- Software review
- Open Access
Nephele: genotyping via complete composition vectors and MapReduce
© Colosimo et al; licensee BioMed Central Ltd. 2011
- Received: 5 April 2011
- Accepted: 18 August 2011
- Published: 18 August 2011
Current sequencing technology makes it practical to sequence many samples of a given organism, raising new challenges for the processing and interpretation of large genomics data sets with associated metadata. Traditional computational phylogenetic methods are ideal for studying the evolution of gene/protein families and using those to infer the evolution of an organism, but are less than ideal for the study of the whole organism mainly due to the presence of insertions/deletions/rearrangements. These methods provide the researcher with the ability to group a set of samples into distinct genotypic groups based on sequence similarity, which can then be associated with metadata, such as host information, pathogenicity, and time or location of occurrence. Genotyping is critical to understanding, at a genomic level, the origin and spread of infectious diseases. Increasingly, genotyping is coming into use for disease surveillance activities, as well as for microbial forensics. The classic genotyping approach has been based on phylogenetic analysis, starting with a multiple sequence alignment. Genotypes are then established by expert examination of phylogenetic trees. However, these traditional single-processor methods are suboptimal for rapidly growing sequence datasets being generated by next-generation DNA sequencing machines, because they increase in computational complexity quickly with the number of sequences.
Nephele is a suite of tools that uses the complete composition vector algorithm to represent each sequence in the dataset as a vector derived from its constituent k-mers by passing the need for multiple sequence alignment, and affinity propagation clustering to group the sequences into genotypes based on a distance measure over the vectors. Our methods produce results that correlate well with expert-defined clades or genotypes, at a fraction of the computational cost of traditional phylogenetic methods run on traditional hardware. Nephele can use the open-source Hadoop implementation of MapReduce to parallelize execution using multiple compute nodes. We were able to generate a neighbour-joined tree of over 10,000 16S samples in less than 2 hours.
We conclude that using Nephele can substantially decrease the processing time required for generating genotype trees of tens to hundreds of organisms at genome scale sequence coverage.
- Avian Influenza
- Affinity Propagation
- Adjust Rand Index
- Cosine Distance
In the post-genomic era, as sequencing becomes ever cheaper and more routine, biological sequence analysis has provided many useful tools for the study and combat of infectious disease. These tools, which can include both experimental and computational methods, are important for molecular epidemiological studies [1–3], vaccine development [4–6], and microbial forensics [7–9]. One such method is genotyping, the grouping of samples based on their genetic sequence. This can be done experimentally [10–12] or computationally, either by identifying genetic signatures (nucleotide substrings which are only found in a single group of sequences) , or on the basis of genetic distance among the sequences [14–16]. These methods allow a researcher to split a group of sequences into distinct partitions for further analysis. In a forensics context, genotyping a sequence can yield clues on where the sequence comes from. In surveillance, genotyping can be used to examine the evolutionary footprint of a pathogen, for example, to identify areas where certain vaccines and other countermeasures should be used.
Sequence-based comparison involves three major steps. The first is to choose a set of sequences to study, based on some criteria, such as strain, time period or geographic region. Ideally, this set can be easily extracted from a well-populated reference database, containing not only the sequence data for the samples of interest, such as a particular serotype of Influenza, but also sufficient metadata. For infectious diseases, types of metadata include geospatial and temporal co-ordinates, host information, and pathogenicity. Once the appropriate dataset is chosen, the samples are compared and clustered in sequence space. From here, the metadata associated with the sequences is used to assess the evolutionary landscape of the organism or pathogen .
Sequence Comparison Methods
Traditionally, the first step in performing sequence comparisons is to generate a multiple sequence alignment (MSA) from the sequences of interest. This is most often done using heuristics found in utilities such as CLUSTAL W , MUSCLE , T-COFFEE , and ProbCons . The dynamic programming solution, which can find the mathematically but not necessarily biologically correct solution, quickly becomes impractical with the sample sizes used in any meaningful analysis. A recent review  examined many of the issues in producing these alignments, most notably the trade-offs between alignment accuracy, time, and computational expense. Many of the most accurate algorithms cannot be used on a large number of sequences, or on very lengthy sequences, and were only recommended for sets of less than 100 sequences.
