Clair - deep neural network based variant caller

\
Contact: Ruibang Luo \
Email: rbluo@cs.hku.hk

Introduction

Clair3 released in May 2021 is the successor of Clair, please try out Clair3 at https://github.com/HKU-BAL/Clair3.

Single-molecule sequencing technologies have emerged in recent years and revolutionized structural variant calling, complex genome assembly, and epigenetic mark detection. However, the lack of a highly accurate small variant caller has limited the new technologies from being more widely used. In this study, we present Clair, the successor to Clairvoyante, a program for fast and accurate germline small variant calling, using single molecule sequencing data. For ONT data, Clair achieves the best precision, recall and speed as compared to several competing programs, including Clairvoyante, Longshot and Medaka. Through studying the missed variants and benchmarking intentionally overfitted models, we found that Clair may be approaching the limit of possible accuracy for germline small variant calling using pileup data and deep neural networks.

This is the formal release of Clair (Clair v2, Dec 2019). You can find the experimental Clair v1 (Jan 2019) at https://github.com/aquaskyline/Clair. The preprint of Clair v2 is available in bioRxiv.

Contents

• What are we working on right now
• What’s new
• Installation
• Quick Demo
• Usage
• What’s new
• Submodule Descriptions
• Download Pretrained Models
• Advanced Guides
• Model Training
• Post Processing

What are we working on right now?

• A full alignment representation for higher performance in the low complexity genomics regions.
• Testing small technics to resolve some complex variants, e.g. a deletion that spans a SNP closely followed.

What’s new?

• 20200831
  • added support for alternative allele “*”. “GetTruth.py” now requires a reference genome as input. You don’t need to change your usage if you use “callVarBam.py” for automatic scripts generation.
• 20200416
  • added two new options for haploid calling, --haploid_precision and --haploid_sensitive (in #24)
  • added a simple after calling solution to handle overlapped variants (in #15)
  • fixed haploid GT output (in #17)
• 20200309
  • an ONT model trained with up to 578-fold coverage HG002 data from The Human Pangenome Reference Consortium is now available in Pretrained Models. The below table shows the biased test results, i.e. testing samples were included in training, thus are not for benchmarking but suggest the performance cap of each model at different coverages. The new model shows significantly improved performance at high coverages.

Installation

Option 1. Bioconda

# make sure channels are added in conda
conda config --add channels defaults
conda config --add channels bioconda
conda config --add channels conda-forge
# create conda environment named "clair-env"
conda create -n clair-env -c bioconda clair
conda activate clair-env
# store clair.py PATH into $CLAIR variable
CLAIR=`which clair.py`
# run clair like this afterwards
python $CLAIR --help

The conda environment has the Pypy3 interpreter installed, but one Pypy3 package intervaltree is still missing. The reason why this is not installed by default is because this is not yet available in any conda repositories. To install the package for Pypy3, after activating the conda environment, please run the following commands:

pypy3 -m ensurepip
pypy3 -m pip install --no-cache-dir intervaltree==3.0.2

Then download the trained models:

# download the trained model for ONT
mkdir ont && cd ont
wget http://www.bio8.cs.hku.hk/clair_models/ont/122HD34.tar
tar -xf 122HD34.tar
cd ../
# download the trained model for PacBio CCS
mkdir pacbio && cd pacbio
wget http://www.bio8.cs.hku.hk/clair_models/pacbio/ccs/15.tar
tar -xf 15.tar
cd ../
# download the trained model for Illumina
mkdir illumina && cd illumina
wget http://www.bio8.cs.hku.hk/clair_models/illumina/12345.tar
tar -xf 12345.tar
cd ../

Option 2. Build an anaconda virtual environment step by step

Please install anaconda using the installation guide at https://docs.anaconda.com/anaconda/install/

