RepeatHMM is a novel computational tool to detect any microsatellites (including trinucleotide repeats in trinucleotide repeat disorders (TRD)) from given long reads for a subject of interests. It is able to accurately estimate estimate expansion counts according to the evaluation performance on both simulation data and real data. It is user friendly and easy to install and use.
Accurate and efficient estimation of repeat counts from long-read sequencing data
Analysis of all types of simple repeats
Prefined models are included for more than 10 well known trinucleotide repeats: AFF2, AR, ATN1, ATXN1, ATXN2, ATXN3, ATXN7, ATXN8OS, CACNA1A, DMPK, FMR1, FXN, HTT, PPP2R2B, TBP
Easy to install and use
RepeatHMM takes a set of reads as input, uses a split-and-align strategy to improve alignments, performs error correction, and leverages a hidden Markov model (HMM) and a peak calling algorithm based on Gaussian mixture model to infer repeat counts. RepeatHMM allows users to specify error parameters of the sequencing experiments, thus automatically producing transition and emission matrices for HMM and allowing the analysis of both PacBio and Oxford Nanopore data.
RepeatHMM was evaluated on both random simulation and PCR-based simulation for long reads containing CAG repeats, and also on real datasets of ATXN3 for SCA3 of ATXN10 for SCA10. The results demonstrated that our tool was able to accurately estimate expansion counts from long reads.
RepeatHMM takes long reads from a subject as input, and can also take a BAM file as input to find more than 10 predefined trinucleotide repeats or a gene given by users, after all reads were well aligned to a reference genome.
git clone https://github.com/WGLab/RepeatHMM
cd RepeatHMM
conda env create -f environment.yml
source activate repeathmmenv
cd bin/RepeatHMM_scripts/UnsymmetricPairAlignment
make
cd ../../../Then, you can use run RepeatHMM by python bin/repeatHMM.py.
Users can try other installation options at here if they have issues in the installation process above.
Please refer to Usage for how to use RepeatHMM.
A simple example to run is given below
wget https://github.com/WGLab/RepeatHMM/releases/download/v2.0.3/SRR5363632.fastq.tar.gz
tar -xvf SRR5363632.fastq.tar.gz
source activate repeathmmenv
python RepeatHMM/bin/repeatHMM.py FASTQinput --repeatName atxn3 --GapCorrection 1 --FlankLength 30 --UserDefinedUniqID sca3_pcr25_raw_test --fastq SRR5363632.fastq --outFolder logfq --Patternfile RepeatHMM/bin/reference_sts/hg38/hg38.predefined.pa --hgfile hg38/hg38.fa --hg hg38 For release history, please visit here. For details, please go here.
If you have any questions/issues/bugs, please post them on GitHub. They would also be helpful to other users.
Please cite the publication below if you use our tool:
Qian Liu, Peng Zhang, Depeng Wang, Weihong Gu and Kai Wang. Interrogating the "unsequenceable" genomic trinucleotide repeat disorders by long-read sequencing. Genome Med. 9(1):65, 2017. doi: 10.1186/s13073-017-0456-7.
Qian Liu, Yao Tong and Kai Wang. Genome-wide detection of short tandem repeat expansions by long-read sequencing. BMC Bioinformatics 21:542 (2020)