------ This is v3.2.2 ------
MitoHiFi v3.2.2 is a python pipeline distributed under MIT License !
MitoHiFi was first developed to assemble the mitogenomes for a wide range of species in the Darwin Tree of Life Project (DToL)
Find out more Darwin Tree of Life data portal
MitoHiFi is a python workflow that assembles mitogenomes from Pacbio HiFi reads.
With MitoHiFi v3.2 you can start from the raw Pacbio HiFi reads (flag -r) or from the assembled contigs (flag -c). You also need a reference mitochondria sequence in FASTA and GenBank format. We provide an internal script (findMitoReference.py) that can be used to find and download the most closely-related reference genome for your species from NCBI..
The availability of high-quality long reads, such as PacBio HiFi, greatly simplifies the assembly of accurate mitogenomes. However, due to the circular nature of the molecule, mitogenomes are typically assembled redundantly, resulting in multicopy mitogenome contigs. To address this, we have developed a pipeline specifically designed to finalize the assembly and the annotation of the mitogenome. Our pipeline takes into account heteroplasmy, aiming to assemble and annotate all mtDNA variants present in your sample. Among these variants, MitoHiFi selects a representative as the final genome assembly based on several criteria including circularization and gene completeness. Additionally, MitoHiFi provides multiple intermediate outputs such as coverage and annotation plots and a multiple sequence alignment (MSA) of all the variants, which facilitates the analysis of mitochondrial heteroplasmy.
MitoHiFi v3.2 will:
(i) Extract mitochondrial reads and assemble them with hifiasm (using the -r flag) or identify mitochondrial contigs among assembled contigs (using the -c flag).
(ii) Identify and separate NUMTS (Nuclear Mitochondrial DNA Sequences) from genuine mitogenome contigs.
(iii) Generate a circularized, non-redundant, and annotated version of all mitochondrial variants present in your sample.
(iv) Select a representative as the final mitochondrial genome assembly.
(v) Plot an annotation image and a coverage plot of the reads (if initiated with the -r flag).
You can view a diagram illustrating the general MitoHiFi workflow here. For documentation on the behaviour of each script visit here.
Below, we describe the three different ways to install MitoHiFi.
We provide a Docker container for MitoHiFi. The container is built using GitHub Actions and can be obtained by running the following command:
docker pull ghcr.io/marcelauliano/mitohifi:master
Once the container is pulled, you can execute MitoHiFi within Docker. If Docker is not available on your cluster computer, you can use Singularity instead. Different environments may require slightly different Singularity parameters, but a generic Singularity command would be as follows:
singularity exec --bind /path/to/container_directory:/path/to/container_directory docker://ghcr.io/marcelauliano/mitohifi:master mitohifi.py -h
We are unable to create a complete Conda recipe for MitoHiFi due to conflicting Python versions required by different dependencies, making it impossible to coexist within the same Conda environment. However, we provide a partial Conda recipe that installs most of the dependencies. To complete the installation, follow these steps:
- Install MitoFinder and/or MITOS outside of Conda.
- Ensure MitoFinder and/or MITOS are added to the PATH before starting the run. Please note that MitoFinder and/or MITOS should be installed separately and made accessible via the PATH environment variable to ensure their proper integration with MitoHiFi. Once those are installed, do:
#Clone MitoHiFi git repo
git clone https://github.com/marcelauliano/MitoHiFi.git
#create a conda environment with our yml file that is inside MitoHiFi/environment
conda env create -n mitohifi_env -f MitoHiFi/environment/mitohifi_env.yml
Add MitoFinder and/or MITOS to the PATH and then activate your mitohifi_env conda environment.
