- Methodology article
- Open Access
WiseScaffolder: an algorithm for the semi-automatic scaffolding of Next Generation Sequencing data
BMC Bioinformatics volume 16, Article number: 281 (2015)
The sequencing depth provided by high-throughput sequencing technologies has allowed a rise in the number of de novo sequenced genomes that could potentially be closed without further sequencing. However, genome scaffolding and closure require costly human supervision that often results in genomes being published as drafts. A number of automatic scaffolders were recently released, which improved the global quality of genomes published in the last few years. Yet, none of them reach the efficiency of manual scaffolding.
Here, we present an innovative semi-automatic scaffolder that additionally helps with chimerae resolution and generates valuable contig maps and outputs for manual improvement of the automatic scaffolding. This software was tested on the newly sequenced marine cyanobacterium Synechococcus sp. WH8103 as well as two reference datasets used in previous studies, Rhodobacter sphaeroides and Homo sapiens chromosome 14 (http://gage.cbcb.umd.edu/). The quality of resulting scaffolds was compared to that of three other stand-alone scaffolders: SSPACE, SOPRA and SCARPA. For all three model organisms, WiseScaffolder produced better results than other scaffolders in terms of contiguity statistics (number of genome fragments, N50, LG50, etc.) and, in the case of WH8103, the reliability of the scaffolds was confirmed by whole genome alignment against a closely related reference genome. We also propose an efficient computer-assisted strategy for manual improvement of the scaffolding, using outputs generated by WiseScaffolder, as well as for genome finishing that in our hands led to the circularization of the WH8103 genome.
Altogether, WiseScaffolder proved more efficient than three other scaffolders for both prokaryotic and eukaryotic genomes and is thus likely applicable to most genome projects. The scaffolding pipeline described here should be of particular interest to biologists wishing to take advantage of the high added value of complete genomes.
The drastic reduction of cost associated with Next Generation Sequencing (NGS) technologies has revolutionized the field of genomics, granting researchers an easy access to new genomes . However, while complete genomes were a gold standard until the end of the 2000’s, the recent exponential increase of the number of sequenced genomes came along with a dramatic rise in the proportion of draft genomes since 2010 (; see also http://www.genomesonline.org/statistics ). Draft genomes may be sufficient for some applications, such as population genomics or multi-locus analyses. Still, the availability of complete genomes remains highly valuable when all the genes of an organism need to be properly identified. This is for instance the case in comparative genomic studies, where it is necessary to determine the pan, core and accessory genomes, or in the identification of genomic islands, which may be involved in pathogenicity and/or adaptation to specific ecological niches. In this context, bioinformaticians constantly have to adapt algorithms and pipelines to the rapidly evolving sequencing technologies, which generate genomic data with ever-increasing read length and sequencing depth, in order to successfully address issues raised by genome assembly and scaffolding.
Most recent de novo assemblers, such as VELVET [3, 4] or CLC AssemblyCell© (CLC Bio, Aarhus, Denmark) are able to use paired reads, with short or long inserts (i.e., pair-ends or mate-pairs, hereafter PE and MP, respectively) to assemble reads into contigs containing gaps filled with a number of Ns that is based on the average insert size of the PE and/or MP libraries. Although the use of paired reads generally improves the quality of the assembly, the simultaneous use of the sequences and insert sizes information shows some limitations for both library types. Indeed, although PE libraries allow one to get longer reads, and therefore improve local assembly, they do not permit to connect regions a few thousands nucleotides apart. While MPs allow to do so, generation of such long-insert libraries remains technically challenging, often resulting in large insert size variability [5–7], leading to an approximate number of Ns within contigs.