Because the alignment is dependent on each of the sequences from which it is calculated, the alignment must be recomputed whenever a new sequence is added. This becomes problematic for surveillance applications, where new sequences will be added constantly. While this problem has been mitigated to some extent using with algorithms such as Near-Alignment Space Termination (NAST) , this still adds a level of complexity if the dataset is continually growing, as is the case with Influenza and other infectious diseases. Another issue is that different heuristics will yield different alignments -- they are only designed to find an acceptable answer, not the optimal alignment. While methods have been developed to find a "consensus alignment"  from a set of alignments, this requires a good deal of time and computing power.
The composition vector (CV)  method has been used to describe DNA/RNA and protein sequences as vectors, using the distance between these vectors as the genetic distance. This method involves using a sliding window to represent each sequence as a vector, where each element of the vector is calculated based on the actual and expected frequency of the k-mer (DNA/protein subsequence of length k) observed in that window. The vector representation allows the distance between two sequences to be calculated with any standard distance metric. The CV method was shown to produce trees which matched established taxonomies, as inferred from the 16S RNA segment by more conventional alignment-based methods . The CV method was later expanded into the complete composition vector (CCV) method , which uses sliding windows over a range of lengths to describe the sequence. Since these methods do not require alignments to be calculated, distances calculated between sequences remain constant, rather than being dependent on the set of sequences being examined, making these methods ideal for the handling of rapidly growing datasets. No molecular models need be used to calculate distances -- distances are calculated using any distance metric that can be used to calculate the distance between vectors.
The next step in sequence analysis is the clustering of the sequences. Traditionally, this is done by inferring a phylogenetic tree. Tools for this purpose include PHYLIP , PAUP* , or POY . This work was initially performed using distance-based methods, such as the UPGMA or neighbour-joining algorithms , or cladistic methods such as Maximum Parsimony. As computational power increased, methods that inferred trees based on models of evolution were used. These include the Maximum Likelihood technique, as well as Bayesian Inference. While these methods produce phylogenetic trees, which provide a useful visualization, any further analysis and grouping must be performed manually. As the number of sequences to compare increases, this becomes more and more difficult. In fact, there has been much recent research into new methods to visualize phylogenetic trees with large numbers of leaves [32, 33]. In addition, the phylogenetic tree view proves difficult to integrate with the metadata. For example, a recent paper discussing the spread of H5N1 Avian Influenza used Google Earth to draw a phylogenetic tree on top of the globe . While this visualization works well for a small number of samples, it is ineffective for larger datasets, due to the "busyness" of the visualization.
An alternative to the pure phylogenetic approach is computational genotyping. This involves partitioning the set of sequences into discrete groups, based on some criteria. This can be based on differences between known subtypes, such as tandem repeats or single nucleotide polymorphisms, or by genetic distance. In the case of genotyping based on distance, this becomes a clustering problem. In 2007, Frey and Dueck published a paper on a new clustering algorithm known as affinity propagation clustering . In contrast to other clustering algorithms, such as k-means and Expectation Maximization (EM), the affinity propagation algorithm does not require the user to explicitly select a given number of exemplars at the start of clustering. Instead, affinity propagation simultaneously considers all points as potential exemplars, using an initial preference to determine the sensitivity, and therefore the number of clusters. This eliminates the need for large numbers of runs to determine the ideal number of clusters and any dependence on initial conditions seen in other partition clustering algorithms. Furthermore, this algorithm allows the user to set the preference for each data point. This is useful for a scenario where a partial set of representative samples are known, but there may be other exemplars along with these in a data set. The affinity propagation has been tested on geospatial, text, and gene expression data and showed improvements in both speed and accuracy over other clustering algorithms.
The main advantage of an automated computational genotyping method is that it gives the researcher the ability to combine a measure of sequence similarity (cluster membership) with the metadata. It is this metadata that yields the most information about a sample. A phylogenetic tree will tell what samples are close in sequence space, but any further inference is made using the metadata. By separating the sequences into discrete groups, the researcher is given much more flexibility to visualize the data and associated metadata.
