threads <integer> (optional) Number of threads for the tophat program Default is the number of hardware threads minus 1 --mem-picard <integer> (optional) Memory in GB for Picard program (mark duplication in variant calling). Default is 20 --realignIndel <yes/no> (optional) Realign indels for GATK variant call. Default is no --indelVcfPath <string> (optional) VCF file with known indels (required for GATK pipeline) If this VCF file is same as the known SNPs VCF file, the indel only VCF file will be generated from the known SNPs (dbSNP VCF only) --recalBaseQual <yes/no> (ooptiona) Recalibrate bases quality score for GATK variant call. Default is no --knownSnpPath <string> (optional) VCF file with known SNPs and small indels (required for GATK pipeline) --dataType <rna/dna> (optional) The data is from DNA-Seq or RNA-Seq (required for GATK pipeline) --annovarDir (optional) ANNOVAR directory --annovarDataDir (optional) ANNOVAR database directory --bcftoolsDir (optional) Bcftools directory --htslibDir (optional) Htslib directory --rawvcf (optional) VCF file for annotation --dbsnp (optional) dbSNP VCF file --cosmic (optional) COSMIC VCF file --dbnsfp (optional) dbNSFP database file --refGenome (optional) Reference genome FASTA file --build (optional) Genome build version --min.qual (optional) Minimum call quality for variant filtering. --min.dp (optional) Minimum number of reads covering or bridging the called positions for variant filtering --min.mq (optional) Minimum mapping quality for variant filtering --rcodeDir (optional) Directory containing R code required for variant call analysis --samples (optional) Alternative file name of --biowulf <yes/no> (optional) Use NIH/Biowulf machines or not. Default is no. If yes, generated scripts will be tailored to the swarm command used by NIH/Biowulf --createScriptOnly <yes/no> (optional) Only create the shell script without running it. Default is no. -v,--version (optional) Display version number
This program was built using GCC. The executable file should be able to run on most x64 Linux distributions.
If you only want to generate shell scripts without running them immediately, you can use the --createScriptOnly yes parameter in seqtools_dge or seqtools_vc. This can be useful in a situation that the scripts should be tweaked before being used; e.g. users want to run scripts through the qsub command in a batch system or on a cloud platform.
/opt/SeqTools/bin, we can type the following in a Linux terminal to find out each software version:
/opt/SeqTools/bin/bowtie2-2.2.1/bowtie2 --version # 2.2.1 /opt/SeqTools/bin/tophat-2.0.11.Linux_x86_64/tophat2 --version # 2.0.11 /opt/SeqTools/bin/bwa-0.7.12 # 0.7.12-r1039 # opt/SeqTools/bin/STAR-2.5.1b # 2.5.1b # opt/SeqTools/bin/picard-tools-1.141 # 1.141 /opt/SeqTools/bin/samtools-0.1.19/samtools # 0.1.19-44428cd java -jar /opt/SeqTools/bin/gatk/GenomeAnalysisTK.jar --version # 3.5-0-g36282e4 /opt/SeqTools/bin/bcftools-1.3/bcftools -v # 1.3 cat /opt/SeqTools/bin/HTSeq-0.6.1/VERSION # 0.6.1 ~/annovar/annotate_variation.pl # 2016-02-01 /opt/SeqTools/bin/sratoolkit.2.3.5-2-ubuntu64/bin/fastq-dump --version # 2.3.5 /opt/SeqTools/bin/FastQC/fastqc -v # 0.10.1 /opt/SeqTools/bin/fastx/bin/fastx_trimmer -h # 0.0.13 java -jar /opt/SeqTools/bin/snpEff/snpEff.jar -version # 4.2 R --version # 3.3.0 pandoc --version # 188.8.131.52
$ ./install.sh [sudo] password for brb: Sorry, user brb is not allowed to execute 'bin/mkdir -p /opt/SeqTools/bin/SeqTools' as root on brb-VirtualBox.A simple solution of adding an existing account with root privileges is to run the following terminal command from an account with root privileges,
sudo adduser brb sudoPS. 1. 'brb' has to be replaced with a real user name which does not have sudo privileges yet. 2. The user needs to log out and log in again to see the effect.
ifconfig eth0where the 'eth0' argument represents the first ethernet adapter. The IP address should have a format XXX.XXX.XXX.XXX. You need to enter the IP address in the 'Host name' entry of a dialog when you create a new connection session on WinSCP.
$ sudo su - \ -c "R -e \"install.packages('rmarkdown', repos='https://cran.rstudio.com/')\""