{"id":299,"date":"2023-08-10T15:21:22","date_gmt":"2023-08-10T15:21:22","guid":{"rendered":"https:\/\/pediatricbrainfoundation.org\/archive\/new-tool-enhances-search-genetic-mutations\/"},"modified":"2023-08-10T15:21:22","modified_gmt":"2023-08-10T15:21:22","slug":"new-tool-enhances-search-genetic-mutations","status":"publish","type":"page","link":"https:\/\/pediatricbrainfoundation.org\/archive\/new-tool-enhances-search-genetic-mutations\/","title":{"rendered":"New tool enhances the search for genetic mutations"},"content":{"rendered":"
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\u00ab Back to Scientific News<\/a><\/div>\n<\/section><\/div>\n
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New tool enhances the search for genetic mutations<\/h1>\n<\/section><\/div>\n
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\n Monday, August 26, 2013<\/span>  \u00b7  Posted by Arizona State University<\/a> <\/div>\n

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A new software tool known as DeNovoGear, which uses statistical probabilities to help identify mutations and more accurately pinpoint their source and their possible significance for health.<\/div>\n<\/p><\/div>\n<\/div>\n

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Concealed within the vastness of the human genome, (comprised of some 3 billion base pairs), mutations are commonplace. While the majority of these appear to have a neutral effect on human health, many others are associated with diseases and disease susceptibility.
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Reed Cartwright, a researcher at Arizona State University\u2019s Biodesign Institute, along with colleagues at ASU, Washington University and the Wellcome Trust Sanger Institute, Cambridge, UK, report on a new software tool known as DeNovoGear, which uses statistical probabilities to help identify mutations and more accurately pinpoint their source and their possible significance for health.<\/p>\n

Improvements in the accuracy of mutation identification and validation could have a profound impact on the diagnosis and treatment of mutation-related diseases.<\/p>\n

\u201cThese techniques are being considered in two different realms,\u201d Cartwright says. \u201cThe first is for pediatric diseases.\u201d Here, a child with an unusual genetic disease may undergo genomic sequencing to see if the mutations observed have been acquired from the parents or are instead, unique to the child. \u201cWe can identify these mutations and try to detect which gene may be broken,\u201d he says.<\/p>\n

The second application is for cancer research, where tumor tissues are genetically compared with normal tissue. Many now believe that the identification of a specific cancer mutation may eventually permit clinicians to customize a treatment for that tissue type. \u201cWe are developing techniques to allow researchers to make those types of analyses, using advanced, probabilistic methods,\u201d Cartwright says. \u201cWe actually model the whole process.\u201d<\/p>\n

Indeed, the method described provides the first model-based approach for ferreting out certain types of mutations. The group\u2019s research results appear in today\u2019s issue of the journal Nature Methods.<\/p>\n

One of the primary goals in genetics is to accurately characterize genetic variation and the rate at which it occurs. Searching for DNA mutations through genetic sequencing is an important ingredient in this quest, but many challenges exist. The current study focuses on a class of mutations that play a critical role in human disease, namely de novo mutations, which arise spontaneously and are not derived from the genomes of either parent.<\/p>\n

Traditionally, two approaches for identifying de novo mutation rates in humans have been applied, each involving estimates of average mutations over multiple generations. In the first, such rates are measured directly through an estimation of the number of mutations occurring over a known number of generations. In the second, or indirect method, mutation rates are inferred by estimating levels of genetic variation within or between species.<\/p>\n

In the new study, a novel approach is used. The strategy, pioneered in part by Donald Conrad, professor in the Department of Genetics at Washington University School of Medicine and corresponding author of the current study, takes advantage of high throughput genetic sequencing to examine whole genome data in search of de novo mutations.<\/p>\n

\u201cThis collaboration started a few years ago, when Donald and I were both working on mutations for the 1,000 Genomes project,\u201d Cartwright says, referring to an ambitious project to produce a comprehensive map of human variation using next-gen\u00a0sequencing.<\/p>\n

The mutations under study may take the form of either point mutations \u2013 individual nucleotide substitutions, or so-called indel (insertion-deletion) mutations. In the latter case, single nucleotides or nucleotide sequences may be either added or subtracted from the genome.<\/p>\n

While point mutations and indel mutations can both have adverse effects on health, indels are significantly more difficult to identify and verify. They have a strong potential to cause havoc when they occur in coding portions of the genome, as the addition or deletion of nucleotides can disrupt the translation process needed to accurately assemble proteins. (The current study is the first paper to use model-based approaches to detect indel mutations.)<\/p>\n

A seemingly simple approach to pinpointing mutations is to compare sequence data from each parent with sequence data from their offspring. Where changes exist at a given site in the offspring, de novo mutations can be inferred and their potential affect on human health, assessed.<\/p>\n

In reality, such efforts are complicated by a number of potential sources of error, including insufficient sampling of the genome, mistakes in the gene sequencing process and errors of alignment between sequences. The new method uses a probabilistic algorithm to evaluate the likelihood of mutation at each site in the genome, comparing it with actual sequence data.<\/p>\n

Human cells contain two copies of the genome \u2013 one from each parent. For most positions in the genome, the bases from each parent are the same or homozygous, but occasionally, they are different or heterozygous.<\/p>\n

Errors derived from conventional methods can take the form of false negatives, particularly when gene sequencing misses heterozygous sites in the genotype of the child. On the other hand, failure to identify a heterozygous site in one of the parents can lead to a false positive result.<\/p>\n

In the current study, data from the 1,000 genomes project was analyzed using DeNovoGear, with markedly improved accuracy. The technique will assist ongoing efforts to better understand which mutations contribute to sporadic disease or cancer in individuals, the distribution of mutations and their characteristics across populations. \u00a0<\/p>\n

The power of this technique comes from its probabilistic model, which calculates the probability of a de novo mutation at a site based on estimations of mutation rates, sequencing error rate and the initial genetic variation in the population from which the parents arise. This model is able to consider multiple explainations for experimental observations and decide between them. The probabilities are used to indentify candidate loci, which are then evaluated using target resequncing.<\/p>\n

Given adequate data of genetic pedigree, the method is able to distinguish germline from somatic mutations in an automated manner with high accuracy.<\/p>\n

\u201cOur goal is to develop software that will allow researchers and clinicians to estimate a range of mutation types, faster, more accurately and cheaper,\u201d Cartwright says.<\/p>\n

In addition to further refining the DeNovoGear software, Cartwright\u2019s group plans to more closely examine normal human tissue in order to establish rates of somatic mutation. Some of the specific mutations currently associated with cancer for example, may actually be part of normal variability, which appears to be much greater than originally assumed. \u201cNo one has really looked at this at the level we\u2019re interested in.\u201d<\/p>\n


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genome<\/a><\/div>\n
DeNovoGear<\/a><\/div>\n
genetic mutations<\/a><\/div>\n
genetics<\/a><\/div>\n
mutations<\/a><\/div>\n
pediatrics<\/a><\/div>\n
cancer<\/a><\/div>\n
de novo<\/a><\/div>\n
genetic sequencing<\/a><\/div>\n
nucleotide<\/a><\/div>\n
indel mutation<\/a><\/div>\n<\/p><\/div>\n<\/div>\n