MapReduce  is the software framework developed by Google™ to support parallel distributed execution of their data intensive applications. MapReduce is designed for fault-tolerant computations with extremely large datasets. MapReduce is divided into two major phases called map and reduce, separated by an internal shuffle phase of the intermediate results. Hadoop is an open-source version of MapReduce implemented in Java and sponsored by Amazon™, Yahoo™, and other major vendors. Recently, MapReduce has been used for sequence and phylogenetic applications. For example, CloudBurst uses Hadoop for parallel short read-mapping for use in a variety of biological analyses including SNP discovery, genotyping, and personal genomics . The Genome Analysis Toolkit uses the MapReduce paradigm for shared memory platforms . MrsRF (MapReduce Speeds up RF) is a multi-core, multi-machine algorithm that generates t × t Robinson-Foulds distance matrix between t trees  using Phoenix , a MapReduce implementation for shared memory multi-core platform, and OpenMPI . These uses indicate that MapReduce is a promising tool to help solve the computational challenges with large datasets.
In this paper, we describe a scalable complete genotyping system that brings together the complete composition vector and affinity propagation algorithms to produce genotypes from Influenza A sequences. The system has been tested on a variety of Influenza A and Actinomycetes genome data. In addition to providing discrete clusters representing genotypes, we use methods that produce trees that closely match the topologies of trees inferred using traditional phylogenetic methods, in order to provide scientists with a more familiar visualization.
The Influenza dataset used to develop our methods was that of Holmes et al. . The clades and reassortment events found in these samples were discussed in detail, providing eight sets of sequences (one for each gene studied in the paper) for verification of our methods. This dataset consists of 155 samples, taken from New York State during the 1999-2000, 2001-2002, 2002-2003, and 2003-2004 flu seasons. The complete coding sequences are available, as well as the date and county of collection for these strains. We also used HA segments from H1N1 (1141) and H3N2 (2201) parsed from GenBank's viral division (gbvrl). For testing our implementation, we used 10,270 16S samples from GreenGenes (core_set_aligned.fasta retired on 07 February 2007; http://greengenes.lbl.gov/).
To test our methods, two additional datasets were identified. A set of 94 sequences representing WHO expert-defined genotypes (http://www.who.int/csr/disease/avian_influenza/guidelines/nomenclature/) was used to validate our methods, and another dataset representing an 2007 Influenza outbreak in Europe was chosen to demonstrate the utility of the computational genotyping approach for microbial forensic analysis (Additional File 1).
We also used 27 full length genomes of Actinomycetes bacteria from the Broad Institute along with their computed concatenated protein sequences, downloaded from the Tuberculosis Database (TBDB) .
Complete Composition Vector
This is designed to highlight the role of selective mutation, and it was found that phylogenetic trees produced without subtracting the background via the Markov model were not consistent with traditional approaches .
The kth composition vector, Vk(S), is comprised of the composition values for all possible substrings of length k. For amino acid sequences, V is of length 20 k, and for DNA/RNA, V is of length 4 k. This method has been shown to produce trees which match known taxonomies .
In 2004, Wu et al. extended the CV approach into the complete composition vector (CCV) . This method combines the composition vector approach with the idea of the complete information set, in order to supplement any information loss from the background subtraction in the CV method . The CCV is defined as the sequence of composition vectors from 3 to M, where M is a pre-determined constant.
where Π represents the complete composition vector calculated from the concatenation of all n sequences in the dataset. In summary, this method evaluates the information content associated with each possible substring, and the most informative substrings are chosen for inclusion in the analysis. The number of n-mers used for distance calculations was chosen based on the dataset: if the absolute revised relative entropy was below 1.0, the substring was not used for any further calculations.