An alternative solution to the concomitant treatment of local and distant assembly is to perform consecutively the assembly into contigs, using single or PE reads, then scaffolding, i.e. ordering and merging contigs into scaffolds, using paired reads. The latter step is addressed by several stand-alone scaffolders such as Bambus , SSPACE , SOPRA , MIP Scaffolder  and, more recently, SCARPA . The strategy adopted by the greedy algorithms Bambus and SSPACE consists in ordering contigs based on the number of links that associates them, while other scaffolders use more sophisticated algorithms to explore a graph where nodes and edges are contigs and pairs of reads linking them, respectively. Although most of these scaffolders are able to automatically produce a manageable number of scaffolds, none of them is able to generate a single scaffold. Indeed, numerous genomic features, essentially related to repeats (e.g., multi-copy genes, homopolymers, etc.), are either difficult to reconstruct in silico or simply difficult to sequence, resulting in either gaps, chimerae or collapsed repeats in the genomic sequence that may lead to erroneous decisions during the manual finishing. Moreover, most stand-alone scaffolders are tricky to install and/or run and can require significant work to prepare input files . At last, although scaffolding lowers the number of chromosome (Chr.) fragments, it does not avoid the need for genome finishing, a step during which gaps created through scaffolding are closed and local polymorphism associated with multi-copy genes is resolved. Altogether, these time-consuming steps might be discouraging and often result into genomes being published as drafts .
In the context of a large marine Synechococcus genome sequencing project ( http://application.sb-roscoff.fr/cyanorak/ ), we developed WiseScaffolder, an innovative bioinformatic tool that mimicks progressive manual scaffolding using a greedy, iterative reconstruction of contigs neighborhood (Fig. 1). Based on a simple set of rules, WiseScaffolder efficiently addresses such scaffolding issues as chimerae and multi-copy contigs. Besides semi-automatically generating high quality scaffolds, it also provides valuable data to manually improve the scaffolding and also useful for genome finishing. Here, the efficiency of WiseScaffolder was tested on one of the newly sequenced genomes of marine cyanobacteria, Synechococcus sp. WH8103 (hereafter WH8103), as well as on two additional datasets from the GAGE study (Genome Assembly Gold-Standard Evaluation; ), Rhodobacter sphaeroides and Homo sapiens Chr.14, representatives of the prokaryotic and eukaryotic domains, respectively. Quality of the results were compared to those obtained with three other stand-alone scaffolders (SCARPA, SOPRA and SSPACE) using QUAST  and other comparative genomic tools.
Results and discussion
Comparison of WiseScaffolder with other scaffolders
The recent advent of NGS technologies has triggered the development of a number of stand-alone scaffolders, the relative efficiency of which may be tricky to assess for bioanalysts and is highly dataset dependent. For instance, the E. coli strain K-12 substrain MG1655 dataset that was used to compare the recently published SCARPA to several other scaffolders , might be misleading because the assembly of such low quality data (insert size ~200 bp, reads ~36 bp) generally results into short contigs that are challenging to scaffold, whatever the efficiency of the scaffolder. Here, we rather chose to compare recent and/or widely used scaffolders using three genome datasets that were assembled from reads sequenced by Illumina with up-to-date performance (i.e., 101 bp paired reads, Table 1). These include the newly sequenced Synechococcus sp. WH8103 genome (42 contigs assembled using the CLC assembler; MP library insert size ~4 kb) as well as two reference datasets retrieved from the GAGE study , namely R. sphaeroides (177 Bambus2-assembled contigs ; MP library insert size ~3.5 kb) and Homo sapiens Chr.14 (3,541 CABOG-assembled contigs ; MP library insert size: 2.3-2.8 kb).
