HeteroGenesis is used to generate genomes for multiple related clones in a heterogeneous tumour, along with a matched germline genome. For each clone and germline sample, it provides FASTA files containing the sequences for each copy of a chromosome in the genome, and files detailing the variants incorporated.
HeteroGenesis can also then be used to combine the variant profiles outputs of each clone to give overall bulk tumour outputs that reflect user defined proportions of each clone in a tumour, and its purity. This is useful, for example, when the user intends to carry out in silico sequencing of each clone and combine the reads to form a bulk tumour dataset.
For more information, see "Simulation of Heterogeneous Tumour Genomes with HeteroGenesis and In Silico Whole Exome Sequencing, Tanner G et al., 2019" - https://academic.oup.com/bioinformatics/advance-article/doi/10.1093/bioinformatics/bty1063/5273483 . Please cite this when using HeteroGenesis.
v1.5 - Improved speed. Allows single chromosome to be processed at a time in varincorp. Bug fixed where deletion indels were allowed to overlap other snvs/indels. (17/02/20)
v1.4 - Known variants taken from vcf file instead of flat files and improved speed when using known variants. Fixed default germline SNV rate and somatic CNV number. (02/01/20)
v1.3 - Bug fixed in freqcalc that caused variant allele frequencies to be calculated incorrectly. (26/03/19)
v1.2 - Allows the user to give lists of SNVs, indels, or CNVs for germline or somatic variants to be taken from. (12/02/19)
v1.1 - Release at paper acceptance. (21/12/18)
Python3 and numpy are required to run HeteroGenesis. Python 3.5.2 and numpy 1.12.0 and 1.12.1 have been tested succesfully with it.
heterogenesis_vargen takes ~6hrs and 5GB RAM on a single thread to run under default parameters, which includes a germline and 2 somatic clones. heterogenesis_varincorp takes ~6hr and 8GB RAM on a single thread to process chr1 of ’clone1’ of this output. This can be run in parallel for all chromosomes and clones.
git clone https://github.com/GeorgetteTanner/HeteroGenesis.git
cd HeteroGenesis/
python setup.py install
Instalation should complete in a few seconds.
HeteroGenesis is implemented in three parts:
The first, heterogenesis_vargen, takes: i) a FASTA genome sequence, ii) a .fai index file for the genome sequence, iii) an optional file containing known germline SNV and InDel locations and minor allele frequencies from dbSNP, and iv) a JSON file containing a set of parameters. It outputs a JSON file with lists of variants for the germline and each clone in the simulated tumour, as well as files containing the order that mutations occurred in each.
The second part, heterogenesis_varincorp is then run, once for each clone, and incorporates the list of variants for a clone into a reference genome. It outputs: i) the FASTA genome sequence (one file for each copy of a chromosome), ii) a VCF file of SNV and InDel positions and frequencies, and iii) a file containing the copy numbers along the genome.
The last part, freqcalc, can then be run to combine outputs from clones to generate bulk tumour outputs. It takes a file containing the proportions of each clone in a tumour, along with the outputs from heterogenesis_varincorp, and outputs equivalent files for the bulk tumour.
heterogenesis_vargen -j example.json
-v/--version : Version
-j/--json : JSON file containing parameters.
heterogenesis_varincorp -j example.json -c clone
-v/--version : Version
-j/--json : JSON file containing parameters (the same file used for heterogenesis_vargen).
-c/--clone : Name of clone to generate genomes for.
-x/--chromosome : Optional - Name of a single chromosome to process. Output files can be combined for multiple chromosomes after running.
freqcalc -c clones.txt -d {directory of heterogenesis_varincorp outputs} -p {prefix} -n {name}
-v/-—version : Version
-c/--clones : File with clone proportions in format: 'clone name' \t 'fraction’.
-d/--directory : Directory containing outputs of heterogenesis_varincorp. This should be the same as what was provided for the ‘directory’ parameter with heterogenesis_varincorp.
-p/--prefix : Prefix of heterogenesis_varincorp output file names. This should be the same as what was provided for the ‘prefix’ parameter with heterogenesis_varincorp.
(If the -x option was used in varincorp to process individual chromosoms separately, the vcf an cnv output files must be combined and chromosome names removed from file names before running freqcalc.)
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Reference Genome: The starting genome sequence, in FASTA format, that variants will be incorporated into.
-
Reference Genome Index: A .fai index file for the reference genome, created with samtools faidx. This should be saved in the same directory as the reference genome.
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dbSNP vcf File: A vcf file of known germline SNVs and InDels from dbSNP (uncompressed). Eg. ftp://[email protected]/bundle/hg38/dbsnp_146.hg38.vcf.gz. This may be filtered for lines containing "CAF" and subsampled to around 20,000,000 lines to reduce disk space or memory requirements if necessary. Fewer lines than this may be used but that will likely start to reduce the effect of more common known SNPs being incorporated more frequently than rarer known SNPs.