Affinity Propagation Clustering
Where ai is the sample's average distance to the other samples in its cluster and bi is the minimum average distance between the sample and the samples in each of the other clusters. The developers of the algorithm recommend using the minimum similarity between samples for a low number of clusters, and the median similarity for a moderate number of clusters. The preference resulting in the optimal partitioning, using the average silhouette value as a measurement was chosen from a set of four preferences spanning the minimum and median similarity. Affinity propagation was performed using the MATLAB function available at the authors' website (http://www.psi.toronto.edu/affinitypropagation/), with the default parameters or with our re-implementation written in Java as part of Nephele.
Parallelization with Hadoop
We also implemented most of our CCV code for execution as a series of nine MapReduce jobs using the open-source MapReduce implementation Hadoop (http://hadoop.apache.org/). MapReduce is not ideal for the generation of neighbour-joined trees or affinity propagation. The MapReduce paradigm depends on the maps not dependent on any other data than what they are given. Both the neighbour-joined trees and affinity propagation algorithms depend on shared states, which breaks the MapReduce paradigm. However, Nephele provides a Message Passing Interface (MPI) version of Panjo, a neighbour-joining algorithm, that is able to handle very large trees . Our version accepts row packed matrices instead of column packed, because it was easier to generate them as opposed to column packed matrices using MapReduce. All experiments were run on a Rocks (http://www.rocksclusters.org/) cluster running CentOS 5.4 on Intel Core 2 Quad and Core 2 Duo processors with 8 and 4 GB of memory, respectively, using Java 1.5 and Hadoop 0.20.1.
Genotyping the New York Dataset: Results, Computation Time and Choice of Distance Metric
The dataset used by Holmes and colleagues to study reassortment events throughout New York State provided a dataset to use to build and refine the genotyping methods. This set included 155 full genomes of H3N2 found in New York state between 1999 and 2004, collected as part of the Influenza Genome Sequencing Initiative , a worldwide sequencing initiative (this project has also sampled from the southern hemisphere, in Australia and New Zealand). Since the complete genome for each of the samples in this set was sequenced, this provided genes, with differing rates of evolution to test the pipeline.
Clustering was performed on the eight genes studied in detail in the paper (HA, M1, NA, NP, NS1, PA, PB1, PB2) as described in the Implementation section. Cluster counts ranged from 5 (NP, PB2) to 15 (PB1), with clusters ranging in size from 1 (representing an outlier in the dataset) to 36. The results from the affinity propagation clustering matched the clade structure of the trees. The trees for all eight genes, colored by cluster membership, can be seen in Additional File 2. All phylogenetic trees in this work were produced using TreeViewJ . The segmented nature of the Influenza genome adds a level of complexity to the genotyping problem. For each sample, the set of clusters for the eight genes can be used to define a cluster "profile," which represents the genotype defined by the complete genome for that sample. This profile represents the composite genotype for that sample. For the 155 samples in the dataset, 32 genotypes were identified. From these, the groups of samples identified by Holmes and colleagues to be involved in reassortment events were found as distinct genotypes.
One of the major advantages of the complete composition vector approach over traditional phylogenetic methods is the speed of analysis. For the individual gene segments in the test dataset (155 sequences), execution times ranged from 1.50 minutes (M1) to 2.25 minutes (NA) In contrast, alignment times using MUSCLE were on the order of 5-10 minutes, and inference of maximum likelihood trees took roughly 20 minutes per gene If the genes are concatenated together to create a full genome sequence, the gains are even more impressive -- trees were produced in a few minutes with the CCV-based approach, rather than hours for traditional alignment-based methods. This is consistent with initial results from composition vector based approaches, which focused on inferring trees for complete prokaryotic genomes .
Clustering on H5N1 Standard Nomenclature Dataset for Validation
In 2001, the World Health Organization (WHO), along with the World Organization for Animal Health (OIE) and Food and Agriculture Organization of the United Nations (FAO) released, in poster form, a standard nomenclature system for the various lineages of Influenza H5N1 found in over 50 countries throughout the world This nomenclature is intended to replace the current nomenclature used in publications, where samples are often identified by the location of the earliest sample with the closest genetic similarity (for example, "Fujian-like" or "Quinghai lineage"). Alignments of 904 HA sequences were created, and clades were chosen from the tree based on a set of rules. These clades, developed to define a new standard nomenclature, provided an opportunity to blind test set our genotyping system.
