Inference of chromosome-specific copy numbers using population haplotypes
- Yao-Ting Huang^{1}Email author and
- Min-Han Wu^{1}
DOI: 10.1186/1471-2105-12-194
© Huang and Wu; licensee BioMed Central Ltd. 2011
Received: 31 October 2010
Accepted: 24 May 2011
Published: 24 May 2011
Abstract
Background
Using microarray and sequencing platforms, a large number of copy number variations (CNVs) have been identified in humans. In practice, because our human genome is a diploid, these platforms are limited to or more accurate for detecting total copy numbers rather than chromosome-specific copy numbers at each of the two homologous chromosomes. Nevertheless, the analysis of linkage disequilibrium (LD) between CNVs and SNPs indicates that distinct copy numbers often sit on their own background haplotypes.
Results
We propose new computational models for inferring chromosome-specific copy numbers by distinguishing background haplotypes of each copy number. The formulated problems are shown to be NP-hard and approximation/heuristic algorithms are developed. Simulation indicates that our method is accurate and outperforms the existing approach. By testing the program in 60 parent-offspring trios, the inferred chromosome-specific copy numbers are highly consistent with the law of Mendelian inheritance. The distributions of copy numbers at chromosomal level are provided for 270 individuals in three HapMap panels.
Conclusions
The estimation of chromosome-specific copy numbers using microarray or sequencing platforms was often confounded by a number of factors. This study showed that the integration of background haplotypes is able to improve the accuracies of copy number estimation at chromosome level, especially for the CNVs having strong LD with SNPs in proximity.
Background
Genetic variations exist in many forms in the human genome. Large structural variations such as deletions and duplications are quite common in the human populations, which encompass more base pairs than single nucleotide polymorphisms (SNPs). Among various types of structural variations, copy number variations (CNVs) often occupy regulatory regions of genes and greatly influence phenotypic traits and disease susceptibility [1]. CNV is defined as a DNA segment with length more than 1 kb and observed with various numbers of copies in the population. A number of CNVs have been known to highly associate with several complex diseases such as HIV infection, autoimmunity, autism, Parkinson's, Alzheimer's and Crohn's disease [2–6].
The advance of high-throughput array platforms and sequencing technologies enables fast and cost-effective scan of CNVs in genome-wide scale [7]. Using array Comparative Genomic Hybridization (aCGH) and next-generation sequencing, a large number of CNVs have been identified in human and other primates [8–12]. In practice, because our human genome is a diploid, most sequencing platforms often report total copy numbers of one individual instead of chromosome-specific copy numbers presented on each of the two homologous chromosomes. For example, suppose there are two diplotype configurations at one CNV locus: 1/1 represents one copy at each of the two chromosomes, and 0/2 indicates a deletion at one chromosome and a duplication at the other. The total copy numbers of these configurations are both experimentally obtained as two, although the underlying mechanisms generating these two configurations are different. Nevertheless, determination of chromosome-specific copy numbers is important in the analysis of population genetics and disease association studies. For instance, the power of detecting positive selection and accuracy of measuring Linkage Disequilibrium (LD) between SNPs and CNVs can be improved through direct use of chromosome-specific copy numbers [13–15]. Moreover, identification of the chromosome-specific copy numbers can even shed light on the age of each CNV [1].
Recently, an expectation maximization (EM) algorithm was developed to estimate frequencies of chromosome-specific copy numbers under the assumption of Hardy-Weinberg equilibrium (HWE) [16]. In reality, the observed allele frequencies do not completely satisfy HWE, because each copy number allele may be sampled more or less in different sequencing projects. In a few occasions, HWE may be even deviated due to directional selection, assortative mating, or migration [17]. Using B allele frequencies (BAF) and log R ratios (LLR) provided by SNP array platforms, a hidden Markov model (HMM) was designed for inferring chromosome-specific copy numbers within a parent-offspring family [18]. In addition, information of allelic-specific copies at each SNP locus (e.g., AAABB) have been also used to indirectly infer chromosome-specific copy numbers [19]. However, BAF, LLR and allelic-specific copies are not always available in each sequencing platform. For example, in next-generation sequencing (e.g., SOLid and Illumina), SNPs and CNVs called at these platforms (e.g., Bioscope and SAMTools) do not provide such information. Moreover, the accuracy of allelic-specific copies is often decreased for higher copies and is worse than that of total copy numbers due to cross-hybridization [20, 21]. Although traditional haplotype phasing programs (e.g., fastPHASE) may be used for inferring copy number by encoding bi-allelic CNVs into SNP genotypes, this approach is inadequate to infer multi-allelic CNVs [13, 19].