To assess the efficiency of WiseScaffolder, the abovementioned datasets were scaffolded using three other stand-alone scaffolders: SSPACE , SOPRA  and SCARPA . Results of this benchmark are shown in Table 2. Additionally, for WH8103, we also tested the simultaneous assembly and scaffolding functions of the CLC assembler by assembling MP reads with distance constraint. In the case of the cyanobacterial genome, CLC assembly of MPs proved much less efficient in terms of scaffolds number and size than the stand-alone scaffolders and was thus not further considered in the benchmarking. For all datasets, WiseScaffolder produced better results than the three other scaffolders in terms of contiguity statistics, as attested by a generally smaller number of genome fragments (i.e., scaffolds + unscaffolded contigs), the larger size of these fragments, as well as better contiguity indexes (N50, LG50 and LG75, Table 2). For instance, for both prokaryotes, WiseScaffolder was able to build a single scaffold covering more than 50 % of the whole genome (LG50 = 1), while for the H. sapiens Chr.14, this percentage was reached for 38 contigs with WiseScaffolder vs. 52, 74 and 460 for SCARPA, SSPACE and SOPRA, respectively. It is also noteworthy that SSPACE was also quite efficient on WH8103, while SCARPA proved the second best after WiseScaffolder for R. sphaeroides and H. sapiens Chr.14, according to contiguity indexes. Additional estimators provided by QUAST in contrast suggest that WiseScaffolder would result in more misassemblies than the other scaffolders. However, these estimators somewhat penalize WiseScaffolder because its purpose is not to assemble contigs at the sequence level like the other scaffolders. Instead, it generates an orientated map of contigs, in which the position and orientation of large contigs is unambiguous, but that of the small contigs in-between may be inaccurate due to the variability of MP insert size or the occurrence of collapsed repeats. This scaffolding strategy is highly secure, since the inter-contig regions comprising these small contigs (usually arisen from assembly bottlenecks) are only resolved after automatic scaffolding using contig extensions (Figs. 1 and 3), but it has for side effect to be interpreted by QUAST as relocation misassemblies (Table 2). Eventually, the global quality of the scaffolds produced by WiseScaffolder was also validated by the remarkable synteny of these scaffolds with that of the high quality reference genome of its close relative WH8102 (Figs. 2 and Additional file 1: Figure S1), with only three scaffolds covering most of the chromosome. By comparison, SSPACE and SOPRA performed almost as well in terms of synteny but with 1 and 5 additional scaffolds > 10 kbp, respectively, while SCARPA produced the most fragmented chromosome with only three scaffolds generated larger than 10 kbp, corresponding to only one fourth of the WH8102 genome. It must be noted that two of the three breakpoints common to all four assemblies correspond to the two identical copies of the ribosomal operon, whose size (~5.3 kb) exceeds the insert size of the MP library (~4 kb), whereas the third one corresponded to swmB, a gene coding for a giant protein (around 32 kb) involved in cell motility  that contains highly repetitive regions preventing a proper automatic assembly and scaffolding. The additional breakpoint observed in the SSPACE assembly compared to WiseScaffolder corresponds to two highly conserved hypothetical genes (orthologs of SYNW1563 and SYNW1565 in WH8102), both present in multiple copies in the two genomes. Many additional gaps were present in the assembly made with SCARPA and the absence of synteny of two of the three scaffolds with the WH8102 reference genome indicates the occurrence of chimerae (see Fig. 2d). Altogether, WiseScaffolder gave the best results on this dataset (Table 2 and Fig. 2) and allowed us to obtain a genome of much better quality than most currently published draft genomes. Furthermore, a key asset of WiseScaffolder compared to other scaffolders is that the ‘preprocess’ subcommand also provides very useful outputs for resolution of chimerae (Fig. 1) that, together with multiple copy areas, often constitute scaffolding bottlenecks. These outputs can then be used for further improvement of the quality of the genome assembly.
Semi-automatic improvement of the scaffolding and finishing of the Synechococcus sp. WH8103 genome
Post-scaffolding improvements of the genome assembly are generally achieved by ordering and merging scaffolds into a reduced set of gapped sequences and then closing the remaining gaps either by wet laboratory PCR amplification, followed by Sanger sequencing, or by computational approaches. For instance, tools such as ABACAS can be used to organize contig/scaffolds in a syntenic order with respect to a reference genome , then IMAGE or GapFiller to tentatively close gaps using paired reads [20, 21]. However, both approaches have limitations. Indeed, while wet laboratory experiments are generally costly and time consuming , most current computational algorithms despite being faster, only partially address the scaffolding and finishing issues.
