Open access peer-reviewed chapter

Accelerating DNA Computing via PLP-qPCR Answer Read out to Solve Traveling Salesman Problems

By Fusheng Xiong, Michael Kuby and Wayne D. Frasch

Submitted: October 19th 2019Reviewed: February 7th 2020Published: March 19th 2020

DOI: 10.5772/intechopen.91663

Downloaded: 205


An asymmetric, fully-connected 8-city traveling salesman problem (TSP) was solved by DNA computing using the ordered node pair abundance (ONPA) approach through the use of pair ligation probe quantitative real time polymerase chain reaction (PLP-qPCR). The validity of using ONPA to derive the optimal answer was confirmed by in silico computing using a reverse-engineering method to reconstruct the complete tours in the feasible answer set from the measured ONPA. The high specificity of the sequence-tagged hybridization, and ligation that results from the use of PLPs significantly increased the accuracy of answer determination in DNA computing. When combined with the high throughput efficiency of qPCR, the time required to identify the optimal answer to the TSP was reduced from days to 25 min.


  • DNA computing
  • traveling salesman problem
  • ordered node pair abundance
  • pair ligation probe-qPCR
  • PLP-qPCR

1. Introduction

The traveling salesman problem (TSP) computes the shortest route on the arcs of a network that visits a given set of nodes (cities) before returning to the starting point [1, 2, 3, 4, 5, 6]. In many cases, in silico computers are incapable of quickly determining an exact solution of these nondeterministic polynomial (NP) problems because a linear increase in the number of variables leads to a factorial increase in the number of potential solutions. Although advanced heuristic methods have increased the ability of in silico computers to provide approximate answers to NP problems [7], they lack the massive parallelism and data storage required to find exact solutions. DNA computing, which uses the hybridization of DNA molecules as a means to make computations [8, 9, 10, 11, 12, 13, 14, 15], is particularly well-suited to solve computationally intense NP problems such as the TSP because multiple sequences of DNA in a solution can hybridize simultaneously, thereby performing massively parallel computing.

Several technical limitations have prevented DNA computing from reaching its full potential. Although the computation can occur within seconds, current applications of DNA computing are largely limited by time-consuming and labor-intensive answer sorting and determination processes. For example, a gradient PCR procedure that involved a series of PCR reactions with a variety of primer pair combinations was used to determine the solution to a 7-city directed Hamiltonian circuit problem [8]. Other answer determination methods include DNA sequencing [16], and denaturation temperature gradient-polymerase chain reaction (DTG-PCR) associated with denaturing gradient gel electrophoresis (DGGE) and/or temperature gradient gel electrophoresis (TGGE) [10, 17, 18]. Neither DNA sequencing nor DGDC/TGDC can be used to identify the optimal answer to a TSP because the feasible answers represent both optimal and suboptimal answers that differ only in the order in which the components were ligated when the answers were formed, and are flanked by the sequences that encode the start and end nodes. The dependence of the discriminatory powers of DTG-PCR, DGGE, and TGGE on the diversity of oligonucleotide components, especially the G and C content [19, 20] also limits their applicability for answer determination of NP-complete problems.

Xiong et al. [12] developed the ordered node pair abundance (ONPA) approach to identify the optimal answer of an asymmetric, fully-connected 15-city TSP, the largest problem solved to date, using DNA computing. In that study, 20-mer DNA sequences that specifically encoded the nodes and arcs in the network were added to the reaction mixture in the presence of ligase. The sequence of each arc was capable of linking two node sequences in a specific order via hybridization of the last 10 bases of the prior node to the first 10 bases of the subsequent node. The efficiency of each arc in the network was encoded as the concentration of DNA for that arc using saturating concentrations of DNA for each node. Ligation of these sequences then formed covalently linked ordered node pairs (ONPs) that assembled into answer sequences representing tours through the network, such that the optimal answer would be formed in greatest abundance.