# create and activate the environment named clair
conda create -n clair python=3.7
conda activate clair
# install pypy and packages on clair environemnt
conda install -c conda-forge pypy3.6
pypy3 -m ensurepip
pypy3 -m pip install intervaltree==3.0.2
# install python packages on clair environment
pip install numpy==1.18.0 blosc==1.8.3 intervaltree==3.0.2 tensorflow==1.13.2 pysam==0.15.3 matplotlib==3.1.2
conda install -c anaconda pigz==2.4
conda install -c conda-forge parallel=20191122 zstd=1.4.4
conda install -c bioconda samtools=1.10 vcflib=1.0.0 bcftools=1.10.2
# clone Clair
git clone --depth 1 https://github.com/HKU-BAL/Clair.git
cd Clair
chmod +x clair.py
export PATH=`pwd`":$PATH"
# store clair.py PATH into $CLAIR variable
CLAIR=`which clair.py`
# run clair like this afterwards
python $CLAIR --help

Then download the trained models referring to download the trained model in Installation - Option 1

Option 3. Docker

# clone Clair
git clone --depth 1 https://github.com/HKU-BAL/Clair.git
cd Clair
# build a docker image named clair_docker_image
docker build -f ./Dockerfile -t clair_docker_image . # You might need root privilege
# run docker image
docker run -it clair_docker_image # You might need root privilege
# store clair.py PATH into $CLAIR variable
CLAIR=`which clair.py`
# run clair like this afterwards
python $CLAIR --help

Then download the trained models referring to download the trained model in Installation - Option 1

After Installation

To check the version of Tensorflow you have installed:

python -c 'import tensorflow as tf; print(tf.__version__)'

To do variant calling using trained models, CPU will suffice. Clair uses 4 threads by default in callVarBam. The number of threads to be used can be controlled using the parameter --threads. To train a new model, a high-end GPU and the GPU version of Tensorflow is needed. To install the GPU version of tensorflow:

pip install tensorflow-gpu==1.13.2

The installation of the blosc library might fail if your CPU doesn’t support the AVX2 instruction set. Alternatively, you can compile and install from the latest source code available in GitHub with the DISABLE_BLOSC_AVX2 environment variable set.

Quick demo

• Step 1. Install Clair, preferably using Installation - Option 1
• Step 2. Run

conda activate clair-env
mkdir clairDemo
cd clairDemo
wget 'http://www.bio8.cs.hku.hk/clair_models/demo/clairDemo.sh'
bash clairDemo.sh

• Step 3. Check the results using less -S ./training/chr21.vcf

Usage

General usage

CLAIR="[PATH_TO_CLAIR]/clair.py"
# to run a submodule using python
python $CLAIR [submodule] [options]
# to run a Pypy-able submodule using pypy (if `pypy3` is the executable command for Pypy)
pypy3 $CLAIR [submodule] [options]

Setup variables for variant calling commands afterwards

CLAIR="[PATH_TO_CLAIR]/clair.py"                         # e.g. clair.py
MODEL="[MODEL_PATH]"                                     # e.g. [PATH_TO_CLAIR_MODEL]/ont/model
BAM_FILE_PATH="[YOUR_BAM_FILE]"                          # e.g. chr21.bam
REFERENCE_FASTA_FILE_PATH="[YOUR_REFERENCE_FASTA_FILE]"  # e.g. chr21.fa
KNOWN_VARIANTS_VCF="[YOUR_VCF_FILE]"                     # e.g. chr21.vcf

Notes

• Each model has three files model.data-00000-of-00001, model.index, model.meta. Please give the MODEL variable, the prefix model.

Call variants at known variant sites or in a chromosome (using callVarBam)

For whole genome variant calling, please use callVarBamParallel to generate multiple commands that invoke callVarBam on smaller chromosome chucks.