To date, the analysis of LD structure in human genome indicated that many CNVs have strong LD with SNPs in proximity, probably owing to uneven distribution of recombination hot/cold spots or genetic hitchhiking [22–25]. Moreover, a number of CNVs have been shown to be taggable using alleles at flanking SNPs [3]. The LD structure between CNVs and SNPs implies different chromosome-specific copy numbers often sit at their own background haplotypes, which can be viewed as fingerprints of each copy number. As a consequence, chromosome-specific copy numbers of each individual are inferable by careful analysis of background haplotypes around each CNV. In recent years, several large-scale sequencing projects have constructed complete haplotype and CNV databases across major human populations (e.g., HapMap [26]). Integration of these databases may gain insight into the distribution of chromosome-specific copy numbers in human populations.
In this study, we develop new computational models and combinatorial algorithms for inferring chromosome-specific copy numbers by distinguishing background haplotypes of each copy number. Two optimization problems are formulated, shown to be NP-hard, and solved by approximation or heuristic algorithms. Simulation indicates our method is very accurate and is able to outperform existing approach. By testing the program separately for each individual within 60 parent-offspring trios, the inferred chromosome-specific copy numbers are highly consistent with the law of Mendelian inheritance. The distribution of chromosome-specific copy numbers across three human populations indicate that one copy is the major allele as expected, and zero copy (deletion) alleles are much frequent than high copy (duplication) alleles.
Methods
The haplotypes of 270 individuals are downloaded from the Phase II of international HapMap project [26]. For the input of unphased genotypes, the haplotypes were inferred via the PHASE [27] program, which was used by the HapMap project. For high-throughput sequencing data, a number of haplotype assembly tools can also be used to infer the haplotypes [28]. The total copy numbers of 1,319 CNVs typing on the same individuals are retrieved from [9]. We extract SNPs within each CNV as well as SNPs at flanking regions in our study. We compared the SNP distance (i.e. number of SNPs) with the physical distance (e.g., 5 kb) for capturing the extent of LD and found that the LD is more sensitive to physical distance. The simulation results indicated that the accuracy of our algorithm is highest when including SNPs within one-fold extension of the physical size of each CNV (Additional file 1, Figure S1). Therefore, the released program will automatically checks the coordinates of CNVs and SNPs and captures SNPs within the one-fold extension regions into consideration.
Haplotypes Clustering via Solving Constrained Max-k-Cut Problem
- (1)
Each haplotype is transformed into a vertex.
- (2)
The weight of edge between two vertices is the hamming distance between two haplotypes. Note that the same haplotype from different individuals are formulated as multiple vertices with zero distance.
- (3)
For the haplotype pair with odd total copy number (e.g., H _{1} and H _{2}), the edge between them is called hard edge.
- (4)
For the other haplotype pairs, the edges between them are called soft edges.
Given the above weighted graph with hard and soft edges, these haplotypes are grouped into k clusters by solving a variant of Max-k-Cut problem (called constrained Max-k-Cut). A formal definition of the constrained Max-k-Cut problem is given below.
Problem: Constrained Max-k-Cut
Given an undirected weighted graph G = (V, E) in which some edges in E are hard and the others are soft, the constrained Max-k-Cut problem aims to find a partition of vertices in V into k sets (X_{1}, X_{2}, ..., X_{ k } ) such that the total weight of soft edges across different sets (called cut) is maximized, requiring all hard edges must be on the cut.
The original Max-k-Cut is known to be NP-hard [29, 30], which is a special case of this problem when all edges are soft. Therefore, the problem of constrained Max-k-Cut is also NP-hard. In order to efficiently solve the constrained Max-k-Cut problem, we develop a greedy approximation algorithm which explores larger solution space by randomizing non-deterministic steps. The core procedure of this algorithm is given below (Additional file 2, Figure S2).
Algorithm for Constrained Max-k-Cut
- (1)
Randomly pick k different vertices as initial elements for each k set (X _{1}, X _{2}, ..., X_{ k } ).
- (2)
Without violating the constraint of hard edge, randomly pick a remaining vertex and assign it into the set which maximizes the total weight of soft edges across different sets. This step is repeated until all vertices are assigned.
