DNA sequencing theory

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.

Theory and sequencing strategies

Sequencing as a covering problem

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.

Early uses derived from elementary probability theory

The earliest result may be found directly from elementary probability theory. Suppose we model the above process taking and as the fragment length and target length, respectively. The probability of "covering" any given location on the target with one particular fragment is then . (This presumes , which is valid often, but not for all real-world cases.) The probability of a single fragment not covering a given location on the target is therefore , and for fragments. The probability of covering a given location on the target with at least one fragment is therefore

This equation was first used to characterize plasmid libraries,[5] but is may appear in a modified form. For most projects , so that, to a good degree of approximation

where is called the redundancy. Note the significance of redundancy as representing the average number of times a position is covered with fragments. Note also that in considering the covering process over all positions in the target, this probability is identical to the expected value of the random variable , the fraction of the target coverage. The final result,

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.

Lander-Waterman theory

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

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).

Parking strategy

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.

Pairwise end-sequencing

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.

Post Human Genome Project advancements

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.

Various artifacts of large-insert sequencing

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 chance of being covered, as opposed to for interior positions. For , classical Lander–Waterman Theory still gives good predictions, but dynamics change for higher redundancies.

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.

Individual and population sequencing

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.

Metagenomic sequencing

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]

Limitations

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 "chicken and egg" closure problem.