Call variants in a chromosome

# variables
VARIANT_CALLING_OUTPUT_PATH="[YOUR_OUTPUT_PATH]"         # e.g. calls/chr21.vcf (please make sure the directory exists)
CONTIG_NAME="[CONTIG_NAME_FOR_VARIANT_CALLING]"          # e.g. chr21
SAMPLE_NAME="[SAMPLE_NAME]"                              # e.g. HG001
python $CLAIR callVarBam \
--chkpnt_fn "$MODEL" \
--ref_fn "$REFERENCE_FASTA_FILE_PATH" \
--bam_fn "$BAM_FILE_PATH" \
--ctgName "$CONTIG_NAME" \
--sampleName "$SAMPLE_NAME" \
--call_fn "$VARIANT_CALLING_OUTPUT_PATH"
cd "$VARIANT_CALLING_OUTPUT_PATH"

Call variants at known variant sites in a chromosome

# variables
VARIANT_CALLING_OUTPUT_PATH="[YOUR_OUTPUT_PATH]"         # e.g. calls/chr21.vcf (please make sure the directory exists)
CONTIG_NAME="[CONTIG_NAME_FOR_VARIANT_CALLING]"          # e.g. chr21
SAMPLE_NAME="[SAMPLE_NAME]"                              # e.g. HG001
KNOWN_VARIANTS_VCF="[YOUR_VCF_PATH]"                     # e.g. chr21_candidates.vcf
python $CLAIR callVarBam \
--chkpnt_fn "$MODEL" \
--ref_fn "$REFERENCE_FASTA_FILE_PATH" \
--bam_fn "$BAM_FILE_PATH" \
--ctgName "$CONTIG_NAME" \
--sampleName "$SAMPLE_NAME" \
--vcf_fn "$KNOWN_VARIANTS_VCF" \
--call_fn "$VARIANT_CALLING_OUTPUT_PATH" \
cd "$VARIANT_CALLING_OUTPUT_PATH"

Call whole-genome variants in parallel (using callVarBamParallel)

# variables
SAMPLE_NAME="NA12878"
OUTPUT_PREFIX="call/var"                        # please make sure the call/ directory exists
# create command.sh for run jobs in parallel
python $CLAIR callVarBamParallel \
--chkpnt_fn "$MODEL" \
--ref_fn "$REFERENCE_FASTA_FILE_PATH" \
--bam_fn "$BAM_FILE_PATH" \
--threshold 0.2 \
--sampleName "$SAMPLE_NAME" \
--output_prefix "$OUTPUT_PREFIX" > command.sh
# disable GPU if you have one installed
export CUDA_VISIBLE_DEVICES=""
# run Clair with 4 concurrencies
cat command.sh | parallel -j4
# Find incomplete VCF files and rerun them
for i in OUTPUT_PREFIX.*.vcf; do if ! [ -z "$(tail -c 1 "$i")" ]; then echo "$i"; fi ; done | grep -f - command.sh | sh
# concatenate vcf files and sort the variants called
vcfcat ${OUTPUT_PREFIX}.*.vcf | bcftools sort -m 2G | bgziptabix snp_and_indel.vcf.gz

Notes

Parallelization

• callVarBamParallel generates a file of callVarBam commands that can be run in parallel.
• Use GNU parallel to run commands in parallel - parallel -j4 will run four concurrencies in parallel using GNU parallel. We suggest using half the number of available CPU cores.
• An alternative to GNU parallel - If GNU parallel is not installed, please try awk '{print "\""$0"\""}' commands.sh | xargs -P4 -L1 sh -c

  Options

• Haploid Precision Mode - Use --haploid_precision option for haploid samples \
  (output homozygous variants only).
• Haploid Sensitive Mode - Use --haploid_sensitive option for haploid samples \
  (output all variants except variants with genotype 1/2).
• Choosing genome sequences and positions for variant calling - callVarBamParallel by default will generate commands for chromosome {1..22},X,Y (insensible to the “chr” prefix). To call variants in other sequences, you can either input via the option --bed_fn your own BED file with three columns including the target sequence names, starting positions and ending positions, or use the option --includingAllContigs to include all sequences in the input FASTA file. If you work on a non-human sample, please always use a BED file or the --includingAllContigs option to define the sequences you want Clair to work on.
• For more accurate Indel calling - You may consider using the --pysam_for_all_indel_bases option for more accurate Indel results. On Illumina data and PacBio CCS data, the option requires 20% to 50% longer running time. On ONT data, Clair can run up to ten times slower, while the improvement in accuracy is not significant.