Note that the above procedure involves non-deterministic parts in both steps (i.e., initial k vertices and the order of picking the next vertex). Therefore, this procedure is repeated ten times to explore larger solution space by trying different initial k vertices in step 1 and different order in step 2. The best solution among all trials is outputted as the final solution. The number of repeated iterations is usually a tradeoff between accuracy and efficiency. Nevertheless, we found that the randomized approaches on top of the greedy framework requires only few iterations (Additional file 3, Figure S3). Thus, the implemented can run fast in practice. The following theorem implies that the solution found by this algorithm is quite close to the optimal solution.
Theorem 1. The algorithm for constrained Max-k-Cut is a (k - 2)/(k - 1)-approximation algorithm for k > 2.
Copy Number Assignment via Solving Constraint Satisfaction Problem
where X_{ a } and X_{ b } denote the sets of these two haplotypes after clustering (e.g., X_{1} + X_{3} = 2 for individual 3). For each individual, a set of constraints with two variables similar to eq (2) can be generated by repeating the above formulation (see Figure 3(B)). By assigning distinct integer numbers to these set variables X_{ i } , chromosome-specific copy number of each haplotype can then be determined. Theoretically, all constraints should be satisfied after the assignment, but practically, not all constraints can be satisfied, because some ambiguous haplotypes may not be the true background of the copy number. In order to satisfy as many constraints as possible, chromosome-specific copy numbers are assigned to each set X_{ i } by solving a variant of the constraint satisfaction problem (termed Unique Max-2-CSP). Given a set of two-variable constraints over n variables (X_{1}, X_{2},..., X_{ n } ), the Unique Max-2-CSP problem asks for k unique (distinct) integers assigned to each variable which satisfied maximum number of constraints.
Problem: Unique Max-2-CSP
where T_{ l } is a non-negative integer. The Unique Max-2-CSP asks for an assignment of n distinct integers in D to X_{1}, X_{2}, ..., X_{ n } that maximizes the total number of satisfied constraints in C.
We first prove a problem called binary Max-2-CSP is NP-hard, in which the integer domain D is restricted to {0, 1}, and values assigned to different variables in X are allowed to be identical (e.g., X_{1}= X_{2}= 1).
Then, the unique Max-2-CSP problem is shown to be NP-hard by reduction from binary Max-2-CSP. The details of these proofs can be found in Additional file 4, Supplementary Material.
Theorem 2. Unique Max-2-CSP is NP-hard.
In order to solve unique Max-2-CSP more efficiently, we developed a greedy heuristic algorithm which also explores larger solution space by randomizing non-deterministic steps. Let n be the number of individuals and c_{ max } be the maximum possible copy number.
Algorithm for Unique Max-2-CSP
- (1)
Initially set X_{ i } = c.
- (2)
Randomly pick a constraint {N : X_{ a } + X_{ b } = T } in which only X_{ a } (or X_{ b } ) is assigned, where N is the number of the constraint. If X_{ a } (or X_{ b } ) = D, and there are m types of constraints with X_{ a } + X_{ b } as following: {N_{ j } : X_{ a } + X_{ b } = T_{ j } }, where 1 ≤ j ≤ m, and N _{1} is maximum in N_{ j } , assign X_{ b } (or X_{ a } ) = T _{1} - D. Repeat this step until there is no constraint in which only one variable is assigned.
- (3)
Compute the number of satisfied constraints with respect to X_{ i } = c.
Ideally, once the value of the initial variable X_{ i } is assigned (e.g., X_{1} = 0), the values of other associated variables can be indirectly determined (e.g., X_{1} + X_{2} = 1 or X_{1} + X_{3} = 2). However, there could be some conflicting constraints existed (e.g., X_{2} + X_{3} = 3). Therefore, the possible values of all variables X_{ i } are dependent on the order of assignment (e.g., X_{1} = 0 first, X_{2} = 1 second, then ...). In reality, there are more variables and the dependency/conflict relations are more complicated. Consequently, we repeat the above procedure ten times to explore different orders of assignments by randomly prioritizing distinct constraints to be satisfied in different rounds. The best solution among all iterations is recorded into the corresponding row in the solution table. Note that some variables may have no assignment due to conflicts with previously assigned variables and hence are recorded as -1.