The optimal answer to the 15-city TSP was identified by ONPA after infeasible answer sequences were removed by electrophoresis and magnetic bead separation [11, 12]. For each ONP examined by ONPA, probes were designed to hybridize to the 3′-end of the prior node and the 5′-end of the subsequent node in the ordered pair as well as a complementary pair for use in ligation chain reaction (LCR). Each pair of probes was then subjected to the same number of LCR cycles in the presence of an aliquot of answer sequences, and the relative abundance of LCR product was quantified by PAGE band intensity. This was repeated for every possible combination of ONPs to identify the ones present in greatest abundance. Although this provided a clear determination of the optimal answer, the accuracy and precision of the computation were limited by the error inherent in determining DNA abundance via bands in a PAGE gel and by the fact that LCR is an end-point assay. In addition, the procedure required days to complete.

Quantitative real-time PCR (qPCR), which uses an increase in fluorescent signal to monitor increases of PCR amplicons, has proven to be a fast, precise and reproducible method to rapidly quantify the relative abundance of many nucleic acid sequences. This results in part because qPCR is not an end-point assay. Instead, the cycle at which a positive signal is first consistently detectable, termed the cycle threshold (Ct), is proportional to the initial content of a given template in the sample. Higher initial target contents give rise to earlier detectable increases in signal, resulting in lower Ct values. Simultaneous amplifications of multiple DNA targets in a single reaction tube can be achieved by multiplex qPCR, which maximizes throughput and decreases the time required to collect information. Ibrahim et al. [21] reported a qPCR approach to readout answers to a Hamiltonian path problem. However, the protocol required multiple combinations of qPCR amplifications and was ultimately dependent upon the use of in silico information processing to determine the answer.

Answer determination via a direct qPCR amplification of the entire length of TSP answer sequences is impossible. This is due to the intra-molecular heterogeneity of answers sharing the same starting and the ending nodes, which are the same limitations that eliminate the use of DTG-PCR. The application of qPCR for the quantification of the short 20-mer sequences using ONPA for answer determination of a TSP has also not been possible because standard PCR methodologies require two DNA primers that flank the region of the DNA sequence to be amplified. However, we developed a pair ligation probe (PLP)-dependent qPCR system (PLP-qPCR) that is capable of rapidly quantifying the abundance of short DNA sequences under the multiplex conditions [22]. Upon hybridization to its 20-mer target DNA, the PLP becomes circularized by ligation. This allows the abundance of adjacent short sequences in a DNA strand to be transformed into the copy number of circularized PLP that can be amplified by qPCR.

We have now solved an asymmetric, fully-connected 8-city TSP by the ONPA approach using PLP-qPCR without the need for in silico information processing. The validity of using ONPA to derive the optimal answer was confirmed using a reverse-engineering method to reconstruct the complete tours in the feasible answer set from the measured ONPA. The high specificity of the sequence-tagged hybridization and ligation that results from the use of PLPs significantly increased the accuracy of answer determination in DNA computing. When combined with the high throughput efficiency of qPCR, the time required to identify the optimal answer to the TSP was reduced from days to 25 min.

2. Materials and methods

2.1 Oligonucleotide design and construction

Oligonucleotide sequences were designed using Primer Express Version 2 for Windows (Applied Biosystems) and were synthesized by Invitrogen Inc. Nodes labeled B through H were represented by synthetic 20-mer sequences of DNA except for the starting and ending nodes (Astart and Aend) that were comprised of 30-mers (Table 1). Node sequences were chosen to minimize cross hybridization, and nodes B through H had a GC content from 30% to 35% such that melting points varied from 60.6 to 62.0 °C, while the Astart and Aend sequences contained GC contents of 66% and 72%, respectively. None of the arc sequences were complementary to the first 15-mer sequence for the Astart and the last 15-mer sequence for the Aend. Thus, incorporation of Astart or Aend into an answer sequence prevented further extension of that end of the answer sequence. The start and end sequences also served as primer sequences for downstream amplification by PCR, which provided the capability to increase the amount of answer sequences. The longer Astart and Aend sequences with higher GC content were important for downstream PCR amplification with enhanced fidelity and improved efficiency for answer purification. Any two node sequences could be linked together by a 20-mer arc sequence composed of two 10-mers that were complementary to the last and first 10 nucleotides in the sequences of the former and latter nodes, respectively (Figure 1). Arcs were made to complement every combination of nodes with the exception of the respective 5′ and 3′ ends of Astart and Aend. Oligo sequences (Table 2) designed for the PLP-mediated qPCR assay followed the protocol of Xiong and Frasch [23]. All oligonucleotides were purified by PAGE under denaturing conditions [12].