  Other considerations

• Setting an appropriate allele frequency cutoff - Please refer to About Setting the Alternative Allele Frequency Cutoff
• Check for incomplete (unfinished) VCF files - Incomplete VCF files happens when ‘out of memory’ or other errors occur. The command in the example finds for a newline at the end of the VCF files, and regenerate the incomplete files.
• Disabling GPU: Clair uses CPU for variant calling - To avoid the tensorflow library from using GPU, CUDA_VISIBLE_DEVICES="" makes GPUs invisible to Clair so it will only use CPU for variant calling. Please notice that unless you want to run commands.sh in serial, you cannot use GPU because one running copy of Clair will occupy all available memory of a GPU. While the bottleneck of callVarBam is at the CreateTensor script, which only runs on CPU, the effect of GPU accelerate is insignificant (roughly just about 15% faster). But if you have multiple GPU cards in your system, and you want to utilize them in variant calling, you may want to split the commands.sh into parts, and run the parts by firstly export CUDA_VISIBLE_DEVICES="$i", where $i is an integer from 0 identifying the ID of the GPU to be used.
• Concatenating results - vcfcat and bgziptabix commands are from vcflib, and are installed by default.

Submodule Descriptions

Submodules in clair/ are for variant calling and model training. Submodules in dataPrepScripts are for data preparation.

For the submodules listed below, you use the -h or --help option for available options.

Pretrained Models

Please download models from here or click on the links below.

Advanced Guides

About Setting the Alternative Allele Frequency Cutoff

Different from model training, in which all genome positions are candidates but randomly subsampled for training, variant calling using a trained model will require the user to define a minimal alternative allele frequency cutoff for a genome position to be considered as a candidate for variant calling. For all sequencing technologies, the lower the cutoff, the lower the speed. Setting a cutoff too low will increase the false positive rate significantly, while too high will increase the false negative rate significantly. \
The option --threshold controls the cutoff in these submodules callVarBam, callVarBamParallel and ExtractVariantCandidates. The suggested cutoff is listed below for different sequencing technologies. A higher cutoff will increase the accuracy of datasets with poor sequencing quality, while a lower cutoff will increase the sensitivity in applications like clinical research. Setting a lower cutoff and further filter the variants by their quality is also a good practice.

Variant quality cutoff selection

ONT data

The variant quality distribution of Clair on ONT data is usually bimodal. The best quality cutoff is usually the valley between two peaks plus 50. The image below shows the quality distribution of the variants in HG002 called using ~50-fold coverage ONT data. The best quality cutoff is 748.

PacBio CCS data

The image below shows the quality distribution of the variants in HG005 called using ~30-fold coverage PacBio CCS data. The best quality cutoff is 143.

Illumina data

The image below shows the quality distribution of the variants in HG002 called using ~60-fold coverage Illumina data. The best quality cutoff is 113.

Clair uses PyPy for speedup

Without a change to the code, using PyPy python interpreter on some tensorflow independent modules such as ExtractVariantCandidates and CreateTensor gives a 5-10 times speed up. Pypy python interpreter can be installed by apt-get, yum, Homebrew, MacPorts, etc. If you have no root access to your system, the official website of Pypy provides a portable binary distribution for Linux. Besides following the conda installation method in Installation, the following is a rundown extracted from Pypy’s website (PyPy3.6 v7.2.0 in this case) on how to install the binaries.

wget https://github.com/squeaky-pl/portable-pypy/releases/download/pypy3.6-7.2.0/pypy3.6-7.2.0-linux_x86_64-portable.tar.bz2
tar -jxf pypy3.6-7.2.0-linux_x86_64-portable.tar.bz2
cd pypy3.6-7.2.0-linux_x86_64-portable/bin
./pypy3 -m pip install -U pip wheel intervaltree
# Use pypy3 as an inplace substitution of python to run pypy-able scripts

To guarantee a good user experience (good speed), pypy must be installed to run callVarBam (call variants from BAM), and callVarBamParallel that generate parallelizable commands to run callVarBam.
Tensorflow is optimized using Cython thus not compatible with pypy3. For the list of scripts compatible to pypy3, please refer to the Submodule Descriptions.

Pypy is an awesome Python JIT interpreter, you can donate to the project.