We also performed a detailed examination of the trees produced by the CCV method with those from the study. We found that members of Clade 2.3.1 were found in two distinct groups on our tree, one of which was quite distant from the rest of the samples in the tree. Upon looking at the sequences, we found that these were much shorter (~1000 bp) than the rest of the sequences (~1600 bp), indicating that these sequences were most likely HA1 sequences, rather than the full HA coding sequence, even though they were labelled full HA. This highlights a problem with the quality of data that currently exists in the databases. These inconsistencies in the data can significantly distort the results of the various sequence analysis methods.
We investigated is our implementation can be used for larger and more complex genomes. We acquired 27 full length Actinomycetes genomes from the Tuberculosis Database at the Broad Institute and ran them through our pipeline. We were able to produce trees that had the same topology as those generated by the Broad in about 30 minutes compared to several hours for them using traditional tools (Brian Weiner, personal communication, from unpublished data). In addition, we compared the trees produced using the concatenation of the predicted proteins of the same set of genomes and we got similar results in both time to produce and the topology of the trees. However, it should be noted that the length of the branches are different.
During the development of the CCV code, we ran into memory bottle necks that required extensive coding to minimize. In addition, it was noted that several of the steps could be parallelized. We examined Hadoop to determine if we could utilize it for parallelizing our code across commodity hardware in a fault-tolerant way. We were able to code most of our algorithms using Hadoop. The few that we did not code were the neighbour-joining tree and the affinity propagation clustering algorithms. We provide a modified version of Panjo , a neighbour-joining algorithm, that uses the output of our Hadoop cosine distance matrix, which is in row major (packed) order. We also can output the matrix in the Phylip square format. We were able to generate a neighbour-joined tree for 10,270 16S samples in 106 minutes using our Rocks Cluster of 30 machines, which we were not able to compute at all using our code on a single machine.
Project name: Nephele
Project home page: http://code.google.com/p/nephele/
Operating system: Linux, Mac OS X, Unix
Programming language: Java and C
License: Apache License 2.0
This work was funded through the MITRE Internal Research Program. Approved for Public Release: 10-9999. Distribution Unlimited.
- Li KS, Guan Y, Wang J, Smith GJ, Xu KM, Duan L, Rahardjo AP, Puthavathana P, Buranathai C, Nguyen TD, et al: Genesis of a highly pathogenic and potentially pandemic H5N1 influenza virus in eastern Asia. Nature. 2004, 430: 209-213. 10.1038/nature02746.View ArticlePubMedGoogle Scholar
- Campitelli L, Di Martino A, Spagnolo D, Smith GJ, Di Trani L, Facchini M, De Marco MA, Foni E, Chiapponi C, Martin AM, et al: Molecular analysis of avian H7 influenza viruses circulating in Eurasia in 1999-2005: detection of multiple reassortant virus genotypes. J Gen Virol. 2008, 89: 48-59. 10.1099/vir.0.83111-0.View ArticlePubMedGoogle Scholar
- Rambaut A, Pybus OG, Nelson MI, Viboud C, Taubenberger JK, Holmes EC: The genomic and epidemiological dynamics of human influenza A virus. Nature. 2008, 453: 615-619. 10.1038/nature06945.PubMed CentralView ArticlePubMedGoogle Scholar