NodeLengthSequence aGC (%)TM (°C)

Table 1.

Node sequences used in the calculation.

All sequences read in the 5′ to 3′ direction.

Blue sequences can hybridize to the 3′-ends of arc sequences.

Green sequences are unable to hybridize to arc sequences but serve as primer sequences for PCR.

Black sequences can hybridize to the 5′-ends of arc sequences.

AS is the sequence for node Astart; the AE is the sequence for the node Aend.

Figure 1.

Graphical representation of the 8-city TSP solved by DNA computing. The optimal tour through the network visits the nodes in alphabetical order. All other tours include arcs that are 100-fold less efficient, and cross at a common point.

DNA sequence
qPCR reporter-identifying sequences
TaqMan-MGB® reporter
Pair ligation arms for node recognition
qPCR primers

Table 2.

Oligonucleotide sequences for the 5′ and 3′ arms of the pair ligation probes, the forward (Pf) and reverse (Pr) primers, and the TaqMan reporters used for PLP-qPCR.

2.2 Answer formation and purification

Hybridization was performed by heating the answer formation reaction medium (AFRM) to 92°C for 4 min, followed by a programmed annealing process at a cooling rate of 1°C per min to 8°C. The AFRM was composed of all relevant oligonucleotides in T4 Ligase Buffer (Fermentas). Ligation was performed by incubating at 8°C for ∼16 h after addition of 5 Weiss U of T4 ligase, 20 mM DTT, and 10 mM ATP to the AFRM.

Ligation products containing all answer sequences were separated by 6% denaturing PAGE containing 8 M urea and 15% formamide at 95 V for about 3 h. The gels were visualized with UV light after staining with ethidium bromide (1 mg/ml) for 10 min. Fragment sizes were determined by comparison with mobility of a 20-bp DNA ladder (Bayou BioLabs). The 190 bp band was excised from the gel that contained sequences consistent in length to those of feasible answers (i.e. containing one copy of each node sequence starting and ending with Astart and Aend). These sequences were amplified by PCR using PCR primers for Astart and Aend, and subject to sequential magnetic affinity purification steps as reported by Spetzler et al. [11, 12] to purify feasible answers.

2.3 Preparation of target-specific pair ligation probes

Each PLP consisted of one 55-mer core and two 10-mer target-specific sequences that comprised the 5′ and 3′ arms located at ends of the core (Table 2). The core sequence contained the forward (Pf 19-mer) and reverse (Pr 21-mer) PCR primer-binding sequences, and a qPCR reporter-identifying sequence known as a TaqMan spacer for use with the TaqMan-MGB® (Applied Biosystems) NED reporter dye (λmax = 580 nm). The PLPs specific for each ONP in the answer sequences were made from core and arm components by ligation as per Xiong and Frasch [23].

2.4 Circularization of the PLP and the qPCR assay

Aliquots of the purified answer sequences containing ∼2 pmol DNA were denatured and annealed with 20 pM of linear PLP. The hybridized PLPs were circularized by ligation at 10°C overnight. The ligation reaction mixture contained 2 μl of 10× ligation buffer (Fermentas), 50 mM DTT, and 5 Weiss U of T4 DNA ligase, in a final volume of 20 μl. After ligation, 2 μl of ligation product was added to 18 μl of the exonuclease mixture that contained 10 mM Tris-HCl, pH 9.0, 5 mM MgCl2, 0.1 mg per ml of BSA, 10 U Exonuclease I and 10 U Exonuclease III to remove any remaining linear PLPs. The samples were incubated at 37°C for 2 h followed by inactivation at 65°C for 20 min.