-
Parameters File: A JSON file containing run parameters and locations of other inputs. Any parameter that is missing from the file will be set at its default value:
(An example parameters file is provided in the repository - 'example.json')
| Parameter | Description | Default Value |
|---|---|---|
| prefix | String added to output file names. | "" |
| reference | FASTA file containing the sequence of a reference or other input genome. Must have a .fai index file located in the same directory. | Required |
| dbsnp | A vcf file of known germline SNPs and InDels from dbSNP. | none |
| directory | Directory to output all files to. | "./" |
| structure | Structure of clones in the tumour, in the format: “clone1_name, clone1_distance_from_parent, clone1_parent_name, clone2_name, clone2_distance_from_parent, clone2_parent_name…”. All parent clone names must also be listed as a separate clone, ie. if clone2’s parent clone is clone1, then clone1 must also be listed as a clone with a parent clone. The exception to this is when the parent clone is ‘germline’, and this must occur at least once as the parent clone for the root clone of the tumour. Loops in the lineage will cause the program to never end, ie. clone1->clone2->clone3->clone1. Distances from parent clones can be any fraction or number as they are used relative to each other. | "clone1,0.2,germline,clone2,0.8,clone1" |
| snvgermline | Rate of germline SNVs per base. | 0.0014 |
| indgermline | Rate of germline indels per base | 0.00014 |
| cnvrepgermline | Number of germline replication CNVs. | 160 |
| cnvdelgermline | Number of germline deletion CNVs. | 1000 |
| aneuploid | Number of somatic aneuploid events. i.e. replication or deletion of chromosomes. These can either be whole genome duplication or individual chromosome duplication or deletion. Aneuploid events are prevented from deleting all copies of a chromosome. Germline aneuploid events are not available. | 2 |
| wgdprob | Probability that each aneuploid event is a whole-genome duplication. | 0.0 |
| snvsomatic | Rate of somatic SNVs per base. | 0.00001 |
| indsomatic | Rate of somatic indels per base. | 0.000002 |
| cnvrepsomatic | Number of somatic replication CNVs. | 250 |
| cnvdelsomatic | Number of somatic deletion CNVs. | 250 |
| dbsnpsnvproportion | Proportion of germline SNVs taken from dbSNP. | 0.99 |
| dbsnpindelproportion | Proportion of germline InDels taken from dbSNP. | 0.97 |
| chromosomes | List of chromosomes to include in the model. Alternatively, "all" can be given, in which case chromosomes 1-22 will be used. This only works for genomes for which chromosomes are labelled 'chr1','chr2'... (Also note that X and Y are not included with "all") | ”all” |
| givengermlinesnvs, givengermlineindels, givengermlinecnvs, givensomaticsnvs, givensomaticindels, givensomaticcnvs | Used to provide lists of variants for when the user wishes to sample from given variants instead of randomly generating them. See 'examplegivenXXX.txt' files for formatting. Only variants that fit into the genome (eg. not in deleted regions etc. will be used). Note: when a CNV is sampled from a given list, the distinction between replication and deletion CNVs (eg. cnvrepsomatic vs cnvdelsomatic) is ignored and the copy number is instead just taken from the given list. A copy number of 2 on chr1A indicates a 1 copy gain, whereas a copy number of 0 on chr1A indicates a 1 copy deletion. | '' |
| givengermlinesnvsproportion, givengermlineindelsproportion, givengermlinecnvsproportion, givensomaticsnvsproportion, givensomaticindelsproportion, givensomaticcnvsproportion | The proportion of variants taken from given lists. For germline SNVs/InDels the proportion of randomly generated variants is 1-(dbsnpsnvproportion + givengermlinesnvsproportion). | 0.0 |
CNV lengths and copy numbers, and indel lengths are taken from lognormal distributions, that are defined by the mean and variance of the underlying normal distribution. Values from these distributions are then scaled up by a multiplication factor for cnv lengths. Indel length distributions are the same for germline and somatic.
| cnvgermlinemean | Germline CNV length lognormal mean. | -10 |
| cnvgermlinevariance | Germline CNV length lognormal variance | 3 |
| cnvgermlinemultiply | Germline CNV length multiplication factor. | 1000000 |
| cnvsomaticmean | Somatic CNV length lognormal mean. | -1 |
| cnvsomaticvariance | Somatic CNV length lognormal variance. | 3 |
| cnvsomaticmultiply | Somatic CNV length multiplication factor. | 1000000 |
| indmean | Indel length lognormal mean. | -2 |
| indvariance | Indel length lognormal variance. | 2 |
| indmultiply | Indel length multiplication factor. | 1 |
| cnvcopiesmean | CNV copies lognormal mean. | 1 |
| cnvcopiesvariance | CNV copies lognormal variance. | 0.5 |
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Variants File: From heterogenesis_vargen.
