Tools for estimating differential enrichment of Transposable Elements and other highly repetitive regions
TEToolkit is composed of two tools, TEpeaks and TEtranscripts, each described in its own section below.
NOTE Both programs rely on specially curated GTF files, which are not packaged with this software due to their size. Please go to our website for instructions to download the curated GTF files.
TEpeak takes ChIP-seq (and similar data) alignment files (BAM or BED), identiifes narrow peaks, and is also able to do differential analysis over peaks of two sets of libraries. It is an extension of MACS by adding the funcionality of taking into account multi-reads, another normalization method, bin correlation, and differential analysis. The differential analysis is performed using DESeq.
TEtranscripts takes RNA-seq (and similar data) and annotates reads to both genes & transposable elements. It then performs differential analysis using DESeq.
Created by Ying Jin, Eric Paniagua, Oliver Tam & Molly Hammell, February 2014
Copyright (C) 2014-2015 Ying Jin, Eric Paniagua, Oliver Tam & Molly Hammell Contact: Ying Jin (email@example.com)
Python: 2.6.x or 2.7.x (not tested in Python 3.x)
pysam: 0.8.2.1 or greater
R: 2.15.x or greater
DESeq: 1.5.x or greater
Download compressed tarball.
Navigate into unpacked directory.
Run the following:
$ python setup.py install
If you want to install locally (e.g. /local/home/usr), run this command instead:
$ python setup.py install --prefix /local/home/usr
NOTE In the above example, you must add
to the PATH variable, and
to the PYTHONPATH variable, where python2.X refers to the python version (e.g. python2.7 if using python version 2.7.x).
usage: TEpeaks -t treatment sample [treatment sample ...] -c control sample [control sample ...] --tinput treatment input --cinput control input -s genome [optional arguments] Required arguments: -t | --treatment [treatment sample 1 treatment sample 2...] _Sample files in group 1 (e.g. treatment/mutant), separated by space_ _Sample files in group 2 (e.g. control/wildtype), separated by space_ --tinput treatment input -s genome (hg: human19, mm: mouse9, dm: dm3) Optional arguments: -c | --control [control sample 1 control sample 2 ...] --cinput control input --format [input file format] Input file format: BAM or BED. DEFAULT: BAM --project [name] Name of this project. DEFAULT: TEpeak_out -p | --padj [pvalue] FDR cutoff for significance. DEFAULT: 1e-5 -n | --norm [normalization] Normalization method : sd (library size), bc (bin correlation). DEFAULT: sd -r | --step step size. DEFAULT: 100 -a | --auto auto detect shiftsize. DEFAULT: False -d | --diff require differential analysis -g | --gap maximum allowed gap. DEFAULT: 1000 -f | --fragsize fragment size. DEFAULT: 200 --lmfold lower bound of fold change for modeling shipsize. DEFAULT: 10 --umfold upper bound of fold change for modeling shiftsize. DEFAULT: 30 --minread minimal reads of a peak. DEFAULT: 5 --mode TE counting mode. 'uniq' consider uniq-reads only. 'multi' distribute to all alignments. DEFAULT: multi --wig generate wiggle file for peaks (normalize to 10 million reads in total(library size)) -h | --help help info
Example Command Lines
TEpeaks --format BAM -t S1.bam --tinput S1input.bam -s mm -n sd --mode multi TEpeaks --format BAM -t S1.bam S2.bam -c C1.bam C2.bam --tinput S1input.bam --cinput C1input.bam -s mm -n sd --diff --mode multi
usage: TEtranscripts -t treatment sample [treatment sample ...] -c control sample [control sample ...] --GTF genic-GTF-file --TE TE-GTF-file [optional arguments] Required arguments: -t | --treatment [treatment sample 1 treatment sample 2...] Sample files in group 1 (e.g. treatment/mutant), separated by space -c | --control [control sample 1 control sample 2 ...] Sample files in group 2 (e.g. control/wildtype), separated by space --GTF genic-GTF-file GTF file for gene annotations --TE TE-GTF-file GTF file for transposable element annotations Optional arguments: *Input/Output options* --format [input file format] Input file format: BAM or SAM. DEFAULT: BAM --stranded [option] Is this a stranded library? (yes, no, or reverse). DEFAULT: yes. --sortByPos Input file is sorted by chromosome position. --project [name] Prefix used for output files (e.g. project name) DEFAULT: TEtranscript_out *Analysis options* --mode [TE counting mode] How to count TE: uniq (unique mappers only) multi (distribute among all alignments). DEFAULT: uniq --minread [min_read] read count cutoff. DEFAULT: 1 -L | --fragmentLength [fragLength] Average length of fragment used for single-end sequencing DEFAULT: For paired-end, estimated from the input alignment file. For single-end, ignored by default. -n | --norm [normalization] Normalization method : DESeq_default (default normalization method of DESeq), TC (total annotated read counts), quant (quantile normalization). DEFAULT: DESeq_default -i | --iteration maximum number of iterations used to optimize multi-reads assignment. DEFAULT: 0 -p | --padj [pvalue] FDR cutoff for significance. DEFAULT: 0.05 -f | --foldchange [foldchange] Fold-change ratio (absolute) cutoff for differential expression. DEFAULT: 1 *Other options* -h | --help Show help message --verbose [number] Set verbose level. 0: only show critical messages 1: show additional warning messages 2: show process information 3: show debug messages DEFAULT: 2 --version Show program's version and exit