To run MitoHiFi, do:
(mitohifi_env) python MitoHiFi/src/mitohifi.py -h
This is the least recommended way to install MitoHiFi, but below you will find a list of software that needs to be installed and added to your PATH before installing MitoHiFi. The software versions provided are the latest ones we have tested and confirmed to be working:
- python=3.7
- samtools=1.11
- cd-hit=4.8.1
- minimap2=2.19
- hifiasm=0.19.5
- mafft=7.520
- biopython=1.79
- matplotlib=3.2.2
- dna_features_viewer=3.1.2
- pandas=1.3.5
- bedtools=2.31.0
- pillow=6.2.1
- bcbio-gff=0.7.0
- MitoFinder=v1.4.0
- MITOS=2.1.0
- ncbi-blast+
Once all dependencies are installed and in your PATH, git clone MitoHiFi and execute it:
git clone https://github.com/marcelauliano/MitoHiFi.git
python MitoHiFi/src/mitohifi.py -h
usage: MitoHiFi [-h] (-r <reads>.fasta | -c <contigs>.fasta) -f
<relatedMito>.fasta -g <relatedMito>.gbk -t <THREADS> [-d]
[-a {animal,plant,fungi}] [-p <PERC>] [-m <BLOOM FILTER>]
[--max-read-len MAX_READ_LEN] [--mitos]
[--circular-size CIRCULAR_SIZE]
[--circular-offset CIRCULAR_OFFSET] [-winSize WINSIZE]
[-covMap COVMAP] [-v] [-o <GENETIC CODE>]
required arguments:
-r <reads>.fasta -r: Pacbio Hifi Reads from your species
-c <contigs>.fasta -c: Assembled fasta contigs/scaffolds to be searched
to find mitogenome
-f <relatedMito>.fasta
-f: Close-related Mitogenome is fasta format
-g <relatedMito>.gbk -k: Close-related species Mitogenome in genebank
format
-t <THREADS> -t: Number of threads for (i) hifiasm and (ii) the
blast search
optional arguments:
-d -d: debug mode to output additional info on log
-a {animal,plant,fungi}
-a: Choose between animal (default) or plant
-p <PERC> -p: Percentage of query in the blast match with close-
related mito
-m <BLOOM FILTER> -m: Number of bits for HiFiasm bloom filter [it maps
to -f in HiFiasm] (default = 0)
--max-read-len MAX_READ_LEN
Maximum lenght of read relative to related mito
(default = 1.0x related mito length)
--mitos Use MITOS2 for annotation (opposed to default
MitoFinder
--circular-size CIRCULAR_SIZE
Size to consider when checking for circularization
--circular-offset CIRCULAR_OFFSET
Offset from start and finish to consider when looking
for circularization
-winSize WINSIZE Size of windows to calculate coverage over the
final_mitogenom
-covMap COVMAP Minimum mapping quality to filter reads when building
final coverage plot
-v, --version show program's version number and exit
-o <GENETIC CODE> -o: Organism genetic code following NCBI table (for
mitogenome annotation): 1. The Standard Code 2. The
Vertebrate MitochondrialCode 3. The Yeast
Mitochondrial Code 4. The Mold,Protozoan, and
Coelenterate Mitochondrial Code and the
Mycoplasma/Spiroplasma Code 5. The Invertebrate
Mitochondrial Code 6. The Ciliate, Dasycladacean and
Hexamita Nuclear Code 9. The Echinoderm and Flatworm
Mitochondrial Code 10. The Euplotid Nuclear Code 11.
The Bacterial, Archaeal and Plant Plastid Code 12. The
Alternative Yeast Nuclear Code 13. The Ascidian
Mitochondrial Code 14. The Alternative Flatworm
Mitochondrial Code 16. Chlorophycean Mitochondrial
Code 21. Trematode Mitochondrial Code 22. Scenedesmus
obliquus Mitochondrial Code 23. Thraustochytrium
Mitochondrial Code 24. Pterobranchia Mitochondrial
Code 25. Candidate Division SR1 and Gracilibacteria
Code
To run MitoHiFi, you first need a closely related mitochondrial sequence in both FASTA and GenBank formats. We provide a script that can assist you in retrieving this data from the NCBI database. When provided with the species name you are assembling, the script will search for the nearest available mitochondrial assembly on NCBI. By default, the script looks for an exact match of the species for an available mitochondrial assembly. If an exact match is not found, it continues the search for a phylogenetically close candidate based on NCBI taxonomy.