Here, we describe a complete workflow for semi-automatic genome finishing dealing with most frequently encountered difficulties, such as closing remaining gaps, resolving collapsed repeats and correcting sequences of highly conserved multi-copy genes. For this purpose, the maps of oriented contigs, generated using the 'scaffold' sub-command, constitute a valuable tool for the manual scaffolding step (Fig. 1), by allowing one to easily manipulate contigs without immediately having to deal with their sequence information. In the case of WH8103, the manual improvement of this map using WiseScaffolder outputs allowed us to obtain a circular map of the complete genome without having to use a reference genome. Such scaffold maps have already been used with success in other genome projects aiming at getting complete genomes [23, 24].
Once the map was completed, a first series of gaps was closed by assembling the initial set of contigs together with local extensions of contig edges (Fig. 3). Assembly of these extensions benefits from using only a local selection of reads, which usually prevents de novo assembly issues associated with duplicated areas of the genome . Moreover, since the size of these extensions was most often close to the insert size of the MP library, many gaps were successfully solved this way. However, in the case of regions with low coverage and/or low complexity or when distance between two successive large contigs was larger than two MP insert size, this strategy only allowed us to partially fill the gap. This additional assembly step led to the generation of supercontigs, the contig composition of which was checked by comparison with the genome map, before being merged into a single, gapped circular genome (Fig. 1).
At this stage, all remaining gaps required a close visual inspection to be solved. Indeed, these gaps resulted either from tricky genome configurations (e.g., repeats at contig edges or in inter-contig regions), or from extremely low sequencing coverage, which may have led the CLC assembler to discard the corresponding reads at an early stage of the assembly. As in the strategy used by the IMAGE software , this step was performed using another round of iterative contig extensions but, in our case, extensions were made by retrieving then aligning reads matching a ~20 bp motif at the supercontig edges. This refining step allowed us to get a high quality ungapped genome sequence.
The final smoothing of the genome sequence consisted in the remapping of MPs (with a distance constraint) onto the genome in order to correct for possible coverage anomalies and for unresolved polymorphisms in highly conserved multi-copy genes , such as the psbA family, coding for the different D1 isoforms of photosystem II  that were initially assembled into a single consensus contig. This step also allowed us to get rid of the few residual issues, such as intra-contig chimera generated during the CLC assembly step (identified by coverage drops) or successions of close repeats collapsed into a single consensus sequence (identified by coverage rises; [27, 28]). In the case of WH8103, the sequence of the highly repetitive swmB gene , was manually reconstructed based on an estimation of the copy numbers for each repetitive motif. At last, this remapping step also allowed us to check that the read coverage was homogeneous along the final version of the genome.
WiseScaffolder is a novel scaffolder designed not only to produce high quality scaffolds, but also maps of oriented contigs, allowing the user to manually refine and eventually close the genome sequence. Using three datasets representative of both prokaryotic and eukaryotic genomes and of the current standard of the Illumina technology, the automatic part of this pipeline led to a very limited number of scaffolds and was found to perform better than the well-known scaffolders SSPACE and SOPRA and the most recent one SCARPA. The reliability of the scaffolds obtained for Synechococcus sp. WH8103 was confirmed by comparison with a closely related reference genome sequenced by Sanger technology . Here, we also propose guidelines for genome finishing that use the outputs generated by WiseScaffolder to refine the scaffolding. In our hands, this pipeline led to the complete closure of the WH8103 genome and was also successfully applied to 31 additional Synechococcus genomes, among which 28 were closed and only 1 to 3 gaps remained in the 3 incomplete, yet circularized genomes (http://application.sb-roscoff.fr/cyanorak/). Altogether, our results on both prokaryotes and eukaryotes genomes indicate that the automatic part of this pipeline should perform better than previous scaffolders for most genome projects using MPs, while the semi-automatic finishing part of the pipeline is applicable, with reasonable human cost, only when the assembly step results in a limited number of contigs.