- De Groot AS, Bosma A, Chinai N, Frost J, Jesdale BM, Gonzalez MA, Martin W, Saint-Aubin C: From genome to vaccine: in silico predictions, ex vivo verification. Vaccine. 2001, 19: 4385-4395. 10.1016/S0264-410X(01)00145-1.View ArticlePubMedGoogle Scholar
- Yang HL, Zhu YZ, Qin JH, He P, Jiang XC, Zhao GP, Guo XK: In silico and microarray-based genomic approaches to identifying potential vaccine candidates against Leptospira interrogans. BMC Genomics. 2006, 7: 293-10.1186/1471-2164-7-293.PubMed CentralView ArticlePubMedGoogle Scholar
- Macken C, Lu H, Goodman J, Boykin L: The value of a database in surveillance and vaccine selection. International Congress Series. 2001, 1219: 103-106.View ArticleGoogle Scholar
- Cummings CA, Relman DA: Genomics and microbiology. Microbial forensics--"cross-examining pathogens". Science. 2002, 296: 1976-1979. 10.1126/science.1073125.View ArticlePubMedGoogle Scholar
- Budowle B, Schutzer SE, Ascher MS, Atlas RM, Burans JP, Chakraborty R, Dunn JJ, Fraser CM, Franz DR, Leighton TJ, et al: Toward a system of microbial forensics: from sample collection to interpretation of evidence. Appl Environ Microbiol. 2005, 71: 2209-2213. 10.1128/AEM.71.5.2209-2213.2005.PubMed CentralView ArticlePubMedGoogle Scholar
- McEwen SA, Wilson TM, Ashford DA, Heegaard ED, Kournikakis B: Microbial forensics for natural and intentional incidents of infectious disease involving animals. Rev Sci Tech. 2006, 25: 329-339.PubMedGoogle Scholar
- Wang D, Coscoy L, Zylberberg M, Avila PC, Boushey HA, Ganem D, DeRisi JL: Microarray-based detection and genotyping of viral pathogens. Proc Natl Acad Sci USA. 2002, 99: 15687-15692. 10.1073/pnas.242579699.PubMed CentralView ArticlePubMedGoogle Scholar
- Ghindilis AL, Smith MW, Schwarzkopf KR, Roth KM, Peyvan K, Munro SB, Lodes MJ, Stover AG, Bernards K, Dill K, McShea A: CombiMatrix oligonucleotide arrays: genotyping and gene expression assays employing electrochemical detection. Biosens Bioelectron. 2007, 22: 1853-1860. 10.1016/j.bios.2006.06.024.View ArticlePubMedGoogle Scholar
- Lindh M, Andersson AS, Gusdal A: Genotypes, nt 1858 variants, and geographic origin of hepatitis B virus--large-scale analysis using a new genotyping method. J Infect Dis. 1997, 175: 1285-1293. 10.1086/516458.View ArticlePubMedGoogle Scholar
- Lin G, Cai Z, Wu J, Wan XF, Xu L, Goebel R: Identifying a few foot-and-mouth disease virus signature nucleotide strings for computational genotyping. BMC Bioinformatics. 2008, 9: 279-10.1186/1471-2105-9-279.PubMed CentralView ArticlePubMedGoogle Scholar
- Lu G, Rowley T, Garten R, Donis RO: FluGenome: a web tool for genotyping influenza A virus. Nucleic Acids Res. 2007, 35: W275-279. 10.1093/nar/gkm365.PubMed CentralView ArticlePubMedGoogle Scholar
- Wan XF, Chen G, Luo F, Emch M, Donis R: A quantitative genotype algorithm reflecting H5N1 Avian influenza niches. Bioinformatics. 2007, 23: 2368-2375. 10.1093/bioinformatics/btm354.View ArticlePubMedGoogle Scholar
- Stuyver L, De Gendt S, Van Geyt C, Zoulim F, Fried M, Schinazi RF, Rossau R: A new genotype of hepatitis B virus: complete genome and phylogenetic relatedness. J Gen Virol. 2000, 81: 67-74.View ArticlePubMedGoogle Scholar
- Colosimo M, Hirschman L, Keybl M, Luciano J, Mardis S, Peterson M: Genomics For Bioforensics: MITRE Sponsored Research Final Report. 2008, Bedford, MA: The MITRE CorporationGoogle Scholar