Using the file ilDeiPorc1.reads.100.fa in our test data as an input example, you would do:
findMitoReference.py --species "Deilephila porcellus" --outfolder /path/to/outputdir --min_length 14000
This command will download OQ694980.1.fasta and OQ694980.1.gb that you should use for flags -f and -g in the main pipeline. Attention: once the NCBI is updated with more mitogenomes, findMitoReference.py might download something else.
Now run MitoHiFi with 4 CPUs (change -t to change CPU numbers):
python mitohifi.py -r MitoHiFi/tests/ilDeiPorc1.reads.100.fa -f OQ694980.1.fasta -g OQ694980.1.gb -t 4 -o 5
To test starting from contigs, you are going to use the file MitoHiFi/test/ilPhaBuce1_contig.fa . For that, first you need to download a reference close to that species. For that, do:
findMitoReference.py --species "Phalera bucephala" --outfolder /path/to/outputdir --min_length 14000
Once the close reference is downloaded, run MitoHiFi:
python mitohifi.py -c MitoHiFi/tests/ilPhaBuce1_contig.fa -f NC_072273.1.fasta -g NC_072273.1.fasta -t 4 -o 5
MitoHifi will produce a series of folders with the results. The main results will be in your working folder and they are:
- final_mitogenome.fasta - the final mitochondria circularized and rotated to start at tRNA-Phe
- final_mitogenome.gb - the final mitochondria annotated in GenBank format.
- final_mitogenome.coverage.png - the sequencing coverage throughout the final mitogenome
- final_mitogenome.annotation.png - the predicted genes throughout the final mitogenome
- contigs_annotations.png - annotation plots for all potential contigs
- coverage_plot.png - reads coverage plot of filtered reads mapped to all potential contigs
- contigs_stats.tsv - containing the statistics of your assembled mitos such as the number of genes, size, whether it was circularized or not, if the sequence has frameshifts and etc...
- shared_genes.tsv - show comparison of annotation between close-related mitogenome and all potential contigs assembled
-
Folder contigs_filtering will contain three outputs:
- parsed_blast.txt
- parsed_blast_all.txt
- contigs_ids.txt
- contigs.blastn - outfmt 6 blast output plus 2 extra columns containing respectively length_of_query and length_of_subject
Columns descriptions of parsed_blast.txt and parsed_blast_all.txt: tab separated files with 4 columns as follows
- qseqid - the ID of your input contigs
- %q_in_match - a percentage of the length of your contig in a blast match with the close related species reference
- leng_query - length of your contig
- s_length - lenght of the close-related mitogenome given
- perc - how much percente the leng_query is in relation to s_length
-
Folder contigs_circularization will contain files related to the circularization of the mito contigs. The most important file is
- all_contigs.circularisationCheck.txt - describes the points of circularization for all contigs. The script is run iteratively until no more circularizatin is found, which will happen when you meet (False, -1, -1). The columns are: the contig id, if it circularises or not (True or False), start coordinate of circularisation, end coordinate of circularisation.
-
Folder potential_contigs will contain a folder for each contig present in parsed_blast.txt. Within each contig folder you will find the circularized and annotated mitosequence for that contig.
-
Folder final_mitogenome_choice will contain a few files, the most important one is
- all_mitogenomes.rotated.aligned.fa - this is an aligment of all the mithocondrial sequences assembled by the pipeline. It is possible you will find heteroplasmy in your sample, in which case you will have more than one version of the final mito presented. The pipeline chooses a final representative by a majority rule, using cdhit-est to cluster sequenvces at a 80% identitty and chosing the largest one in that cluster as the final. If you want to study heteroplasmy of your sample, please investigate the all_mitogenomes.rotated.aligned.fa file further, and all the results in the potential_contigs folder.