It is worth noting that although the construction of MP libraries remains technically challenging, they constitute an undeniable asset for genome scaffolding and computational finishing and their use is therefore highly recommended for forthcoming projects aiming at getting complete genomes. Upcoming improvements in NGS technologies, including increase of read lengths, accuracy and length of MP insert sizes, which should ideally be larger than 6 kb in order to get over the ribosomal operon, should lead to even better performance of WiseScaffolder. Furthermore, even though the advent of single molecule real time sequencing is expected to further reduce the need for genome assembly, scaffolding and finishing, WiseScaffolder will remain valuable as long as the result of assemblers will not be a single circular chromosome. Finally, we anticipate that WiseScaffolder will also be a key asset to reconstruct uncultured genomes from complex environmental communities using MP read metagenomes, a current challenge in environmental genomics .
Materials and methods
Synechococcus sp. WH8103 (Roscoff Culture Collection strain: RCC2366), a clonal but non-axenic strain, was isolated by J. Waterbury in 1981 in the Northwestern Atlantic Ocean (28° 30' 0" N, 67° 23' 30" W). The genome sequencing dataset consists of two libraries sequenced by Illumina technology: a short insert PE library for genome assembly and a long insert MP library designed for genome scaffolding. Raw datasets are available via the Sequence Read Archive (SRA) under the EBI accession number ERP006796. The PE library was composed of 2 × 2.107 reads of 101 bp with an average insert size of 75 bp and the MP library of 2 × 4.1.107 reads of 101 bp with an average insert size of 4.2 kb (Table 1). In both cases, the coverage was around 800-fold. The closely related complete genome of Synechococcus sp. WH8102, previously sequenced using Sanger technology , was used as a reference to assess the quality of the scaffolding.
Two other datasets from the GAGE study , available at http://gage.cbcb.umd.edu/data/ and for which complete reference sequences are available, were used in this study to test the efficiency of WiseScaffolder with regard to other scaffolders. These include a second prokaryote, R. sphaeroides, as well as a representative eukaryotic genome, Homo sapiens Chr.14 (Table 1). In the case of R. sphaeroides, the dataset consists of an MP library of 2 × 106 reads of 101 bp with a 3,500 bp insert size and contigs generated using the Bambus2 assembler . For H. sapiens Chr.14, we used contigs assembled using CABOG (Celera Assembler with the Best Overlap Graph) and an MP library of 2.2 × 107 reads of 101 bp with a 2,280-2,800 bp insert size [14, 17].
Generating input data for WiseScaffolder
Three input files are necessary to run WiseScaffolder (Fig. 1): i) a series of contigs (multifasta file) generated by de novo assembly, ii) a ‘contig info table’ containing three columns specifying the contig identifiers as well as coverage and length of each contig, and iii) a ‘MP mapping table’ specifying the identifiers of MP reads, their contig best matches and their positions (5′- and 3′-ends) on contigs. A test data set including these three files and a handbook are available at http://abims.sb-roscoff.fr/wisescaffolder.
Generation of Synechococcus sp. WH8103 contigs
Initial assemblies of PE reads were realized de novo using the CLC AssemblyCell© 4.10 (CLC Inc, Aarhus, Denmark) with default parameters. In order to select only contigs corresponding to Synechococcus (and not to co-occurring heterotrophic bacterial contaminants), PE reads were re-mapped onto contigs using CLC mapper, then average coverage values for each contig were obtained using CLC assembly info. Based on the average coverage of Synechococcus contigs, a threshold value of 500 x was used.
Mapping of MP onto contigs
This task was realized using either MegaBLAST  or Bowtie2  with default parameters. MegaBLAST can generate tabulated text outputs, which are easy to manipulate by bash scripting. However, both pairs are mapped separately and resulting files then need to be joined to build the custom 7-column tabulated file, one of the two formats accepted by WiseScaffolder. Bowtie2 has the advantage to be much faster and parallelizable. By mapping both pairs simultaneously, it can generate a SAM (Sequence Alignment/Map)-formatted file , also directly compatible with WiseScaffolder. In both cases, only the most accurate hits were conserved (i.e., full length alignments with 0–3 mismatches).