Quantitative real-time PCR (qPCR) assays were performed in a 96-well, closed plate using the AB 7500 Fast RT-PCR System (Applied Biosystems). In a typical qPCR assay, 20 μl of qPCR reaction mixture that contained 10 μl of 2× TaqMan® Fast universal PCR Master Mix including the ROX fluorescent reporter as a passive reference, 900 nM of each of the Pf and Pr primers, 0.25 μM of the NED TaqMan-MGB® reporter, and ∼2 ng of the circularized PLP were used to determine the abundance of each ordered node pair. Thermal cycling profiles for qPCR included heating at 95°C for 20s followed by 45 cycles with 95°C for 3s and 60°C for 30s.

During the PLP-qPCR assay, DNA amplification was monitored by quantitatively analyzing fluorescence emissions using an ABI prism sequence detector. The intensity of the NED reporter dye was measured against the ROX internal reference dye signal to normalize for non-PCR-related fluorescence fluctuations that occurred from well to well. The threshold cycle (Ct) represented the refraction cycle number at which a positive amplification reaction was measured and was set at 10 times the standard deviation of the mean baseline emission calculated from PCR cycle 5–15.

2.5 Linear programming (LP) model of tour frequency from ONPA data

The model is based on LP approaches to data fitting [24, 25, 26, 27], and solves for the tour frequencies Xt that best fit the observed ONPA Fij .

Subject to:t=15040htijXt+dij+dij=Fijforalli,jE2

where dij+= positive deviation from observed frequency of arc ij; dij= negative deviation from observed frequency of arc ij; Xt = estimated frequency of tour t; htij = 1, if tour t contains ONP ij; 0 otherwise; Fij = observed frequency of arc ij.

The number of possible tours t that begin and end with node A, and visit each node only once is P77= 7! = 5,040. Since the number of DNA molecules of tour t that were made by the DNA computer were not explicitly measured, one Xt variable is generated for each tour t, representing how many DNA molecules of tour t were likely to have been made, given the ONPA. The goal was to solve for the best-fitting values of Xt . Constraints 2 are written once for each ONP ij. The first expression on the left-hand side of the constraint, t=15040htijXt, sums all occurrences of arc ij within all tours t. Constraints 2 then add a positive deviation or error (dij+) and subtract a negative deviation (dij) to the left-hand side and equate it to the observed ONPA Fij . Thus, if there is no set of Xt values that can perfectly reproduce the observed ONPA, the deviation variables are forced to take up any slack or surplus. The objective function 1 minimizes the sum of the deviations so as to find the best-fitting tour frequencies Xt for the observed ONPA Fij . The deviations are separated into positive and negative components because linear programming cannot handle absolute values explicitly. The deviation variables, like the tour frequency variables, are constrained by 3 to be non-negative. If the deviation variables were permitted to be either positive or negative, minimizing their sum would not provide a good fit because the objective would reward large negative deviations pushed toward −∞.

3. Results

The computation to find the optimal solution to an asymmetric, fully-connected 8-city TSP was defined by the distance matrix in Table 3. The problem was designed such that the alphabetical order of the nodes was the optimal tour (Figures 1 and 2d). To accomplish this, the distances were translated into concentrations (1:1 pmol) of the arc sequences that connect the nodes in inverse proportion to the distances (Table 3). These sequences were then hybridized with an excess of all node sequences and ligated to form answer strands as summarized in Figure 2. Node and arc sequences were asymmetric in design so that two node sequences could become ligated in an order-specific manner to form an ordered node pair (ONP). For example, to compute the formation of the BC-ONP, the last (3′) and first (5′) halves of the sequences for nodes B and C hybridize to the first (3′) and last (5′) halves of the BC arc oligonucleotide, respectively, which then permits ligase to link them covalently.

PriorSubsequent node
AS* a (0) b1 c (100) b100 (1)100 (1)100 (1)100 (1)100 (1)100 (1)100 (1)
B* (0)* (0)1 (100)100 (1)100 (1)100 (1)100 (1)100 (1)100 (1)
C* (0)100 (1)* (0)1 (100)100 (1)100 (1)100 (1)100 (1)100 (1)
D* (0)100 (1)100 (1)* (0)1 (100)100 (1)100 (1)100 (1)100 (1)
E* (0)100 (1)100 (1)100 (1)* (0)1 (100)100 (1)100 (1)100 (1)
F* (0)100 (1)100 (1)100 (1)100 (1)* (0)1 (100)100 (1)100 (1)
G* (0)100 (1)100 (1)100 (1)100 (1)100 (1)* (0)1 (100)100 (1)
H* (0)100 (1)100 (1)100 (1)100 (1)100 (1)100 (1)* (0)1 (100)
AE* (0)* (0)* (0)* (0)* (0)* (0)* (0)* (0)* (0)

Table 3.