NOTE BAM files must be either unsorted or sorted by queryname. If the BAM files are sorted by position, please use the ‘–sortByPos’ option
Example Command Lines
If BAM files are unsorted, or sorted by queryname:
TEtranscripts --format BAM --mode multi -t RNAseq1.bam RNAseq2.bam -c CtlRNAseq1.bam CtlRNAseq.bam --project sample_nosort_test
If BAM files are sorted by coordinates/position:
TEtranscripts --sortByPos --format BAM --mode multi -t RNAseq1.bam RNAseq2.bam -c CtlRNAseq1.bam CtlRNAseq.bam --project sample_sorted_test
Recommendations for TEToolkit input files
TEToolkit can perform transposable element quantification from alignment results (e.g. BAM files) generated from a variety of programs. Given the variety of experimental systems, we could not provide an optimal alignment strategy for every approach. Therefore, we recommend that users identify the optimal parameters for their particular genome and alignment program in order to get the best results.
When optimizing the alignment parameters, we recommend taking these points into consideration:
Allowing sufficient number of multi-mappers during alignment
Most alignment programs provide only 1 alignment per read by default. We recommend reporting multiple alignments per read. We have found that reporting a maximum of 100 alignments per read provides an optimal compromise between the size of the alignment file and recovery of multi-mappers in many genome builds. However, we highly suggest that users optimize this parameter for their particular experiment, as this could significantly improve the quality of transposable element quantification.
Optimizing alignment parameters for non-reference strains
It is common that the specific laboratory strains used in an experiment contains genomic variations not present in the reference strain. While this can be mitigated through allowing mismatches during alignments, certain lab strains (e.g. Drosophila melanogaster) have diverged significantly from the reference genomes. We highly recommend that users should refine their alignment procedures to better account for the expected variations between their lab strains and the reference genome, which will accordingly improve their analysis with TEToolkit. Users can also align to a custom genome build specific to their organism, though they would need GTF annotations for genes and transposable elements that are compatible with their custom genome in order to utilize TEToolkit. Please contact us if you require advice in generating these annotation files.
Specific recommendations when using STAR
STAR utilizes two parameters for optimal identification of multi-mappers –outFilterMultimapNmax and –outAnchorMultimapNmax. The author of STAR recommends that –outAnchorMultimapNmax should be set at twice the value used in –outFilterMultimapNmax, but no less than 50. In our study, we used the same number for both parameters (100), and found negligible differences in identifying multi-mappers. Upon further discussion with the author of STAR, we recommend that setting the same value for –outAnchorMultimapNmax and –outFilterMultimapNmax, though we highly suggest users test multiple values of –outAnchorMultimapNmax to identify the optimal value for their experiment.
Copying & distribution
TEtranscripts and TEpeaks are part of TEToolKit.
TEToolKit is free software: you can redistribute it and/or modify it under the terms of the GNU General Public License as published by the Free Software Foundation, either version 3 of the License, or (at your option) any later version.
This program is distributed in the hope that it will be useful, but WITHOUT ANY WARRANTY; without even the implied warranty of MERCHANTABILITY or FITNESS FOR A PARTICULAR PURPOSE. See the GNU General Public License for more details.
You should have received a copy of the GNU General Public License along with TEToolKit. If not, see this website.
Download the file for your platform. If you're not sure which to choose, learn more about installing packages.
|Filename, size||File type||Python version||Upload date||Hashes|
|Filename, size TEToolkit-1.4.11.tar.gz (82.2 kB)||File type Source||Python version None||Upload date||Hashes View|