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Genome Wide Analytics Studies with regard to structural variations is a key component in phenome association. Here we analyze a family trio of father, mother and children for scientific discovery purpose.
Structural variations, SVs, with size 1 base-pair to several 1000s of base-pairs with their precise breakpoints and single-nucleotide polymorphisms, SNPs, were determined for members of a family of four. The method involved optimal genome assembly and mapping to reference genome.
It is discovered that the mitochondrial DNA is less prone to SVs re-arrangements than SNPs and can possibly have paternal leakage of inheritance or high mutation in maternal inheritance. Sex determination of an individual is found to be strongly confirmed by means of calls of nucleotide bases of SVs to the Y chromosome.
mtDNA inheritance pattern proposes concerns for determining ancestry and divergence between races and species. These in silico techniques for analysis would become such a widespread application that a total transformation of the bio-and-medical industry would go through, as is currently with genome wide analytics and association studies. SVs would serve as fingerprint of an individual contributing to his traits and drug responses, more strongly than SNPs.
KeywordsBioinformatics High performance computing Medical informatics Inheritance
Copy number variations
Mitochondrial deoxyribonucleic acid
Single nucleotide variations
DNA is the blueprint of life, and has codified information of chemical reactions that are responsible to our emotions, to susceptibility to a disease, predisposition to a disease or characteristic traits such as height, voice tone with pitch, color of skin and hair and eyes and so on and so forth. At the same time these features can vary depending on external factors and the variation would be dependent on the feature itself and the external factor. These physical attributes are termed as ‘phenotypes’ and in biomedical relevant context it would be the ‘disease phenotypes’. It is not just the blueprint, or the corresponding genotype, that is the only responsible influencing agent for a certain phenotype to be expressed but many more external factors, consumption, exposure, ingestion, etc., have an impact for the onset of a phenotype. However, by and large, the information in the genotype phase does carry a substantial amount of weightage in terms of dictating the disease phenotype of an individual, and cannot be undermined. Thus, it becomes critical to obtain the DNA sequence and analyze them, for the eventual financial and non-financial impact the findings can be for the patient and other stakeholders in the genomics industry, apart from other curiosity such as ancestry and inheritance that the individual might be generally interested in.
Sequencing is hard, but interpretation of ‘big data’ can be much tougher. Technology and thereby machinery has been advancing rapidly and the cost of associated with it is reducing at a significant pace in the area of sequencing DNA. We once had the standard Sanger sequencing technology about a decade ago, which was used to complete the draft of first human genome sequence. Over the years, the technology advanced to introduce paired end sequences where the sequence can be determined at either end of a fragment and the insert size in between the ends can be roughly known apriori. Though the accuracy of this sequence or the base quality is not always reliable, significant lower cost of this technology can allow multiple sequencing of the region of interest which is also known as sequencing coverage, so as to then take the consensus at a region of interest to determine the sequence. Usually a higher average coverage is preferred, and given the various software tools we have for analysis or assembly, typically the coverage should be above 12× for reasonable reliability. The high false discovery rate of structural variation algorithms even in deeply sequenced individual genomes of the order of 30× average coverage [1, 2] suggests that for lower coverage the problem will be even more to get rid of false positives. Nevertheless, the results with coverage as less as 3-5× also could have a lot of meaningful findings, and could be deployed for several genomes analysis which would make sense on a population wide scale at relatively less cost, such as in the 1000 genomes project.
As an example, if the approximate size of human genome is 3 billion nucleotides, size of the reads is 100 nucleotides, and the total number of reads generated in one run of the sequencer is 0.5 billion nucleotides, then the average coverage is (0.5 billion * 100) / 3 billion, or roughly 17×.
Variations at specific loci in genome have been associated with recurrent genomic rearrangements as well as with a variety of diseases, including color blindness, psoriasis, HIV susceptibility, Crohn’s disease and lupus glomerulonephritis [4, 5, 6, 7, 8, 9]. This only enhances the importance of comprehensive catalogue for genotype and phenotype correlation studies [1, 2, 4, 5, 6, 7, 8, 9] in particular when the rare or multiple variations in gene underlie characteristic or disease susceptibility [10, 11]. Microarrays [12, 13, 14] and sequencing [15, 16, 17, 18] reveal that structural variants (SVs) contribution is significant in characterizing population  and disease  characteristics. Interestingly in particular the HLA domain in chromosome VI of an individual which is the MHC region in humans, would be interesting in being decoded for the variations, as a lesser difference between two individual could imply stronger success possibility of organ transplant. In general, the HLA domain variation would give an insight in immunologic responses. However, we must be careful with the results we get when we call for the variations, as any difference could represent actual difference between the DNA sources, an assembly artifact (clone-induced or computational) or alignment error. With time the sequencing of human genomes now become routine , the spectrum of structural variants and copy number variants (CNVs) has widened to include much smaller events. The important aspect now is to know how genomes vary at large as well as fine scales and by what magnitude does it impact a population in general and an individual in particular. The challenge now is to understand its effects on human disease, characteristic traits and phylogenetic evolutionary clues thus having its large impact in medical and forensic area apart from enriching us of mankind evolutionary history.
There has been several new tools made available which can detect variations without the need for assembling the genome for the individual such as those used in the 1000 Genome Project consortium which finds great applicability in case the coverage of sequences is low  and has so to speak yet have a profound impact at a population level. However, if the sequencing coverage is reasonably higher such as above 12-14× in average so to speak in a comparative sense from the data in 1000 Genome Project, then there is no reason as to why assembling the genome and then mapping to a reference genome to detect variations directly should not be the adopted method. In this article, we share result of the variations detected in a family of four individuals’ viz., father, mother, and two daughters.