Arc distance and corresponding concentration matrices used to make the computation.

Arc does not exist.

pmoles of arc molecules input into a final volume of 56 μl are shown in parentheses.


Figure 2.

Protocol used to compute the 8-city TSP. Answers were formed by the addition of saturating amounts of all nodes and limiting amounts of arcs in inverse proportion to their respective distance. Upon hybridization, nodes and arcs were ligated to form answers. The ligation was accomplished in two stages to increase the probability of forming feasible answers that contained a single copy of each node flanked by the start and end sequences. Infeasible answers were removed by PAGE and by magnetic affinity purification as described in Section 2. Examples of infeasible answer sequences formed include those that are: (a) too short because they lack one or more nodes; (b) too long because they contain multiple copies of nodes; and (c) the correct length but lack at least one node. Feasible answers were subjected to PLP-qPCR for ONPA. Examples of feasible sequences include: (d) the optimal answer sequence with the nodes in alphabetical order; (e) a suboptimal sequence that contains a minimum substitution of 3 arcs from the optimal (see Table 5, normalized data row 2), and (f) an even less optimal sequence in which 4 arcs have been substituted from those found in the optimal answer (see Table 5, normalized data row 3).

Given that the concentration of arcs along the upper diagonal of the efficiency matrix was 100-fold that of the other arcs, strands containing node sequences in alphabetical order were anticipated to be produced in highest abundance. A comparable result was obtained previously using a similar approach to solve an asymmetric, fully-connected 15-city TSP [10]. Consequently, this computational method could be reliably used to examine the efficacy of PLP-qPCR in the answer determination step of a DNA computation.

A tour of the nodes was feasible, whether it was optimal or suboptimal, only if it contained one copy of each node sequence flanked by the Astart and Aend sequences (Figure 2d–f). Figure 3 shows a stepwise summary of the procedure used to make the calculation. The PAGE profile of answer sequences at various stages of purification is shown in Figure 4. Selective amplification of answer sequences flanked by Astart and Aend (Lane 1) was achieved by PCR using primers specific for those sequences (Figure 2a–f). This PCR product (Lane 2) included the 190-mer band that was the size required for feasible answers (Figure 2c–f), which was then subjected to sequential magnetic bead affinity purification for every node sequence. This insured that all sequences used for answer analysis contained one and only one copy of each node sequence, and thus represented Hamiltonian circuits through the network. The purified sample composed only of answer DNA sequences for feasible tours (i.e. Figure 2d–f) appeared as a single 190-mer band (Lane 3) that was used to determine the optimal answer to the computation.

Figure 3.

Graphical representation of the process to make, and purify DNA sequences that represent correct answers, and the use of PLP sequences for ordered node pair analysis to identify the optimal tour. Details of the methods are described in Section 2.

Figure 4.

Profiles of DNA computing products by super denaturing PAGE following amplification by PCR using primers specific to AS and AE. 1: Initial product of hybridization/ligation from the answer formation process. Black arrow indicates the 190-mer band that was excised for subsequent purification. 2: Purified 190-mer band excised from Lane 1. 3: Feasible answer sequences following sequential magnetic affinity purification to insure the presence of every node sequence. M: Molecular size reference using a 20-mer DNA ladder where the 100-mer was the brightest band (red arrow).