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Parameters File: The same JSON file as used for heterogenesis_vargen can be given but only the following parameters are used. These should contain the same values as given for heterogenesis_vargen:
| Parameter | Description | Default Value |
|---|---|---|
| prefix | String added to output file names. | "" |
| reference | FASTA file containing the sequence of a reference or other input genome. Must have a .fai index file located in the same directory. | Required |
| directory | Directory containing the JSON variants file output from heterogenesis_vargen and where output files will be written to. | "./" |
| chromosomes | List of chromosomes included in the model. Alternatively, "all" can be given, in which case chromosomes 1-22 will be used. This only works for genomes for which chromosomes are labelled 'chr1','chr2'... (Also note that X and Y are not included with "all") | ”all” |
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Clones File: File with clone proportions in the format: 'clone name' \t 'fraction’ \n.
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Outputs From heterogenesi_varincorp
- _prefix_varaints.json: A JSON file containing information from a python dictionary in the format: [clone][chromosome][variants, SNV/InDel positions, CNV breakpoints, deleted regions]. This is for use by heterogenesis_varincorp and not intended to be manulally viewed.
- _prefixcloneX_variants.txt: This file lists every variant that occured in the clone.
-
{prefix}{cloneX}cnv.txt: This records the copy number status along the genome, allong with phased major/minor alleles.(Positions are 1 based.)
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{prefix}{cloneX}.vcf: This records the position and variant allele frequency (VAF) for each SNV/InDel, allong with the number of occurences on each copy of a chromosome and the overall copy number at that position.
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{prefix}{cloneX}{chrXX}.fasta: The genome sequence in FASTA format. (One file for each copy of each chromosome.)
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{prefix}{sample}cnv.txt: This records the combined copy number status along the genome, allong with phased major/minor alleles, for the bulk tumour sample.(Positions are 1 based.)
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{prefix}{sample}.vcf: This records the combined position and variant allele frequency (VAF) for each SNV/InDel, allong with the phasing of each variant (ie. if the variant occured on an A or B copy of a chromosome) and the overall copy number at that position, for a bulk tumour sample.
This example demonstrates how to run the entire HeteroGenesis process on test parameters. This limits the simulation to use only chromosomes 21 and 22 in order to reduce run time to a few minutes. For full runs, most parameters can be deleted from the json files and instead ran as defaults.
#Install:
git clone https://github.com/GeorgetteTanner/HeteroGenesis.git
cd HeteroGenesis/
python setup.py install
#EITHER:
#1. If wanting germline variants from dbSNP, download a dbsnp file and filter it to reduce memory requirement.
wget ftp://[email protected]/bundle/hg38/dbsnp_146.hg38.vcf.gz
gunzip dbsnp_146.hg38.vcf.gz | grep "CAF" | gshuf -n 20000000 > dbsnp.hg38.vcf
#OR:
#2. If not wanting to include dbSNP variants, remove the
#'"dbsnp":"./dbsnp.hg38.vcf",' line from example.json
awk '!/dbsnp/' example.json > temp ; mv temp example.json
#Download reference genome (or copy from locally saved reference genome to save time):
wget ftp://[email protected]/bundle/hg38/Homo_sapiens_assembly38.fasta.gz
wget ftp://[email protected]/bundle/hg38/Homo_sapiens_assembly38.fasta.fai
gunzip Homo_sapiens_assembly38.fasta.gz
#make test directory:
mkdir ../test1
cd ../test1
#Run heterogenesis_vargen: ~1min
heterogenesis_vargen -j ../HeteroGenesis/example.json
#Run heterogenesis_varincorp on each clone and germline: ~5min
for clone in clone1 clone2 germline ; do heterogenesis_varincorp -j ../HeteroGenesis/example.json -c ${clone} ; done
#You may then want to merge the outputted fasta files from individual chromosomes within a clone.
#Run freqcalc to create bulk sample variant profiles:
freqcalc -c ../HeteroGenesis/example_clones.txt -d . -p test1 -n sample1
If you want to carry out in silico whole exome or targetted sequencing of the created tumour, this can be achieved with w-Wessim (See https://github.com/GeorgetteTanner/w-Wessim for further details.) Alternatively, many other programs exist for whole genome sequencing.
Once reads have been simulated, the following can be used to create bulk samples:
#Align reads using own pipelines.
#Subsample BAM files in proportions listed in the clones file:
samtools view -b -h -s 0.15 -o germline_0.20.bam germline.bam
samtools view -b -h -s 0.65 -o clone2_0.65.bam clone2.bam
samtools view -b -h -s 0.15 -o clone1_0.15.bam clone1.bam
#Combine subsampled bam files to create bulk data.
samtools merge -c -p example_bulk.bam germline_0.20.bam clone2_0.65.bam clone1_0.15.bam
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