- Thompson JD, Higgins DG, Gibson TJ: CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Res. 1994, 22: 4673-4680. 10.1093/nar/22.22.4673.PubMed CentralView ArticlePubMedGoogle Scholar
- Edgar RC: MUSCLE: a multiple sequence alignment method with reduced time and space complexity. BMC Bioinformatics. 2004, 5: 113-10.1186/1471-2105-5-113.PubMed CentralView ArticlePubMedGoogle Scholar
- Notredame C, Higgins DG, Heringa J: T-Coffee: A novel method for fast and accurate multiple sequence alignment. J Mol Biol. 2000, 302: 205-217. 10.1006/jmbi.2000.4042.View ArticlePubMedGoogle Scholar
- Do CB, Mahabhashyam MS, Brudno M, Batzoglou S: ProbCons: Probabilistic consistency-based multiple sequence alignment. Genome Res. 2005, 15: 330-340. 10.1101/gr.2821705.PubMed CentralView ArticlePubMedGoogle Scholar
- Edgar RC, Batzoglou S: Multiple sequence alignment. Curr Opin Struct Biol. 2006, 16: 368-373. 10.1016/j.sbi.2006.04.004.View ArticlePubMedGoogle Scholar
- DeSantis TZ, Hugenholtz P, Keller K, Brodie EL, Larsen N, Piceno YM, Phan R, Andersen GL: NAST: a multiple sequence alignment server for comparative analysis of 16S rRNA genes. Nucleic Acids Res. 2006, 34: W394-399. 10.1093/nar/gkl244.PubMed CentralView ArticlePubMedGoogle Scholar
- Wallace IM, O'Sullivan O, Higgins DG, Notredame C: M-Coffee: combining multiple sequence alignment methods with T-Coffee. Nucleic Acids Res. 2006, 34: 1692-1699. 10.1093/nar/gkl091.PubMed CentralView ArticlePubMedGoogle Scholar
- Chu KH, Qi J, Yu ZG, Anh V: Origin and phylogeny of chloroplasts revealed by a simple correlation analysis of complete genomes. Mol Biol Evol. 2004, 21: 200-206.View ArticlePubMedGoogle Scholar
- Gao L, Qi J, Sun J, Hao B: Prokaryote phylogeny meets taxonomy: An exhaustive comparison of composition vector trees with systematic bacteriology. Sci China C Life Sci. 2007, 50: 587-599. 10.1007/s11427-007-0084-3.View ArticlePubMedGoogle Scholar
- Wu X, Wan X-F, Wu G, Xu D, Lin G: Whole Genome Phyogeny via Complete Composition Vectors. Technical Report TR05-06. 2005, Department of Computing Science, University of AlbertaGoogle Scholar
- Retief JD: Phylogenetic analysis using PHYLIP. Methods Mol Biol. 2000, 132: 243-258.PubMedGoogle Scholar
- Wilgenbusch JC, Swofford D: Inferring evolutionary trees with PAUP*. Curr Protoc Bioinformatics. 2003, 6: Unit 6 4Google Scholar
- Giribet G: Exploring the behavior of POY, a program for direct optimization of molecular data. Cladistics. 2001, 17: S60-70. 10.1111/j.1096-0031.2001.tb00105.x.View ArticlePubMedGoogle Scholar
- Saitou N, Nei M: The neighbor-joining method: a new method for reconstructing phylogenetic trees. Mol Biol Evol. 1987, 4: 406-425.PubMedGoogle Scholar
- Rost U, Bornberg-Bauer E: TreeWiz: interactive exploration of huge trees. Bioinformatics. 2002, 18: 109-114. 10.1093/bioinformatics/18.1.109.View ArticlePubMedGoogle Scholar
- Hughes T, Hyun Y, Liberles DA: Visualising very large phylogenetic trees in three dimensional hyperbolic space. BMC Bioinformatics. 2004, 5: 48-10.1186/1471-2105-5-48.PubMed CentralView ArticlePubMedGoogle Scholar
- Janies D, Hill AW, Guralnick R, Habib F, Waltari E, Wheeler WC: Genomic analysis and geographic visualization of the spread of avian influenza (H5N1). Syst Biol. 2007, 56: 321-329. 10.1080/10635150701266848.View ArticlePubMedGoogle Scholar
- Frey BJ, Dueck D: Clustering by passing messages between data points. Science. 2007, 315: 972-976. 10.1126/science.1136800.View ArticlePubMedGoogle Scholar