To identify the optimal answer, the feasible answers (Figure 4, Lane 3) were analyzed by the ONPA approach. This was accomplished using PLP-qPCR with the 56 PLPs that were specific to each of the possible ONPs. Each PLP was added to an aliquot of the solution containing the answer set to prepare it for PLP-qPCR. Preparation included the steps summarized in Figure 5 for the BC-PLP that was used to detect the ONP in which the sequence encoding node B immediately precedes that of node C in a tour. For the BC-ONP, the 5′-arm of the PLP complementary to the last 10 bases of sequence B (designated B′), and the 3′-arm (designated C″) that were complementary to the first 10 bases of sequence C were created [23]. The hybridized PLP was circularized by ligase, after which the PLP was denatured from the target strand and exonuclease was added to eliminate any DNA that had not been circularized. Because the amount of circulated PLP was quantitatively related to the initial content of a target, the target content used in the determination was transformed into the copy number of the circularized PLPs. The presence of a qPCR reporter-identification sequence, and PCR primers in the PLP enabled the use of qPCR to measure the copy number.

Figure 5.

Use of pair ligation probes (PLPs) to quantify the abundance of the nucleotide sequence encoding the BC ordered node pair (BC-ONP) where node B precedes node C. (1) The PLP hybridizes to 20 consecutive bases of the BC target sequence. (2) T4 ligase circularizes the hybridized PLP. (3) Circularized PLP is denatured from target, and Exonuclease I eliminated any nucleic acid not circularized. (4) qPCR quantifies PLP abundance upon addition of the TaqMan-MGB® reporter, PCR primers and nucleotides.

Figure 6 shows the PLP-qPCR fluorescence amplification plots as a function of cycle number that determines the amount of each possible ONP in the answer sequences of the 8-city TSP. The ONPA was determined in groups according to the prior node in the ONP such that the relative abundance of any of the ONPs in that group could be compared directly. In each case, it is evident that the first sample in which fluorescence amplification consistently increased above the threshold corresponded to that ONP where the nodes appeared in alphabetical order (i.e. AB, BC, etc.). Thus, it was possible to determine the optimal answer to the 8-city TSP using PLP-qPCR by simple inspection of the raw data. Due to the quantitative nature of qPCR, the Ct values measured from the data in Figure 3 were used to calculate the copy number of each ONP (Table 4). The results are organized so that each row and column define the prior and subsequent nodes of each ONP. Since these measurements were made in groups corresponding to each row, comparisons of the ONPA between rows were achieved by determining the fractional ONPA after normalizing the ONPA present in each row in highest abundance (data in parentheses). The average copy number for suboptimal ONPs was 0.35% of the optimal ONP in each row. However, the suboptimal ONPs were not present in equal abundance. Seven of the suboptimal ONPs were present in amounts that were below the limit of detection. However, the ability to detect these low abundance ONPs was not needed to obtain the optimal answer to the problem solved here. Some of the suboptimal ONPs were formed in much higher abundance than the average. Figure 7A shows the number of suboptimal ONPs from Table 4 as a percentage of the preceding node in the pair. The fraction of suboptimal ONPs was significantly larger in rows C, D, E and F in Table 4. This was due to a relatively small number of specific alternate ONPs that included CE (0.2%), DA (0.2%), EC (0.47%), FD (0.5%), and FE (0.47%).

Figure 6.

Abundance of ONPs in the feasible answer sequences determined by PLP-qPCR. A separate PLP was designed to detect the amount of each of the 56 possible ONPs (ASB, ASC, etc.). Each PLP contained a qPCR reporter identification sequence for use in fluorescence detection with the TaqMan-MGB® reporter for NED. Plots of fluorescence intensity as a function of PCR cycle number are grouped by the preceding node in the ONP. Each of these groups was run as single-plex assays on a 96-well plate using aliquots from a common solution of answer sequences so that the assays within each group are comparable. The latter node in the ONP is indicated as B (●), C (■), D (○), E (▽), F (▲), G (△), H (□), and AE (▼).

Prior nodeSubsequent node
AS1.4 × 106 a103.52.90.0190.191.4*
B*4.8 × 1050.4961094.921
C0.04*2.2 × 1054200.186.4220
D28.5190*3.5 × 10539532048.5750
E6401600380*3.4 × 105871.50
F1.5018001600*3.4 × 105380380
G0.870.0570470*1.2 × 10531
H0.4221.60470.34*7.9 × 106

Table 4.