-
Folder coverage_mapping will contain bam files for a quick inspection on IGV-like softwares, the most important are:
- HiFi-vs-final_mitogenome.sorted.bam - contains mapping information of filtered HiFi reads against the final mitogenome
- HiFi-vs-potential_contigs.sorted.bam - contains mapping information of HiFi reads against all potential contigs
-
If you run the pipeline with flag -r you will have a further folder called reads_mapping_and_assembly which will contain
- gbk.HiFiMapped.bam.fasta - all reads that mapped to the closely-related mito
- gbk.HiFiMapped.bam.filtered.fasta - mapped reads filtered by size. We remove any reads that are larger than the size of the close-related mito (or as specified by --max-read-len ) as a rough way to filter out numpts
- hifiasm.contigs.fasta - final hifiasm primary and alternate contigs concatenated. This is the file used to find your mitos.
MitoHiFi is still not optmized to assemble a plant mitochondria or chloroplast. But if you have a contig you consider to be one of those, you can use MitoHiFi with the flag -c to finalize your organelle! It will circularize (if that is the case) and annotate, and output statistics for you. To do this, you need to use the parameter -a plant when calling the main script mitohifi.py .
Also, the script findMitoReference.py can now search for a chloroplast instead of a mitochondria. Use flag -t chloroplast
Mitohifi is going to pull possible mito contigs by blasting your contigs with the closely-related mito reference genome. The Default parameter -p is going to chose any contig which has 50% or more of its length in the blast match. This is the default because with invertebrate taxa from the Darwin Tree of Life project we have been seeing that the repetitive portion of the mitogenomes is not very conserved between some taxa. In these cases, a more stringent -p ends up excluding real mito sequences. Nevertheless, if you are working with more conserved taxa - such as mammals and other vertebrates - use higher -p (such as 80 or 90) for better results.
The default annotator for MitoHiFi is MitoFinder, but the user can annotate with MITOS by flagging --mitos while starting a MitoHiFi run.
The user can change -winSize and -covMap parameters to tun the final coverage plots.
When using MitoHiFi, please cite our preprint:
MitoHiFi: a python pipeline for mitochondrial genome assembly from PacBio High Fidelity reads Marcela Uliano-Silva, João Gabriel R. N. Ferreira, Ksenia Krasheninnikova, Darwin Tree of Life Consortium, Giulio Formenti, Linelle Abueg, James Torrance, Eugene W. Myers, Richard Durbin, Mark Blaxter, Shane A. McCarthy bioRxiv 2022.12.23.521667; doi: https://doi.org/10.1101/2022.12.23.521667
and
Please cite MitoFinder if you use the default annotation tool:
- Allio, R, Schomaker‐Bastos, A, Romiguier, J, Prosdocimi, F, Nabholz, B, Delsuc, F. MitoFinder: Efficient automated large‐scale extraction of mitogenomic data in target enrichment phylogenomics. Mol Ecol Resour. 2020; 00: 1– 14. https://doi.org/10.1111/1755-0998.13160
or MITOS:
- M. Bernt, A. Donath, F. Jühling, F. Externbrink, C. Florentz, G. Fritzsch, J. Pütz, M. Middendorf, P. F. Stadler MITOS: Improved de novo Metazoan Mitochondrial Genome Annotation Molecular Phylogenetics and Evolution 2013, 69(2):313-319.
And for tRNAs annotation:
- Laslett, D., & Canbäck, B. (2008). ARWEN: a program to detect tRNA genes in metazoan mitochondrial nucleotide sequences. Bioinformatics, 24(2), 172-175.
For more information on python code and pipeline: mu2@sanger.ac.uk and jf18@sanger.ac.uk
Questions about the Docker container: Marcela Uliano-Silva mu2@sanger.ac.uk
Want to know everything about how to run MitoHiFi for animals, funghi and plants? Why the pipeline stops sometimes? Caveats and best practices? Have a watch here: https://youtube.com/watch?v=1NWHC2zkRmg