- (4)
Select a row which is not chosen in the solution table with maximum number of satisfied constraints. Repeat this row selection until no further constraints can be satisfied. Note that the variables assigned in one iteration cannot violate the assignment in previous iteration.
Finally, the union of assignments selected by this greedy algorithm is outputted as the solution.
Iteration and Adjustment
- (1)
Randomly pick an individual with haplotypes violating the constraint and enumerate all possible assignments for these two haplotypes such that the constraint can be satisfied.
- (2)
For each possible assignment, evaluate the new cut value in the Max-k-Cut problem and choose the assignment with maximum cut among all possibilities.
- (4)
Repeat step (1) and step (2) for the remaining unsatisfied individuals until all of them are satisfied.
Because the order of individuals processed is non-deterministic, we also repeat above procedure ten times and output the best solution among them.
Simulation
The simulation of LD and HWE generated two series of copy numbers and SNP genotypes from 16 individuals. The haplotype phases are inferred via PHASE [27]. The first series of data sets simulate diplotype configurations completely match HWE (P = 1.0, Chi-square). The flanking SNPs are simulated starting from perfect LD (average r^{2} = 1.0). Subsequently, the remaining data sets of lower LD are constructed by flipping SNP alleles at random. The second set of experiments simulated an imperfect HWE data sets by adding/deleting some copy number alleles from the HWE data sets, which aims to slightly deviate from the expected HWE frequency (P = 0.98). The remaining data sets of LD decay are generated in a similar way.
The simulation using copy number on X Chromosomes is also adopted. Because there is only one X chromosome in each male, the total copy number obtained on X chromosome directly represents the chromosome-specific copy number [9]. We use CNVs and haplotypes in X chromosomes of males from the HapMap project during simulation. The total copy numbers at one CNV is simulated by randomly pairing two copy numbers on two different X chromosomes.
where C_{ correct } is the number of correctly inferred copy number configurations and C_{ total } is the total number of configurations.
Results
The proposed algorithms have been implemented as a program called CSCNPhaser, which is available at http://www.cs.ccu.edu.tw/~ythuang/Tool/CSCNPhaser/. We retrieved haplotypes of 270 individuals from Phase II of the International HapMap Project [26]. These individuals include 30 trios from the Utah, USA region (CEU); 30 trios from the Yoruba in Ibadan, Nigeria (YRI); 45 unrelated Japanese individuals from Tokyo, Japan (JPT); and 45 unrelated Han Chinese individuals from Beijing, China (CHB). In addition, total copy numbers at 1,319 CNVs typing on the same 270 individuals are downloaded from [9]. We consider haplotypes within the CNV as well as haplotypes at flanking regions, whereas the best length of extended haplotypes is determined by simulation (see Method).
Simulation on LD Decay and HWE
The second set of experiments simulated an imperfect HWE data sets by adding/deleting a few copy number alleles to slightly deviate from the expected HWE frequency (P = 0.98). Note that the entire allele frequency spectrum is still close to that of HWE. Figure 6(B) plots the accuracies of CSCNPhaser and CNVPhaser at different degrees of LD. In high LD, both programs can still achieve high accuracies.
Although the major trends are similar to previous experiments, CNVPhaser is slightly worse than previous experiment compared with our method, implying it is more sensitive to HWE deviation.
Consistency with Mendelian Inheritance
Distributions of Copy Number Configurations in Human Populations
On the other hand, 0/1 and 0/0 configurations (hemizygous and homozygous deletions) are more frequent than the remaining duplication forms, probably due to the low frequencies of high-copy alleles. Although these distributions are consistent across three HapMap panels, these results could be still biased due to low-LD background of recurrent or translocation-mediated CNVs. Therefore, these distributions are for reference only, which require experimental validations before further interpretation.
Capability and Efficiency
Discussion
Strength and Weakness of LD-based Inference
CNVPhaser was developed by estimating allele frequencies using HWE, while our CSCNPhaser investigated the haplotype background of each copy number. Although not explicitly stated, we observed CNVPhaser implicitly capture background haplotypes in a light way, because the frequencies are estimated over the entire copy number/haplotype combinations. Therefore, its accuracy also decreases as LD decays. For CNVs having high LD with flanking SNPs, our program performs better than CNVPhaser. In low LD regions with only 1/1 configurations, we observed that CSCNPhaser may miscall them as 0/2 configurations. On the other hand, in data sets with mixed configurations (i.e., 1/1 and 0/2), we observed that the miscalled rate is lower, because these data sets contain haplotypes LD-informative of 0/2 configuration, which are used for better distinguishing 1/1 from 0/2 configurations in our algorithm. Most common, diallelic CNVs have been found to have strong LD with flanking SNPs, and most low-frequency CNVs even segregated on specific haplotype background [9]. Therefore, we anticipate it is useful to look at the haplotype background for inferring copy number of most CNVs.