ONPA in the set of feasible answers from the 8-city TSP determined by PLP-qPCR.

All values are in 1000s of molecules.

Figure 7.

(A) Dominant suboptimal ONPs present in the answer sequences. The subsequent node in the ONP is indicated in each bar, and the sum of all other suboptimal ONPs in a given row from Table 5 is indicated in yellow. (B) Combined probability of tours reverse engineered by the LP Model as a function of the Number of Suboptimal ONPs. The combined probability is the sum of the probabilities of all tours containing a given number of suboptimal ONPs generated from the normalized (●) and absolute data (□ of Table 5). The optimal tour did not contain suboptimal ONPs. From 1 to 9 tours were reverse engineered for each number of suboptimal ONPs shown.

To test the validity of using ONPA to identify the optimal answer of a TSP, a linear programming (LP) model containing 5168 variables and 64 constraints was developed to “reverse engineer” the frequency of the feasible tours formed by DNA computing that would most closely match the individual ONP frequencies found in Table 4 when broken down into their constituent ONPs. Since the data for each row in Table 4 were obtained independently from the others, the model 1–3 was solved by inputting either the normalized and absolute ONP frequencies in Table 4 as the Fij parameters. In the normalized model, the Fij were converted into percentages of each row total, whereas in the absolute model, the Fij values were the total number of molecules detected (see Table 5 footnotes a and b).

Normalized ONPA Fij aAbsolute ONPA Fij b
Top five tours c# suboptimal ONPsProbabilityTop five tours d# suboptimal ONPsMolecules (in 1000s)Probability

Table 5.

Tour probabilities reverse engineered from observed ONPA by the LP model.

Based on ONPA as a percent of total molecules in each row in Table 4 (i.e. ΣFij on Row As = 1.00, ΣFij on Row B = 1.00, etc.).

Based on ONPA in Table 5 (i.e. ΣFij on Row As = 1.5 e9, ΣFij on Row B = 4.5 e8, etc.).

A total of 30 non-zero tours were reversed engineered from Normalized data with 0.0299702 total absolute deviations (objective function value).

A total of 32 non-zero tours were reverse engineered from Absolute data with 9,057,230,000 total absolute deviations (objective function value).

For the normalized model, the largest individual deviation is for the FG-ONP. The observed abundance FFG was 0.98791. In the optimal solution, summed over all reverse-engineered tours (t=15040htFGXt), arc FG was part of 0.99215 of the tours formed. Therefore, the FG-ONP would have a negative deviation dFG= 0.00425 and a positive deviation dFG+= 0. Many sets of positive and negative deviations exist that could equalize this constraint. However, the set that contributes the smallest amount to the objective results from the case in which one or both of the positive and negative deviations are zero, because the objective function adds both positive and negative deviations. In addition, there exist many possible solutions with Xt values such that t=15040htFGXt= FFG = 0.98791 exactly, but none of them were optimal because it would have increased the deviations for other ONPs. The same set of Xt values appeared in all 64 constraints and, while there is no set of Xt values that can satisfy all 64 instances of constraint 2 perfectly with no deviations, the model was designed to minimize the sum of the deviations for all ONPs simultaneously.

When the normalized ONPA data from Table 4 were input, 99.01% of feasible tours formed by the DNA computer are estimated to have been the optimal tour ABCDEFGHA. Given the relative proportions of the ONPs formed, no other tour is likely to have comprised more than 0.38% of the tours formed (Table 5), which was the percentage for the second-most frequently formed tour in the reverse-engineering model (ASBFECDGHAE). Of the 5040 possible tours in the LP model, the optimal reverse-engineered set of tours had only 30 tours with a non-zero frequency. The objective function value in the model of the normalized data (the sum of the positive and negative deviations over all 64 ordered node pairs) was 0.02997.