See also

References

  1. ↑ Waterman, Michael S. (1995). Introduction to Computational Biology. Boca Raton: Chapman and Hall/CRC. ISBN 0-412-99391-0.
  2. ↑ Hall, P. (1988). Introduction to the Theory of Coverage Processes. New York: Wiley. ISBN 0-471-85702-5.
  3. ↑ Solomon, H. (1978). Geometric Probability. Philadelphia: Society for Industrial and Applied Mathematics. ISBN 0-898-71025-1.
  4. 1 2 Stevens WL (1939). "Solution to a Geometrical Problem in Probability". Annals of Eugenics. 9: 315–320. doi:10.1111/j.1469-1809.1939.tb02216.x.
  5. ↑ Clarke L, Carbon J (1976). "A colony bank containing synthetic Col-El hybrid plasmids representative of the entire E. coli genome". Cell. 9 (1): 91–99. doi:10.1016/0092-8674(76)90055-6. PMID 788919.
  6. ↑ Lander ES, Waterman MS (1988). "Genomic mapping by fingerprinting random clones: a mathematical analysis". Genomics. 2 (3): 231–239. doi:10.1016/0888-7543(88)90007-9. PMID 3294162.
  7. ↑ Fleischmann RD; et al. (1995). "Whole-genome random sequencing and assembly of haemophilus influenzae Rd". Science. 269 (5223): 496–512. Bibcode:1995Sci...269..496F. doi:10.1126/science.7542800. PMID 7542800.
  8. ↑ Roach JC (1995). "Random subcloning". Genome Research. 5 (5): 464–473. doi:10.1101/gr.5.5.464. PMID 8808467.
  9. ↑ Wendl MC, Waterston RH (2002). "Generalized gap model for bacterial artificial chromosome clone fingerprint mapping and shotgun sequencing". Genome Research. 12 (12): 1943–1949. doi:10.1101/gr.655102. PMC 187573Freely accessible. PMID 12466299.
  10. ↑ Arratia R; et al. (1991). "Genomic mapping by anchoring random clones: a mathematical analysis". Genomics. 11 (4): 806–827. doi:10.1016/0888-7543(91)90004-X. PMID 1783390.
  11. ↑ Port E; et al. (1995). "Genomic mapping by end-characterized random clones: a mathematical analysis". Genomics. 26 (1): 84–100. doi:10.1016/0888-7543(95)80086-2. PMID 7782090.
  12. ↑ Zhang MQ, Marr TG (1993). "Genome mapping by nonrandom anchoring: a discrete theoretical analysis". Proceedings of the National Academy of Sciences. 90 (2): 600–604. Bibcode:1993PNAS...90..600Z. doi:10.1073/pnas.90.2.600.
  13. ↑ Roach JC; et al. (2000). "Parking strategies for genome sequencing". Genome Research. 10 (7): 1020–1030. doi:10.1101/gr.10.7.1020. PMC 310895Freely accessible. PMID 10899151.
  14. ↑ Roach JC, Boysen C, Wang K, Hood L (1995). "Pairwise end sequencing: a unified approach to genomic mapping and sequencing". Genomics. 26 (2): 345–353. doi:10.1016/0888-7543(95)80219-C. PMID 7601461.
  15. ↑ Edwards, A.; Caskey, T. (1991). Closure strategies for random DNA sequencing. 3. A Companion to Methods in Enzymology. pp. 41–47.
  16. ↑ Wendl MC, Barbazuk WB (2005). "Extension of Lander–Waterman Theory for sequencing filtered DNA libraries". BMC Bioinformatics. 6: article 245. doi:10.1186/1471-2105-6-245. PMC 1280921Freely accessible. PMID 16216129.
  17. ↑ Wendl MC (2006). "Occupancy modeling of coverage distribution for whole genome shotgun DNA sequencing". Bulletin of Mathematical Biology. 68 (1): 179–196. doi:10.1007/s11538-005-9021-4. PMID 16794926.
  18. ↑ Wendl MC (2006). "A general coverage theory for shotgun DNA sequencing". Journal of Computational Biology. 13 (6): 1177–1196. doi:10.1089/cmb.2006.13.1177. PMID 16901236.
  19. ↑ Levy S; et al. (2007). "The diploid genome sequence of an individual human". PLoS Biology. 5 (10): article e254. doi:10.1371/journal.pbio.0050254. PMC 1964779Freely accessible. PMID 17803354.
  20. ↑ Wheeler DA; et al. (2008). "The complete genome of an individual by massively parallel DNA sequencing". Nature. 452 (7189): 872–876. Bibcode:2008Natur.452..872W. doi:10.1038/nature06884. PMID 18421352.
  21. 1 2 Wendl MC, Wilson RK (2008). "Aspects of coverage in medical DNA sequencing". BMC Bioinformatics. 9: article 239. doi:10.1186/1471-2105-9-239. PMC 2430974Freely accessible. PMID 18485222.
  22. ↑ Ley TJ; et al. (2008). "DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome". Nature. 456 (7218): 66–72. Bibcode:2008Natur.456...66L. doi:10.1038/nature07485. PMC 2603574Freely accessible. PMID 18987736.
  23. ↑ Wendl MC, Wilson RK (2009). "Statistical aspects of discerning indel-type structural variation via DNA sequence alignment". BMC Genomics. 10: article 359. doi:10.1186/1471-2164-10-359. PMC 2748092Freely accessible. PMID 19656394.
  24. ↑ Wendl MC, Wilson RK (2009). "The theory of discovering rare variants via DNA sequencing". BMC Genomics. 10: article 485. doi:10.1186/1471-2164-10-485. PMC 2778663Freely accessible. PMID 19843339.
  25. ↑ Stanhope SA (2010). "Occupancy modeling maximum contig size probabilities and designing metagenomics experiments". PLoS ONE. 5 (7): article e11652. Bibcode:2010PLoSO...511652S. doi:10.1371/journal.pone.0011652. PMC 2912229Freely accessible. PMID 20686599.
  26. ↑ Wendl MC; et al. (2012). "Coverage theories for metagenomic DNA sequencing based on a generalization of Stevens' theorem". Journal of Mathematical Biology. 67: 1141–1161. doi:10.1007/s00285-012-0586-x. PMID 22965653.
  27. ↑ Hooper SD; et al. (2010). "Estimating DNA coverage and abundance in metagenomes using a gamma approximation". Bioinformatics. 26 (3): 295–301. doi:10.1093/bioinformatics/btp687. PMC 2815663Freely accessible. PMID 20008478.
This article is issued from Wikipedia - version of the 6/13/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.