Skip to content
SalmonTE is an ultra-Fast and Scalable Quantification Pipeline of Transpose Element (TE) Abundances
Jupyter Notebook Python R
Branch: master
Clone or download
Fetching latest commit…
Cannot retrieve the latest commit at this time.
Type Name Latest commit message Commit time
Failed to load latest commit information.
bin the first commit Aug 1, 2017
example add docopt Aug 1, 2017
reference The major change has been done. Dec 19, 2018
scripts added new references Jan 23, 2018
snakemake Rule 'collect_abundance' for single-read data was ommited. Feb 7, 2019
test Decided to skip non-FASTQ file instead of error. Mar 29, 2019
.gitignore Decided to skip non-FASTQ file instead of error. Mar 29, 2019 Create Jan 13, 2018


Change Logs

  • December 19, 2018: SalmonTE has been updated to 0.4 with some improvements!

    • Regarding #14, now SalmonTE is coupled with the latest version of snakemake, so there is no more directory error. Furthermore, SalmonTE no longer runs with the older version of snakemake, please update the version of the snakemake package.
    • Regarding #22, mappability for each file is now reported. (MAPPING_INFO.csv in the quantification output directory)
    • test function has been improved, and this will give better representations of the data.
    • Running of SalmonTE will not produce massive and enigmatic messages anymore.
  • June 4, 2018: Now SalmonTE supports fq and fq.gz extensions.

  • May 3, 2018: Update README.txt

  • May 2, 2018: A bug fix regarding issue #10

  • January 23, 2018: Added references of Mus musculus(mm) and Danio rerio(dr), added a function users to allow to build a customized index (index mode), and fixed a minor bug.

  • December 25, 2017: Fixed a bug for single-end reads dataset.

  • December 14, 2017: Fixed issue of the macOS. We have figured out there is a problem of old version of snakemake. If you already install the package, and the version is not above 4.0.0 (You can check it with snakemake --version) then please update version with below command: pip3 install snakemake --user --upgrade

  • November 27, 2017: source code of PSB manuscript is out now - our manuscript and response letter.

  • November 21, 2017: Version 0.2 is out, SalmonTE now supports two different type of expressions with --exprtype option. Use --exprtype=TPM if you want to use TPM values for the statistical analysis. If you want to run differential expression analysis, then I highly recommend to use --exprtype=count. Here is the nice answer why.


  • June 5, 2018: Our recent paper about TE in Alzhimer's disease has been published in Cell Reports! Please read the paper to see how SalmonTE was succesfully applied! (Cell Reports Link)

What is SalmonTE?

SalmonTE is an ultra-Fast and Scalable Quantification Pipeline of Transpose Element (TE) Abundances from Next Generation Sequencing Data. It comes with Salmon which is a fast and accurate transcriptome quantification method. You can read the details of the pipeline and an example of real data study in my recent published paper in PSB 2018.

What I need to run SalmonTE? Why I have to use it?

  • You only need to have a set of FASTQ files and phenotype data. Furthermore, SalmonTE automatically decided wether your dataset is paired-ends reads or not.
  • conditions can be a numeric data or a categorical data. Based on the data type of the conditions of each sample, SalmonTE will run differential expression analysis or linear regression.
  • Unlikely other TE analysis tools, SalmonTE gives you various visualized output. It must be helpful to your research.

Requirements & Installation

To use SalmonTE python and R must be installed before running it.

* Note: Currently, running SalmonTE on MacOS has an issue, and we are try to fix it soon. Thus, we recommend to use linux environment to play it.

  • Install python and R packages

For python:

Run following line in your console

pip3 install snakemake docopt pandas --user

For R: Run following lines in R console.

install.packages(c("tidyverse", "scales", "WriteXLS", "BiocManager"))
BiocManager::install("DESeq2", version = "3.8")
  • Clone the repository
git clone
  • Add PATH of SalmonTE to your .bashrc file:
  • Re log-in to terminal or use source command:
source ~/.bashrc


Q. I am using SalmonTE on macOS and salmonTE fails to run on quant mode with error messages:

CalledProcessError in line xx of SOME_PATH:
Command ' set -euo pipefail;  ROOT_OF_SALMON_TE/SalmonTE/salmon/darwin/bin/salmon quant...' returned non-zero exit status 134.