Using the absolute molecule frequencies as the Fij values, the LP model estimated that 339,742 molecules, or 99.13% of all feasible tour molecules, were the optimal answer. The next most frequently produced tour by the DNA computer was estimated to have formed only 1259 molecules (Table 5). As expected, the error levels increased dramatically when the model was used to reverse-engineer the tours formed from the absolute molecule frequency. This occurred because the row sums of molecules in Table 4 were determined in separate qPCR measurements without controlling for the absolute amount of answer sequences used in the samples between rows. Had this been held constant during the measurement, the total number of molecules in each row of Table 4 should be the same because each feasible answer contains one copy of each node sequence. The total deviations summed to 9,057,230, which represents 81.57% of the total Σ i Σ j Fij , compared with only 0.37% for the normalized model. It is noteworthy that, in the model based on the absolute data, the five ONPs with the greatest deviations from the observed frequencies (HAE, ASB, GH, BC, CD) were all part of the optimal tour, whereas only two such ONPs were among the top five deviations (FG, BF, DG, BC, and FD) when matching to the normalized ONPA. Despite the fact that the deviations derived from the absolute ONPs were much higher, the DNA computation still returned the optimal tour over 99% of the time.

A fully connected 8-city TSP was solved by the ordered node pair abundance (ONPA) approach through the use of a pair ligation probe quantitative real time polymerase chain reaction (PLP-qPCR) system. The high specificity of the sequence-tagged hybridization and ligation that results from the use of PLPs significantly increased the accuracy of answer determination in DNA computing. When combined with the high throughput efficiency of qPCR, the time required to identify the optimal answer to the TSP was reduced from days to 25 min.

The reverse-engineering LP model provides additional evidence that the DNA computer can distinguish the quality of solutions to the TSP. Although the problem was set up artificially to have a single solution that was far better than any other possible solution, the reverse-engineering LP model confirms that the optimal solution was produced in far greater abundance than any other answer, and among the suboptimal solutions, those with greater optimality were generally produced in greater abundance than those that were less optimal.

Examination of the less frequently produced tours provides a measure of the sensitivity of DNA computer to the abundance of the arc sequence molecules initially input to carry out the computation. To make any change to the optimal tour ASBCDEFGHAE, at least three ONPs in the tour must be different. For example, the tour with penultimate optimality (Figure 2e) must have 3 ONPs that are different from the optimal (Figure 2d), while tours containing 4 different predominant ONPs (Figure 2f) would be even less optimal, and so forth. As shown in Table 5, among the 2nd-5th most frequently produced tours for models predicted from both the absolute and normalized data, all but one exhibit either three or four ONP changes from the optimal tour. When the probabilities of the tours were summed over all tours with a given number of suboptimal ONPs, the frequency of tours formed with more suboptimal ONPs exponentially declined as a function of an increase in the number of suboptimal ONPs incorporated (Figure 7B). Thus, not only did the DNA computer generate the optimal answer far more frequently, but other answers were generated in amounts that were inversely proportional to their objective function value.

Even though the data of Table 4 were obtained in separate sets grouped according to each row without controlling for the abundance of molecules between rows (absolute data), the computation returned the correct answer, demonstrating the robustness of this approach. Several ONPs were not detected as products of the computation (e.g. FB). However, this does not imply that no molecules of these ONPs were formed. Although the amounts of these ONPs were below the level of detection, this did not alter the determination of the optimal answer to this problem because the efficiency of the tour that gave rise to the optimal answer was so much greater than any other tour. Identification of the optimal answers to some less obvious problems may require a more sensitive discrimination of ONPA. Under these circumstances, to quantify smaller amounts of ONPs or to discriminate between smaller differences in abundance of two specific ONPs, the PLP-qPCR can be repeated using larger aliquots of feasible answer solutions.


This work was supported by grants to WDF from DARPA-DSO and AFOSR (FA95500710219). The Fair Isaac Corp. ( provided the Xpress Optimization Suite to the university under their Academic Partnership Program.

© 2020 The Author(s). Licensee IntechOpen. This chapter is distributed under the terms of the Creative Commons Attribution 3.0 License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Fusheng Xiong, Michael Kuby and Wayne D. Frasch (March 19th 2020). Accelerating DNA Computing via PLP-qPCR Answer Read out to Solve Traveling Salesman Problems, Novel Trends in the Traveling Salesman Problem, Donald Davendra and Magdalena Bialic-Davendra, IntechOpen, DOI: 10.5772/intechopen.91663. Available from:

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