Accuracies on X chromosome Simulation.
CNV IDs | Exp. 1 | Exp. 2 | Exp. 3 | Exp. 4 | Exp. 5 |
---|---|---|---|---|---|
16 CNVs | 0.788272 | 0.828395 | 0.869445 | 0.917284 | 0.953704 |
CNV2621 | 0.585185 | 0.618519 | 0.611111 | 0.666667 | 0.685185 |
CNV2682 | 0.314815 | 0.222222 | 0.359259 | 0.292593 | 0.285185 |
Copy numbers of the 18 CNVs on X chromosomes.
CNVid | Copy Number | CNVid | Copy Number |
---|---|---|---|
2593 | 0,1 | 2654 | 0,1 |
2603 | 0,1 | 2659 | 0,1 |
2604 | 0,1 | 2675 | 0,1 |
2619 | 0,1 | 2678 | 0,1 |
2621 | 0,1,2 | 2682 | 1,2,3 |
2627 | 0,1 | 2694 | 0,1 |
2636 | 1,2 | 2704 | 0,1 |
2639 | 1,2 | 2706 | 0,1 |
2648 | 0,1 | 2707 | 1,2 |
Strategies for Solving Constrained Max-k-Cut
The original Max-k-Cut problem can be solved by a randomized algorithm which randomly partition all vertices into k sets. In addition, it can be also solved by a deterministic greedy algorithm which iteratively assigns one vertex into the set that maximizes the cut size. In fact, both algorithms return a good approximate solution within a factor of of the optimal solution, and the semidefinite-programming (SDP) relaxation can achieve a better approximation bound [30]. Therefore, it is natural to consider the three strategies for solving the constrained version. Although not presented in this paper, the random partition method was ever considered but later withdrawn due to the bad accuracies in all experiments. It is because the random partition method simply guess the solution, which can't work in practice although the approximation ratio is theoretically good. The SDP strategy is theoretically sound but the running time is slow in our previous study [33], and the SDP implementation is complex so that the program is often not easily portable to all platforms. On the other hand, the greedy algorithm (with randomization enhancement) can achieve high accuracies and run very fast in all experiments. As a consequence, the greedy solution is taken in order to perform genome-wide experiments with high accuracies and within reasonable period of time.
Integration of Greedy and Randomized Approaches
Theoretically, the two optimization problems (Max-k-Cut and Max-2-CSP) can be both solved by a deterministic greedy approach or a pure randomized approach (e.g., random partition for the k-cut problem). The greedy approach is simple and fast. However, the solution found is often only theoretically sound but not comparable with other heuristic methods in practice. This is due to the fact that the ordinary greedy approach tends to find local optimum solution instead of global optimum solution. On the other hand, the pure randomized (blind-search) approaches do not have the tendency of finding local optimum solution but requires numerous iterations for finding a good solution. Therefore, when solving both algorithms, we used the greedy algorithm as a framework and randomized the non-deterministic steps for searching better solutions. The results showed that the iterations required of this hybrid approach are far less than those of pure randomized approaches, while obtaining better solutions than an ordinary greedy algorithm.
Conclusion
In this study, we developed new computational models and combinatorial algorithms for inferring chromosome-specific copy numbers by distinguishing their haplotype background. Simulation showed that our method is accurate and outperformed existing method as the background haplotypes are LD-informative of the copy numbers. The inferred copy numbers are consistent with Mendelian inheritance for 97% of CNVs within parent-offspring trios. The inference of copy numbers in microarray and sequencing platforms are often confounded by a number of different factors. This study showed that integration of haplotypes into copy number estimation is able to improve the accuracies, especially for those CNVs having strong LD with SNPs.
Declarations
Acknowledgements
We thank the reviewers for their valuable comments. Yao-Ting Huang and Min-Han Wu were supported in part by NSC grant 98-2621-B-194-001 from the National Science Council, Taiwan.
