A universal SNP and small-indel variant caller using deep neural networks
Biological functions are determined by genes, and differences in function are determined by mutants, or alleles, of those genes. Determining novel alleles is very important in understanding the genetic variation within a species. For example, most eye colors are determined by different alleles of the gene OCA2. All animals receive one copy of each gene from each of their parents. Mutations of a gene are classified as either homozygous (both copies are the same) or heterozygous (the two copies are different).
Next-generation sequencing is a very popular technique for sequencing, or reading, DNA. Since all genes are encoded as DNA, sequencing is an essential tool for understanding genes. Next-generation sequencing works by reading short sections of DNA of length k, called k-means, and then piecing them together or aligning them to a reference genome. Next-generation sequencing is relatively fast and inexpensive, although it can randomly misidentify some nucleotides, introducing errors. However, NGS reading is errorful and arises from a complex error process depending on various factors.
The process of variant calling is determining novel alleles from sequencing data (typically next-generation sequencing data). Some significant alleles only differ from the “standard” version of a gene by only a single base pair, such as the mutation which causes multiple sclerosis. Therefore it is important to be able to accurately call single nucleotide swaps/polymorphisms (SNPs), insertions, and deletions (indels). Calling SNPs and small indels are technically challenging since it requires a program to be able to distinguish between truly novel mutations and errors in the sequencing data.
Previous approaches usually involve using various statistical techniques, a widely used one is GATK. However, these methods have their weaknesses as some assumptions simply don't hold (i.e. independence assumptions), and it's hard to generalize them to other sequencing technologies.
This paper aims to solve the problem of calling SNPs and small indels using a convolutional neural net by casting the reads as images and classifying whether or not they contain a mutation. It introduces a variant caller called "DeepVarient", which requires no specialized knowledge, but performs better than previous state-of-art methods.
In Figure 1, the DeepVariant workflow overview is illustrated.
Initially, the NGS reads aligned to a reference genome are scanned for candidate variants which are different sites from the reference genome. The read and reference data are encoded as an image for each candidate variant site. Then, trained CNN can compute the genotype likelihoods, (heterozygous or homozygous) for each of the candidate variants (figure1, left box). To train the CNN for image classification purposes, the DeepVariant machinery makes pileup images for a labeled sample with known genotypes. These labeled images and known genotypes are provided to CNN for training, and a stochastic gradient descent algorithm is used to optimize the CNN parameters to maximize genotype prediction accuracy. After the convergence of the model, the final model is frozen to use for calling mutations for other image classification tests (figure1, middle box). For example, in figure 1 (right box), the reference and read bases are encoded into a pileup image at a candidate variant site. CNN using this encoded image computes the genotype likelihoods for the three diploid genotype states of homozygous reference (hom-ref), heterozygous (het) or homozygous alternate (hom-alt). In this example, a heterozygous variant call is emitted, as the most probable genotype here is “het”.
Before the sequencing reads can be fed into the classifier, they must be preprocessed. There are many pre-processing steps that are necessary for this algorithm. These steps represent the real novelty in this technique, by transforming the data in a way that allows us to use more common neural network architectures for classification. The preprocessing of the data can be broken into three main phases: the realignment of reads, finding candidate variants and creating images of the candidate variants.
The realignment of the reads phase of the preprocessing is important in order to ensure the sequences can be properly compared to the reference sequences. First, the sequences are aligned to a reference sequence. Reads that align poorly are grouped with other reads around them to build that section, or haplotype, from scratch. If there is strong evidence that the new version of the haplotype fits the reads well, the reads are re-aligned to it. This process updates the CIGAR (Compact Idiosyncratic Gapped Alignment Report) string, a way to represent the alignment of a sequence to a reference, for each read.
Once the reads are properly aligned, the algorithm then proceeds to find candidate variants, regions in the DNA sequence that may contain variants. It is these candidate variants that will eventually be passed as input to the neural network. To find these, we need to consider each position in the reference sequence independently. Any unusable reads are filtered at this point. This includes reads that are not aligned properly, ones that are marked as duplicates, those that fail vendor quality checks, or whose mapping quality is less than ten. For each site in the genome, we collect all the remaining reads that overlap that site. The corresponding allele aligned to that site is then determined by decoding the CIGAR string, which was updated in the realignment phase, of each read. The alleles are then classified into one of four categories: reference-matching base, reference-mismatching base, insertion with a specific sequence, or deletion with a specific length, and the number of occurrences of each distinct allele across all reads is counted. Read bases are only included as potential alleles if each base in the allele has a quality score of at least 10.
