DNA sequencing theory is the broad body of work that attempts to lay analytical foundations for determining the order of specific nucleotides in a sequence of DNA, otherwise known as DNA sequencing. The practical aspects revolve around designing and optimizing sequencing projects (known as "strategic genomics"), predicting project performance, troubleshooting experimental results, characterizing factors such as sequence bias and the effects of software processing algorithms, and comparing various sequencing methods to one another. In this sense, it could be considered a branch of systems engineering or operations research. The permanent archive of work is primarily mathematical, although numerical calculations are often conducted for particular problems too. DNA sequencing theory addresses physical processes related to sequencing DNA and should not be confused with theories of analyzing resultant DNA sequences, e.g. sequence alignment. Publications[1] sometimes do not make a careful distinction, but the latter are primarily concerned with algorithmic issues. Sequencing theory is based on elements of mathematics, biology, and systems engineering, so it is highly interdisciplinary. The subject may be studied within the context of computational biology.
All mainstream methods of DNA sequencing rely on reading small fragments of DNA and subsequently reconstructing these data to infer the original DNA target, either via assembly or alignment to a reference. The abstraction common to these methods is that of a mathematical covering problem.[2] For example, one can imagine a line segment representing the target and a subsequent process where smaller segments are "dropped" onto random locations of the target. The target is considered "sequenced" when adequate coverage accumulates (e.g., when no gaps remain).
The abstract properties of covering have been studied by mathematicians for over a century.[3] However, direct application of these results has not generally been possible. Closed-form mathematical solutions, especially for probability distributions, often cannot be readily evaluated. That is, they involve inordinately large amounts of computer time for parameters characteristic of DNA sequencing. Stevens' configuration is one such example.[4] Results obtained from the perspective of pure mathematics also do not account for factors that are actually important in sequencing, for instance detectable overlap in sequencing fragments, double-stranding, edge-effects, and target multiplicity. Consequently, development of sequencing theory has proceeded more according to the philosophy of applied mathematics. In particular, it has been problem-focused and makes expedient use of approximations, simulations, etc.
The earliest result may be found directly from elementary probability theory. Suppose we model the above process taking
L
G
L/G
L\llG
1-L/G
\left[1-L/G\right]N
N
P=1-\left[1-
| L | |
| G |
\right]N.
This equation was first used to characterize plasmid libraries,[5] but it may appear in a modified form. For most projects
N\gg1
\left[1-
| L | |
| G |
\right]N\sim\exp(-NL/G),
where
R=NL/G
C
E\langleC\rangle=1-e-R,
remains in widespread use as a "back of the envelope" estimator and predicts that coverage for all projects evolves along a universal curve that is a function only of the redundancy.
In 1988, Eric Lander and Michael Waterman published an important paper[6] examining the covering problem from the standpoint of gaps. Although they focused on the so-called mapping problem, the abstraction to sequencing is much the same. They furnished a number of useful results that were adopted as the standard theory from the earliest days of "large-scale" genome sequencing.[7] Their model was also used in designing the Human Genome Project and continues to play an important role in DNA sequencing.
Ultimately, the main goal of a sequencing project is to close all gaps, so the "gap perspective" was a logical basis of developing a sequencing model. One of the more frequently used results from this model is the expected number of contigs, given the number of fragments sequenced. If one neglects the amount of sequence that is essentially "wasted" by having to detect overlaps, their theory yields
E\langlecontigs\rangle=Ne-R.
In 1995, Roach[8] published improvements to this theory, enabling it to be applied to sequencing projects in which the goal was to completely sequence a target genome. Michael Wendl and Bob Waterston[9] confirmed, based on Stevens' method,[4] that both models produced similar results when the number of contigs was substantial, such as in low coverage mapping or sequencing projects. As sequencing projects ramped up in the 1990s, and projects approached completion, low coverage approximations became inadequate, and the exact model of Roach was necessary. However, as the cost of sequencing dropped, parameters of sequencing projects became easier to directly test empirically, and interest and funding for strategic genomics diminished.
The basic ideas of Lander–Waterman theory led to a number of additional results for particular variations in mapping techniques.[10] [11] [12] However, technological advancements have rendered mapping theories largely obsolete except in organisms other than highly studied model organisms (e.g., yeast, flies, mice, and humans).
The parking strategy for sequencing resembles the process of parking cars along a curb. Each car is a sequenced clone, and the curb is the genomic target.[13] Each clone sequenced is screened to ensure that subsequently sequenced clones do not overlap any previously sequenced clone. No sequencing effort is redundant in this strategy. However, much like the gaps between parked cars, unsequenced gaps less than the length of a clone accumulate between sequenced clones. There can be considerable cost to close such gaps.