- Dean J, Ghemawat S: MapReduce: simplified data processing on large clusters. Proceedings of the 6th conference on Symposium on Opearting Systems Design\& Implementation - Volume 6. 2004, San Francisco, CA: USENIX AssociationGoogle Scholar
- Schatz MC: CloudBurst: highly sensitive read mapping with MapReduce. Bioinformatics. 2009, 25: 1363-1369. 10.1093/bioinformatics/btp236.PubMed CentralView ArticlePubMedGoogle Scholar
- McKenna A, Hanna M, Banks E, Sivachenko A, Cibulskis K, Kernytsky A, Garimella K, Altshuler D, Gabriel S, Daly M, DePristo MA: The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. Genome Res. 2010, 20: 1297-1303. 10.1101/gr.107524.110.PubMed CentralView ArticlePubMedGoogle Scholar
- Matthews SJ, Williams TL: MrsRF: an efficient MapReduce algorithm for analyzing large collections of evolutionary trees. BMC Bioinformatics. 2010, 11 (Suppl 1): S15-10.1186/1471-2105-11-S1-S15.PubMed CentralView ArticlePubMedGoogle Scholar
- Ranger C, Raghuraman R, Penmetsa A, Bradski G, Kozyrakis C: Evaluating MapReduce for Multi-core and Multiprocessor Systems. High Performance Computer Architecture, 2007 HPCA 2007 IEEE 13th International Symposium on. 2007, 13-24.View ArticleGoogle Scholar
- Gabriel E, Fagg GE, Bosilca G, Angskun T, Dongarra JJ, Squyres JM, Sahay V, Kambadur P, Barrett B, Lumsdaine A: Open MPI: Goals, Concept, and Design of a Next Generation MPI Implementation. Proceedings, 11th European PVM/MPI Users' Group Meeting, Budapest, Hungary. 2004, 97-104.Google Scholar
- Holmes EC, Ghedin E, Miller N, Taylor J, Bao Y, St George K, Grenfell BT, Salzberg SL, Fraser CM, Lipman DJ, Taubenberger JK: Whole-genome analysis of human influenza A virus reveals multiple persistent lineages and reassortment among recent H3N2 viruses. PLoS Biol. 2005, 3: e300-10.1371/journal.pbio.0030300.PubMed CentralView ArticlePubMedGoogle Scholar
- Reddy TB, Riley R, Wymore F, Montgomery P, DeCaprio D, Engels R, Gellesch M, Hubble J, Jen D, Jin H, et al: TB database: an integrated platform for tuberculosis research. Nucleic Acids Res. 2009, 37: D499-508. 10.1093/nar/gkn652.PubMed CentralView ArticlePubMedGoogle Scholar
- Wu X, Cai Z, Wan XF, Hoang T, Goebel R, Lin G: Nucleotide composition string selection in HIV-1 subtyping using whole genomes. Bioinformatics. 2007, 23: 1744-1752. 10.1093/bioinformatics/btm248.View ArticlePubMedGoogle Scholar
- Brendel V, Beckmann JS, Trifonov EN: Linguistics of nucleotide sequences: morphology and comparison of vocabularies. J Biomol Struct Dyn. 1986, 4: 11-21.View ArticlePubMedGoogle Scholar
- Li M, Fang W, Ling L, Wang J, Xuan Z, Chen R: Phylogeny based on whole genome as inferred from complete infomration set analysis. Journal of Biological Physics. 2002, 439-447.Google Scholar
- Bullard J: panjo: a parallel neighbor joining algorithm. 2007, BerkeleyGoogle Scholar
- Fauci AS: Race against time. Nature. 2005, 435: 423-424. 10.1038/435423a.View ArticlePubMedGoogle Scholar
- Peterson MW, Colosimo ME: TreeViewJ: an application for viewing and analyzing phylogenetic trees. Source Code Biol Med. 2007, 2: 7-10.1186/1751-0473-2-7.PubMed CentralView ArticlePubMedGoogle Scholar
- Drummond A, Strimmer K: PAL: an object-oriented programming library for molecular evolution and phylogenetics. Bioinformatics. 2001, 17: 662-663. 10.1093/bioinformatics/17.7.662.View ArticlePubMedGoogle Scholar
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