With candidate variants identified, the last phase of pre-processing is to convert these candidate variants into images representing the data. This allows for the use of well established convolutional neural networks for image classification for this specialized problem. Each colour channel is used to store a different piece of information about a candidate variant. The red channel encodes which base we have (A, G, C, or T), by mapping each base to a particular value. The quality of the read is mapped to the green colour channel. And finally, the blue channel encodes whether or not the reference is on the positive strand of the DNA. Each row of the image represents a read, and each column represents a particular base in that read. The reference strand is repeated for the first five rows of the encoded image, in order to maintain its information after a 5x5 convolution is applied. With the data preprocessing complete, the images can then be passed into the neural network for classification.
The neural network used is a convolutional neural network. Although the full network architecture is not revealed in the paper, there are several details which we can discuss. The architecture of the network is an input layer attached to an adapted Inception v2 ImageNet model with nine partitions. The input layer takes as input the images representing the candidate variants and rescales them to 299x299 pixels. The output layer is a three-class Softmax layer initialized with Gaussian random weights with a standard deviation of 0.001. This final layer is fully connected to the previous layer. The three classes are the homozygous reference (meaning it is not a variant), heterozygous variant, and homozygous variant. The candidate variant is classified into the class with the highest probability. The model is trained using stochastic gradient descent with a weight decay of 0.00004. The training was done in mini-batches, each with 32 images, using a root mean squared (RMS) decay of 0.9. For the multiple sequencing technologies experiments, a single model was trained with a learning rate of 0.0015 and momentum 0.8 for 250,000 update steps. For all other experiments, multiple models were trained, and the one with the highest accuracy on the training set was chosen as the final model. The multiple models stem from using each combination of the possible parameter values for the learning rate (0.00095, 0.001, 0.0015) and momentum (0.8, 0.85, 0.9). These models were trained for 80 hours, or until the training accuracy converged.
DeepVariant was trained using data available from the CEPH (Centre d’Etude du Polymorphism Humain) female sample NA12878 and was evaluated on the unseen Ashkenazi male sample NA24385. The results were compared with other most commonly used bioinformatics methods, such as the GATK, FreeBayes22, SAMtools23, 16GT24 and Strelka25 (Table 1). For better comparison, the overall accuracy (F1), recall, precision, and numbers of true positives (TP), false negatives (FN) and false positives (FP) are illustrated over the whole genome.
DeepVariant showed the highest accuracy and more than 50% fewer errors per genome compared to the next best algorithm.
They also evaluated the same set of algorithms using the synthetic diploid sample CHM1-CHM1326 (Table 2).
Results illustrated that the DeepVariant method outperformed all other algorithms for variant calling (SNP and indel) and showed the highest accuracy in terms of F1, Recall, precision and TP.
DeepVariant’s strong performance on human data proves that deep learning is a promising technique for variant calling. Perhaps the most exciting feature of DeepVariant is its simplicity. Unlike other states of the art variant callers, DeepVariant has no knowledge of the sequencing technologies that create the reads, or even the biological processes that introduce mutations. This simplifies the problem of variant calling to preprocessing the reads and training a generic deep learning model. It also suggests that DeepVariant could be significantly improved by tailoring the preprocessing to specific sequencing technologies and/or developing a dedicated CNN architecture for the reads, rather than trying to cast them as images.
The paper presents an interesting method for solving an important problem. Building "images" of reads and running them through a generic image classification CNN seems like a strange approach, and it is interesting that it works well. The biggest issues with the paper are the lack of specific information about how the methods. Some extra information is included in the supplementary material, but there are still some big gaps. In particular:
1. What is the structure of the neural net? How many layers, and what sizes? The paper for ConvNet which is cited does not have this information. We suspect that this might be a trade secret that Google is protecting.
2. How is the realignment step implemented? The paper mentions that it uses a "De-Bruijn-graph-based read assembly procedure" to realign reads to a new haplotype. This is a non-standard step in most genomics workflows yet the paper does not describe how they do the realignment or how they build the haplotypes.
3. How did they settle on the image construction algorithm? The authors provide pseudocode for the construction of pileup images but they do not describe how the decisions for made. For instance, the colour values for different base pairs are not evenly spaced. Also, the image begins with 5 rows of the reference genome.
One thing we appreciated about the paper was their commentary on future developments. The authors make it very clear that this approach can be improved on and provide specific ideas for next steps.
Overall, the paper presents an interesting idea with strong results, but lacks detail in some key pieces of the implementation.
The topic of this project is good but we need to more details of the algorithm. In the neural network part, the details are not enough, Authors should provide a figure to better explain how the model works and the structure of the model. Otherwise we cannot understand how the model works.
4 We probably want more details about how the algorithm was exactly implemented to work for this project. Also, when we are preprocessing the data, if different data have different lengths, shall we add more information or drop some information so they match?
 Hartwell, L.H. et. al. Genetics: From Genes to Genomes. (McGraw-Hill Ryerson, 2014).
 Poplin, R. et. al. A universal SNP and small-indel variant caller using deep neural networks. Nature Biotechnology 36, 983-987 (2018).