Authors’ Affiliations
References
- Kato M, Nakamura Y, Tsunoda T: An algorithm for inferring complex haplotypes in a region of copy-number variation. The American Journal of Human Genetics 2008, 83: 157–169. 10.1016/j.ajhg.2008.06.021View ArticlePubMedGoogle Scholar
- Gonzalez E, Kulkarni H, Bolivar H, Mangano A, Sanchez R, Catano G, Nibbs RJ, Freedman BI, Quinones MP, Bamshad MJ, Murthy KK, Rovin BH, Bradley W, Clark RA, Anderson SA, O'connell RJ, Agan BK, Ahuja SS, Bologna R, Sen L, Dolan MJ, Ahuja SK: The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility. Science 2005, 307: 1434–1440. 10.1126/science.1101160View ArticlePubMedGoogle Scholar
- McCarroll SA, Huett A, Kuballa P: Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's disease. Nature Genetics 2008, 40: 1107–1112. 10.1038/ng.215PubMed CentralView ArticlePubMedGoogle Scholar
- Rovelet-Lecrux A, Hannequin D, Raux G, Le Meur N, Laquerriere A, Vital A, Feuillette S, Brice A, Vercelletto M, Dubas F, Frebourg T, Campion D: APP locus duplication causes autosomal dominant early-onset alzheimer disease with cerebral amyloid angiopathy. Nature Genetics 2006, 38: 24–26. 10.1038/ng1718View ArticlePubMedGoogle Scholar
- Sebat J: Major changes in our DNA lead to major changes in our thinking. Nature Genetics 39: S3-S5.Google Scholar
- Singleton AB, Farrer M, Johnson J, Singleton A, Hague S, Kachergus J, Hulihan M, Peuralinna T, Dutra A, Nussbaum R, Lincoln S, Crawley A, Hanson M, Maraganore D, Adler C, Cookson MR, Muenter M, Baptista M, Miller D, Blancato J, Hardy J, Gwinn-Hardy K: alpha-Synuclein locus triplication causes Parkinson's disease. Science 2003, 302: 841. 10.1126/science.1090278View ArticlePubMedGoogle Scholar
- Shendure J, Ji H: Next-generation DNA sequencing. Nature Biotechnology 2008, 26: 1135–1143. 10.1038/nbt1486View ArticlePubMedGoogle Scholar
- Kidd JM, Cooper GM, Donahue WF, Hayden HS, Sampas N, Graves T, Hansen N, Teague B, Alkan C, Antonacci F, Haugen E, Zerr T, Yamada NA, Tsang P, Newman TL, Tuzun E, Cheng Z, Ebling HM, Tusneem N, David R, Gillett W, Phelps KA, Weaver M, Saranga D, Brand A, Tao W, Gustafson E, McKernan K, Chen L, Malig M, Smith JD, Korn JM, McCarroll SA, Altshuler DA, Peiffer DA, Dorschner M, Stamatoyannopoulos J, Schwartz D, Nickerson DA, Mullikin JC, Wilson RK, Bruhn L, Olson MV, Kaul R, Smith DR, Eichler EE: Mapping and sequencing of structural variation from eight human genomes. Nature 2008, 453: 56–64. 10.1038/nature06862PubMed CentralView ArticlePubMedGoogle Scholar
- McCarroll SA, Kuruvilla FG, Korn JM, Cawley S, Nemesh J, Wysoker A, Shapero MH, de Bakker PI, Maller JB, Kirby A, Elliott AL, Parkin M, Hubbell E, Webster T, Mei R, Veitch J, Collins PJ, Handsaker R, Lincoln S, Nizzari M, Blume J, Jones KW, Rava R, Daly MJ, Gabriel SB, Altshuler D: Integrated detection and population-genetic analysis of SNPs and copy number variation. Nature Genetics 2008, 40: 1166–1174. 10.1038/ng.238View ArticlePubMedGoogle Scholar
- Perry GH, Tchinda J, McGrath SD, Zhang J, Picker SR, Caceres AM, Iafrate AJ, Tyler-Smith C, Scherer SW, Eichler EE, Stone AC, Lee C: Hotspots for copy number variation in chimpanzees and humans. Proceedings of the National Academy of Sciences of the United States of America 2006, 103: 8006–8011. 10.1073/pnas.0602318103PubMed CentralView ArticlePubMedGoogle Scholar