Scaffolding steps using WiseScaffolder
This subcommand generates the configuration file, which will be used throughout the scaffolding pipeline. This file specifies several manually editable parameters, namely: i) default names for the main WiseScaffolder outputs, ii) the column indexes that need to be read from both tabulated input files (‘MP mapping table’ and ‘contigs info table’), iii) the upper limits of insert size distributions for both the main MP and small insert size populations (Fig. 4), the latter needing to be removed from MP links between contigs, iv) a bin size for contig length-based histograms, set by default at 50 bp, and v) the minimal size of big contigs, which is usually set at the upper limit of the insert size of the main MP population. If not known prior to running WiseScaffolder, the latter limits can be visually determined from the ‘MP insert size graph' (Fig. 4), which is generated by the WiseScaffolder 'preprocess' subcommand when used with the --dumpfile option (Additional file 1: Table S1). When the small insert size MP population is absent, the corresponding parameter must be set at 0.
The main goal of this subcommand is to detect chimerae located within ‘big’ contigs and to estimate the number of copies of each contig, as deduced from their assembly coverage. As a result, this preprocessing step generates two files: the ‘chimera resolution file’ and the ‘contig copy number file’, which can be further corrected by hand before being re-imported for the automatic scaffolding step (‘scaffold’ subcommand). Indeed, the latter step can be greatly affected by the presence of chimerae as well as multi-copy genes, which are often assembled into consensus contigs, the coverage of which is a multiple of that observed for single-copy chromosomal regions.
The initial ‘chimera resolution file’ is a 5-column table listing all contig identifiers and positions as well as the results of the automatic chimerae detection step (Additional file 1: Figure S2). In principle, a single-copy contig with a size exceeding the MP insert size should have no more than two other neighboring big contigs in the chromosome. Chimera suspicion warnings are raised when a large contig has a significant number of MP links with more than the expected two neighboring big contigs. These contigs are then tagged as potentially being chimeric in the ‘chimera resolution file’. The exact location of each chimera component can be determined by plotting the contig ‘linkage location graph’ for the chimera candidate (Additional file 1: Figure S3). The ‘chimera resolution file’ may then be manually modified by splitting the chimeric contig into two (or more) components with variable overlaps (Additional file 1: Figure S2).
The ‘contig copy number file’ provides an estimation of the number of copies of each contig. Based on the fact that the largest contig is likely to be single-copy, this number is calculated as the rounded ratio of the contig coverage to the coverage of the largest contig, both values being found in the’contigs info table’. This information is important since only single-copy contigs are considered for the first step of automatic scaffolding.
Additionally, the ‘preprocess’ subcommand also generates, using the option --dumpfiles (Additional file 1: Table S1), a number of outputs dedicated to the manual refinement of scaffolding and finishing, as illustrated in Fig. 5. These include i) a ‘MP insert size graph’ (see also Fig. 4), showing the distribution of the MP insert sizes, as determined using MP reads mapping on the same contig, ii) a ‘global link map’, i.e. a symmetric matrix providing for each contig the number of MP reads linking it to other contigs, iii) a ‘neighborhood link map’, similar to the ‘global link map’ but with an indication of the location of MP reads on the contig (5' or 3' ends) and their orientation with regard to the contig, and iv) a ‘linkage location graph’ per contig, used to draw a histogram of the number of links with all other contigs per range of position. Clean versions of both ‘global link map’ and ‘neighborhood link map’ are also generated after discarding noisy links, i.e., either short-insert MPs or those with an insert size more than 1.5-fold the upper limit of the main MP population (see Fig. 4).
This subcommand constitutes the automatic scaffolding step. It uses i) the ‘chimera resolution file’ to split chimerae and redistribute their corresponding MP links to the different chimera components, ii) the ‘contig copy number file’ that sets the number of copies of each contig, as well as iii) the ‘MP mapping table’ and iv) the ‘contigs info table’ in order to infer the links between the neighboring contigs, information used to organize contigs into scaffolds. For this purpose, two modules are run successively: the ‘iterative_scaffold_extender’ (ISE) and the ‘small_contig_inserter’ (SCI).