A. You may have a problem to run salmon which is an essential tool for the pipeline. You may install Threading Building Blocks library to solve the problem. If you are using homebrew then please use below command:

brew install tbb

How to use it?

Usage: index [--ref_name=ref_name] (--input_fasta=fa_file) [--te_only] quant [--reference=genome] [--outpath=outpath] [--num_threads=numthreads] [--exprtype=exprtype] FILE... test [--inpath=inpath] [--outpath=outpath] [--tabletype=tabletype] [--figtype=figtype] [--analysis_type=analysis_type] [--conditions=conditions] (-h | --help) --version

    -h --help     Show this screen.
    --version     Show version.

An example of SalmonTE usage with command line

Running the quant mode to collect TE expressions


  • --reference: This will select a reference file, and should the species identifier of your data. We are currently supporting references of those species.
    • hs : Homo Sapiens
    • mm : Mus musculus
    • dm : Drosophila melanogaster
    • dr : Danio rerio
  • --outpath: Path to generate quantification results. If you omit this, SalmonTE_output in the current path, and output will be stored in the path.
  • --exprtype: The type of expression measure, and TPM or count are possible options. If you omit this, then "TPM" is the input of the parameter.
  • --num_threads: This has to be an integer, and this parameter will configure how many threads will use for the parallization.

After you put your parameters, you can put the directory which includes a list of FASTQ files, quant --reference=hs example

Or, you can put the list of files like below. quant --reference=hs example/CTRL_1_R1.fastq.gz example/CTRL_2_R1.fastq.gz          

Running test mode to perform statistical test

Before you run test mode, you should modify control.csv condition.csv file which is stored in the outpath. Here are examples of the proper modifications:

For the differential expression analysis, change the file as below. Important: The control samples has to be labeled as control. Other labels will cause errors.


For the regression analysis,


Once the conditions of every sample has been filled, we can run the test mode like the example commnad-line below:

  • --inpath: This should be the path which contains output of quant mode.
  • --outpath: This will be the path to store all outputs for the mode.
  • --tabletype: The file format of the tables, csv, tsv, and xls are supported. If you omit this, then xls formatted file will be generated.
  • --tabletype: The file format of the figures, png, tiff, jpg, and pdf are supported. If you omit this, then pdf formated files will be generated.
  • --analysis_type: The type of the analysis, and DE (for a differential analysis) or LM (for a linear regression analysis) are possible options. If you omit this, then "DE" is the input of the parameter.
  • --conditions: The list of conditions will be considered when DE has been selected for --analysis_type. The input needs to contain two different conditions (written in non-white space characters) and each condition are separated by ,, and no white-space characters are not allowed for the input. i.e. SalmonTE does not care input such as control , treatment. The first condition of the input will be considered as a normal condition (e.g. healthy condition, wild-type mice) in the study, and the later will be considered as another condition which you are interested (e.g. knock-out mice, treatment). test --inpath=SalmonTE_output --outpath=SalmonTE_statistical_test --tabletype=csv --figtype=png --analysis_type=DE --conditions=control,treatment

How to Cite?

author = {Hyun-Hwan Jeong and Hari Krishna Yalamanchili and Caiwei Guo and Joshua M. Shulman and Zhandong Liu},
title = {An ultra-fast and scalable quantification pipeline for transposable elements from next generation sequencing data},
booktitle = {Biocomputing 2018},
chapter = {},
pages = {168-179},
doi = {10.1142/9789813235533_0016},
URL = {},
eprint = {}
address = 
year = 2017
edition = 
You can’t perform that action at this time.