- Redon R, Ishikawa S, Fitch KR, Feuk L, Perry GH, Andrews TD, Fiegler H, Shapero MH, Carson AR, Chen W, Cho EK, Dallaire S, Freeman JL, Gonzalez JR, Gratacos M, Huang J, Kalaitzopoulos D, Komura D, MacDonald JR, Marshall CR, Mei R, Montgomery L, Nishimura K, Okamura K, Shen F, Somerville MJ, Tchinda J, Valsesia A, Woodwark C, Yang F, Zhang J, Zerjal T, Zhang J, Armengol L, Conrad DF, Estivill X, Tyler-Smith C, Carter NP, Aburatani H, Lee C, Jones KW, Scherer SW, Hurles ME: Global variation in copy number in the human genome. Nature 2006, 444: 444–454. 10.1038/nature05329PubMed CentralView ArticlePubMedGoogle Scholar
- de Smith AJ, Tsalenko A, Sampas N, Scheffer A, Yamada NA, Tsang P, Ben-Dor A, Yakhini Z, Ellis RJ, Bruhn L, Laderman S, Froguel P, Blakemore AI: Array CGH analysis of copy number variation identifies 1284 new genes variant in healthy white males: implications for association studies of complex disease. Human Molecular Genetics 2007, 16: 2783–2794. 10.1093/hmg/ddm208View ArticlePubMedGoogle Scholar
- Conrad DF, Pinto D, Redon R, Feuk L, Gokcumen O, Zhang Y, Aerts J, Andrews TD, Barnes C, Campbell P, Fitzgerald T, Hu M, Ihm CH, Kristiansson K, Macarthur DG, Macdonald JR, Onyiah I, Pang AW, Robson S, Stirrups K, Valsesia A, Walter K, Wei J, Wellcome Trust Case Control Consortium, Tyler-Smith C, Carter NP, Lee C, Scherer SW, Hurles ME: Origins and functional impact of copy number variation in the human genome. Nature 2009, 464: 704–712.PubMed CentralView ArticlePubMedGoogle Scholar
- Emerson JJ, Cardoso-Moreira M, Borevitz JO, Long M: Natural selection shapes genome-wide patterns of copy-number polymorphism in drosophila melanogaster. Science 2008, 320: 1629–1632. 10.1126/science.1158078View ArticlePubMedGoogle Scholar
- Sabeti PC, Varilly P, Fry B, Lohmueller J, Hostetter E, Cotsapas C, Xie X, Byrne EH, McCarroll SA, Gaudet R, Schaffner SF, Lander ES, International HapMap Consortium, Frazer KA, Ballinger DG, Cox DR, Hinds DA, Stuve LL, Gibbs RA, Belmont JW, Boudreau A, Hardenbol P, Leal SM, Pasternak S, Wheeler DA, Willis TD, Yu F, Yang H, Zeng C, Gao Y, Hu H, et al.: Genome-wide detection and characterization of positive selection in human populations. Nature 2007, 449: 913–918. 10.1038/nature06250PubMed CentralView ArticlePubMedGoogle Scholar
- Kato M, Nakamura Y, Tsunoda T: MOCSphaser: a haplotype inference tool from a mixture of copy number variation and single nucleotide polymorphism data. Bioinformatics 2008, 24: 1645–1646. 10.1093/bioinformatics/btn242PubMed CentralView ArticlePubMedGoogle Scholar
- Wigginton JE, Cutler DJ, Abecasis GR: A Note on Exact Tests of Hardy-Weinberg Equilibrium. American Journal of Human Genetics 2005, 76: 887–893. 10.1086/429864PubMed CentralView ArticlePubMedGoogle Scholar
- Wang K, Chen Z, Tadesse MG, Glessner J, Grant SF, Hakonarson H, Bucan M, Li M: Modeling genetic inheritance of copy number variations. Nucleic Acids Research 2008, 36: e138. 10.1093/nar/gkn641PubMed CentralView ArticlePubMedGoogle Scholar
- Su SY, Asher JE, Jarvelin MR, Froguel P, Blakemore AI, Balding DJ, Coin LJ: Inferring combined CNV/SNP haplotypes from genotype data. Bioinformatics 2010, 26: 1437–1445. 10.1093/bioinformatics/btq157PubMed CentralView ArticlePubMedGoogle Scholar
