A new machine-learning method accurately identifies regions of the human genome that have been duplicated or deleted, known as copy number variants.
These regions are often associated with autism and other neurodevelopmental disorders.
The new method integrates data from several algorithms that attempt to identify copy number variants from exome-sequencing data—high-throughput DNA sequencing of only the protein-coding regions of the human genome. The method could help clinicians provide more accurate diagnoses for genetic diseases.
“Exome sequencing is fast becoming the gold standard for identifying genetic variations in clinical settings because it is faster and less expensive that other methods,” says lead author Santhosh Girirajan, associate professor of biochemistry and molecular biology at Penn State.
“However, current algorithms for identifying copy number variation from exome sequencing data suffer from very high false-positive rates—many of the variants they identify aren’t actually real. With our new method, called ‘CN-Learn,’ around ninety percent of the copy number variants we report are real.”
The human genome generally contains two copies of every gene, one on each member of a chromosome pair. When one cell divides into two, the genome is replicated so that each of the daughter cells gets a full complement of genes. Occasionally, however, errors occur during genome replication that, when present in a sperm or egg cell, can lead to an individual getting more or less than two copies of the gene.
To identify copy number variants from exome-sequencing data, researchers look at the relative amount of DNA sequences produced from each gene. If there is only one copy of a gene present in an individual, they expect to see fewer sequencing reads than if there are two copies, and three copies of a gene would lead to more reads.
It’s not quite that simple, however, because a number of other factors can influence how many sequencing reads are produced from each gene. Researchers have therefore developed several algorithms to try to correctly identify copy number variants from exome-sequencing data. Individually, however, these algorithms are not particularly reliable.
“Generally, the high number of false positives from copy-number-variant algorithms has been dealt with by using multiple algorithms and only counting the variants identified by all the methods—like a Venn diagram,” says first author Vijay Kumar Pounraja, a graduate student. “This approach has multiple drawbacks and limitations, so we decided to develop a new machine-learning method instead.”
CN-Learn integrates data from four different copy-number-variant algorithms, and uses a small set of biologically validated deletions and duplications to learn the signatures of these genomic events.
A machine-learning algorithm called ‘random forest’ facilitates this learning process. The algorithm uses hundreds of decision trees to model the relationship between the genetic context of deletions and duplications and the likelihood they are validated. CN-Learn then uses this model to predict deletions and duplications in other samples without validations.
“Decisions about a patient’s diagnosis and eventual treatment are made based on this information, so it’s incredibly important to get them right,” says Girirajan. “Because of this, we’ve made CN-Learn and all of the necessary supporting programs available to download in one easy package.”
The research appears in the journal Genome Research. Support for the research came from the US National Institutes of Health, the Simons Foundation Autism Research Initiative, and the Penn State Huck Institutes of the Life Sciences.
Source: Penn State