The total time for the alignment and extraction of information on a single computing core of 2.6 GHz capacity came out to about 85 wall-clock hours, for each individual assembly. Given that the sequencing technology is expected to improve in the next couple of years not just in the length of the reads at either ends but also in terms of quality of confidence in the letters, future versions of assembly softwares will provide more reliable assembly to be generated and more quickly. It can also be safely assumed looking at the current trend past few years that the cost of sequencing would also be dropping further, which would imply that sequencing with much higher coverage of up to 40× average would become more a routine practice. An important challenge would be requirement of high disk space in order to manage data explosion with simply maintaining the raw data or any intermediate data and downstream results. In order to save disk space, an interesting approach could be to simply store the mis-alignments of the individual genome rather than the whole genome. The whole genome raw data and assembly could be put in tape which are less expensive and yet can store the data reliably. One important aspect that has always been an underpinning concern in most bioinformatics software applications has been disk I/O and interprocessor communication bandwidth in case using any of the tools in parallel mode. Another aspect which is crucial for making prediction is the sensitivity and specificity of the algorithm used. Specificity has been kept as a preferred choice of the mode of operation of the softwares, as then the hypothesis which we make from relational comparison has stronger level of confidence. At the same time, once these tools and approaches are used for routine application, there is no reason why we cannot switch to a sensitive mode of using these tools in order to capture more possibilities of variations, though it will obviously be increasing more false-positive cases.
List of SNPs
List of SVs in A105 family
Further, as observed and stated above, since SVs have higher selection pressure than SNPs for the Y-chromosome, the SVs will serve as a better means for paternal ancestry determination for a relatively longer time-span and the SNPs would serve better candidate to determine paternal ancestry and divergence in a relatively shorter time-span.
With the advent of rapid advancement of technology, coupled with decrease in cost of sequencing, it will not be long when every individual will carry their genome-chip which would be comprising of the set of chromosomal sequences, along with information of SVs and SNPs already determined. Many ventures have already started on this line to tap upon the opportunities that this changing world of medical informatics and genomics has to offer. In fact, this would be a practice which we might want to do early in the life of an individual say within a week after his birth. Let’s say we take it a step further and obtain the DNA sample from the fetus itself, thus being able to do analysis of the baby which is to be born. With the power of prediction and integrating it to powerful relational databases we can tell a-priori as to what are the chances of the baby to be healthy in general. We would be able to predict disease susceptibility of the new born baby as well as characteristic traits a-priori, thereby given an opportunity for the mother to decide whether to have the baby or not, and if so what all things she should be caring about.
Mitochondrial DNA and Y-chromosome DNA has been widely been used to determine maternal and paternal ancestry respectively, such as in a recent findings for Native Americans and Indigenous Altaians . Based on the discoveries above, it can thus be safely concluded that if we continue with ancestry determination by mitochondrial DNA, then SVs would serve as better means to determine ancestry for a longer period than SNPs, as they are relatively more rare events. At the same time the SNPs of the mitochondria would serve as better candidate for the characteristic signature of the individual and can be used to determine ancestry and divergence for a relatively shorter period. Having said that, it would still be proposed that given that there is possibility of mitochondrial DNA to be inherited by father as well, maternal ancestry determination by mtDNA should be rephrased as simply ancestry determination by mtDNA. This will also mean that all the analysis which different scientists across the globe have been conducting so far assuming mtDNA to be totally maternally inherited will need a complete change in the understanding and knowledge generated. As it is confirmed that Y-chromosome is completely paternally inherited, ancestry determination by ‘Y line tests’ as Y-chromosomes are confirmed to be totally inherited from the father is always remain as a good methodology. The SNPs of the whole genome can also be used for generic ancestry and divergence determination.
The study was limited by the fact that there is limit to the length of the NGS reads and the coverage was kept to about 14× only. Although 14× coverage is far higher than the previous studies of 1000 genome project phase 1 which had lower coverage, future similar studies can be conducted with a coverage of a recommendation of 50× if genome assembly approach before analytics is to be deployed. The results of mtDNA analysis seemed to be not affected by these factors as there exists 1000s of copies of mtDNA in the cell anyways.
This research article improves our understanding of human genetics, variations in genome, and inheritance. It provides us with new scopes to fetch relevant information and opens door for many newer technologies to be built based on the discoveries. Though we have made these observation for a single family data, it would be highly unlikely that many such similar experiments would not converge to same discoveries. Nevertheless, it would be worthwhile to conduct population and ethnic or caste based studies and where possible combine it with authentic historical matrimonial records for relational database queries obtaining meaningful results. The discoveries make us more equipped with statistical and robust, efficient and relatively less costly means to derive information such as sex determination, or immunologic response to disease, or success rate of organ transplant, or susceptibility to diseases and possible cure for them. The SVs and SNPs in HLA loci would also serve as a medical transformational method for determining the success of organ transplant for a patient, and predisposition to diseases apriori. With the advent of diploid genomes been made available in future with assemblers being able to generate the diploid assembly as well, our understanding for genetics and disease will enhance further and thereby enable better and more reliable technologies to come in.
The author acknowledge support from the German Research Foundation (DFG) and Universität Leipzig within the program of Open Access Publishing.
The author is thankful to University of Leipzig for meeting the cost of publication.
Availability of data and materials
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All work, idea generation, coding, analysis of results and writing the paper has been done by the first author. All authors read and approved the final manuscript.
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The names of individuals participating in the research were kept anonymous, and their consent was taken for analysis work to be published. No medical outcome of the work was reported.
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