- Alkan C, Kidd JM, Marques-Bonet T, Aksay G, Antonacci F, Hormozdiari F, Kitzman JO, Baker C, Malig M, Mutlu O, Sahinalp SC, Gibbs RA, Eichler EE: Personalized copy number and segmental duplication maps using next-generation sequencing. Nature Genetics 2009, 41: 1061–1067. 10.1038/ng.437PubMed CentralView ArticlePubMedGoogle Scholar
- Ortiz-Estevez M, Bengtsson H, Rubio A: ACNE: a summarization method to estimate allele-specific copy numbers for Affymetrix SNP arrays. Bioinformatics 2010, 26: 1827–1833. 10.1093/bioinformatics/btq300PubMed CentralView ArticlePubMedGoogle Scholar
- Huang YT, Zhang K, Chen T, Chao KM: Selecting additional tag SNPs for tolerating missing data in genotyping. BMC Bioinformatics 2005, 6: 263. 10.1186/1471-2105-6-263PubMed CentralView ArticlePubMedGoogle Scholar
- McCarroll SA, Hadnott TN, Perry GH, Sabeti PC, Zody MC, Barrett JC, Dallaire S, Gabriel SB, Lee C, Daly MJ, Altshuler DM, International HapMap Consortium: Common deletion polymorphisms in the human genome. Nature Genetics 2006, 38: 86–92. 10.1038/ng1696View ArticlePubMedGoogle Scholar
- Surakka I, Kristiansson K, Anttila V, Inouye M, Barnes C, Moutsianas L, Salomaa V, Daly M, Palotie A, Peltonen L, Ripatti S: Founder population-specific HapMap panel increases power in GWA studies through improved imputation accuracy and CNV tagging. Genome Research 2010, 20: 1344–1351. 10.1101/gr.106534.110PubMed CentralView ArticlePubMedGoogle Scholar
- Ting CK, Lin WT, Huang YT: Multi-objective tag SNPs selection using evolutionary algorithms. Bioinformatics 2010, 26(11):1446–1452. 10.1093/bioinformatics/btq158View ArticlePubMedGoogle Scholar
- International HapMap Consortium, Frazer KA, Ballinger DG, Cox DR, Hinds DA, Stuve LL, Gibbs RA, Belmont JW, Boudreau A, Hardenbol P, Leal SM, Pasternak S, Wheeler DA, Willis TD, Yu F, Yang H, Zeng C, Gao Y, Hu H, Hu W, Li C, Lin W, Liu S, Pan H, Tang X, Wang J, Wang W, Yu J, Zhang B, Zhang Q: A second generation human haplotype map of over 3.1 million SNPs. Nature 449: 851–862.Google Scholar
- Stephens M, Donnelly P: A comparison of bayesian methods for haplotype reconstruction from population genotype data. Am J Hum Genet 2003, 73: 1162–1169. 10.1086/379378PubMed CentralView ArticlePubMedGoogle Scholar
- Bansal V, Bafna V: HapCUT: an efficient and accurate algorithm for the haplotype assembly problem. Bioinformatics 2008, 24: i153-i159. 10.1093/bioinformatics/btn298View ArticlePubMedGoogle Scholar
- Coja-Oghlan A, Moore C, Sanwalani V: MAX k-CUT and approximating the chromatic number of random graphs. Proceedings of 30th Int Coll Automata, Languages and Programming (ICALP) 2003.Google Scholar
- Frieze A, Jerrum M: Improved approximation algorithms for MAX k-CUT and MAX BISECTION. Algoritmica 1997, 18.Google Scholar
- Linardopoulou EV, Williams EM, Fan Y, Friedman C, Young JM, Trask BJ: Human subtelomeres are hot spots of interchromosomal recombination and segmental duplication. Nature 2005, 437: 94–100. 10.1038/nature04029PubMed CentralView ArticlePubMedGoogle Scholar
- Watson SK, deLeeuw RJ, Horsman DE, Squire JA, Lam WL: Cytogenetically balanced translocations are associated with focal copy number alterations. Human Genetics 2007, 120: 795–805. 10.1007/s00439-006-0251-9View ArticlePubMedGoogle Scholar
- Huang YT, Chao KM, Chen T: An approximation algorithm for haplotype inference by pure parsimony. Journal of Computational Biology 2005, 12: 1261–1274. 10.1089/cmb.2005.12.1261View ArticlePubMedGoogle Scholar
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