In 1995, Roach et al.[14] proposed and demonstrated through simulations a generalization of a set of strategies explored earlier by Edwards and Caskey.[15] This whole-genome sequencing method became immensely popular as it was championed by Celera and used to sequence several model organisms before Celera applied it to the human genome. Today, most sequencing projects employ this strategy, often called paired end sequencing.
The physical processes and protocols of DNA sequencing have continued to evolve, largely driven by advancements in bio-chemical methods, instrumentation, and automation techniques. There is now a wide range of problems that DNA sequencing has made in-roads into, including metagenomics and medical (cancer) sequencing. There are important factors in these scenarios that classical theory does not account for. Recent work has begun to focus on resolving the effects of some of these issues. The level of mathematics becomes commensurately more sophisticated.
Biologists have developed methods to filter highly-repetitive, essentially un-sequenceable regions of genomes. These procedures are important for organisms whose genomes consist mostly of such DNA, for example corn. They yield multitudes of small islands of sequenceable DNA products. Wendl and Barbazuk[16] proposed an extension to Lander–Waterman Theory to account for "gaps" in the target due to filtering and the so-called "edge-effect". The latter is a position-specific sampling bias, for example the terminal base position has only a
1/G
L/G
R<1
Modern sequencing methods usually sequence both ends of a larger fragment, which provides linking information for de novo assembly and improved probabilities for alignment to reference sequence. Researchers generally believe that longer lengths of data (read lengths) enhance performance for very large DNA targets, an idea consistent with predictions from distribution models.[17] However, Wendl[18] showed that smaller fragments provide better coverage on small, linear targets because they reduce the edge effect in linear molecules. These findings have implications for sequencing the products of DNA filtering procedures. Read-pairing and fragment size evidently have negligible influence for large, whole-genome class targets.
Sequencing is emerging as an important tool in medicine, for example in cancer research. Here, the ability to detect heterozygous mutations is important and this can only be done if the sequence of the diploid genome is obtained. In the pioneering efforts to sequence individuals, Levy et al.[19] and Wheeler et al.,[20] who sequenced Craig Venter and Jim Watson, respectively, outlined models for covering both alleles in a genome. Wendl and Wilson[21] followed with a more general theory that allowed for an arbitrary number of coverings of each allele and arbitrary ploidy. These results point to the general conclusion that the amount of data needed for such projects is significantly higher than for traditional haploid projects. Generally, at least 30-fold redundancy, i.e. each nucleotide spanned by an average of 30 sequence reads, is now standard.[22] However, requirements can be even greater, depending upon what kinds of genomic events are to be found. For example, in the so-called "discordant read pairs method", DNA insertions can be inferred if the distance between read pairs is larger than expected. Calculations show that around 50-fold redundancy is needed to avoid false-positive errors at 1% threshold.[23]
The advent of next-generation sequencing has also made large-scale population sequencing feasible, for example the 1000 Genomes Project to characterize variation in human population groups. While common variation is easily captured, rare variation poses a design challenge: too few samples with significant sequence redundancy risks not having a variant in the sample group, but large samples with light redundancy risk not capturing a variant in the read set that is actually in the sample group. Wendl and Wilson[24] report a simple set of optimization rules that maximize the probability of discovery for a given set of parameters. For example, for observing a rare allele at least twice (to eliminate the possibility is unique to an individual) a little less than 4-fold redundancy should be used, regardless of the sample size.
Next-generation instruments are now also enabling the sequencing of whole uncultured metagenomic communities. The sequencing scenario is more complicated here and there are various ways of framing design theories for a given project. For example, Stanhope[25] developed a probabilistic model for the amount of sequence needed to obtain at least one contig of a given size from each novel organism of the community, while Wendl et al. reported analysis for the average contig size or the probability of completely recovering a novel organism for a given rareness within the community.[26] Conversely, Hooper et al. propose a semi-empirical model based on the gamma distribution.[27]
DNA sequencing theories often invoke the assumption that certain random variables in a model are independent and identically distributed. For example, in Lander–Waterman Theory, a sequenced fragment is presumed to have the same probability of covering each region of a genome and all fragments are assumed to be independent of one another. In actuality, sequencing projects are subject to various types of bias, including differences of how well regions can be cloned, sequencing anomalies, biases in the target sequence (which is not random), and software-dependent errors and biases. In general, theory will agree well with observation up to the point that enough data have been generated to expose latent biases.[21] The kinds of biases related to the underlying target sequence are particularly difficult to model, since the sequence itself may not be known a priori. This presents a type of Catch-22 (logic) problem.
. Michael Waterman . 1995 . Introduction to Computational Biology . Chapman and Hall/CRC . Boca Raton . 978-0-412-99391-6.