The ISE module focuses on ordering and orientating ‘big contigs’. The largest contig is used as a seed for a first round of scaffolding. Based on the links between the neighboring contigs, the ISE appends on both sides of the building scaffold, in priority large contigs, otherwise small single-copy contigs, starting with the largest one. This process iterates on both sides of the scaffold until no more big or small single-copy contig can be added. If some large contigs remain unscaffolded, a new scaffold starts with the largest one, and so on until all large contigs are scaffolded. Termination of scaffold extension is generally caused by the presence of multi-copy contigs (e.g., the ribosomal operon), which are excluded by the ISE module to avoid synteny ambiguities due to their occurrence at different locations in the genome.
Subsequently, the SCI module attempts to insert remaining small contigs (single- and multi-copy) within existing scaffolds. For each of these small contigs, their links with neighboring large contigs are analyzed to determine all possible insertion points within the scaffolds and only those congruent with the known succession of big contigs are retained. When multiple copy contigs are inserted at different locations, their copy number is mentioned in the resulting ‘scaffold maps file’. It is noteworthy that no small contigs are added at the edges of scaffolds and, as a consequence, no scaffolds are merged by the SCI module.
The ‘scaffold’ subcommand eventually generates a ‘scaffold maps file’ (see Additional file 1: Figure S4) that can further be manually improved based on the preprocessing outputs.
This subcommand builds the scaffolds as fasta files using the ‘scaffold maps file’ and ‘chimera resolution file’ as well as the ‘contigs multifasta file’ generated prior to scaffolding. Considering that the variability of the insert sizes within the MP library (±1 kb around the peak) does not allow to determine precisely the gap size between contigs and that the quality of the de novo assembly makes unlikely the occurrence of large gaps, this subcommand was set to arbitrarily add 50-Ns between contigs.
Manual improvement of scaffolds and finishing of Synechococcus sp. WH8103
Completion of the scaffold map
The first manual step after running WiseScaffolder consisted in ordering and orienting the 3 scaffolds to obtain a circular map of the whole chromosome of Synechococcus sp. WH8103. To do this, we used the ‘scaffold maps file’, which contains the list of contigs within each scaffold, and determined their neighborhoods using two outputs of WiseScaffolder, the ‘linkage location graphs’ and the ‘neighborhood link map’ (Figs. 1 and 5).
Local reassemblies and de novo scaffold assembly
In order to get the inter-contig sequences, we assembled paired reads complementary to those mapping at contig edges (Fig. 3). These new contigs covering inter-contig areas were assembled together with the initial contigs using Geneious v.R6 (Biomatters; http://www.geneious.com) and the consistency of the resulting supercontigs with the scaffold map was verified in terms of contig order. Additionally, sequence mismatches between new and initial contigs, often resulting from low quality extremities of new contigs, were manually corrected by trimming. The different supercontigs obtained using this strategy were then ordered according to the scaffold map and separated by 50-Ns gaps.
Manual gap closure
Remaining gaps were eventually closed by a second type of contig extensions, consisting in extracting then aligning reads (MP or PE) matching a ~20 bp motif at the very edge of the contig to be extended. Read alignments and integration of contig extensions into the gapped genome sequence were both made using Geneious and iterated until complete gap closure.
The next step consisted in remapping the MP reads onto the ungapped scaffold in order to determine the read coverage along the assembled genome. Indeed, the sequencing coverage is expected to be rather homogeneous, except in low complexity regions, which display a reduced coverage often due to the presence of homopolymers. Thus, local variations of the coverage might indicate previously undetected errors made during the de novo assembly step: coverage drops most often indicate the occurrence of intra-contig chimerae, while highly covered areas are generally observed for collapsed multi-copy genes or repeated domains. In the latter case, the true number of gene or domain copies may be estimated based on the coverage of this specific genomic region with respect to the rest of the genome. It is noteworthy that large, circularizable areas displaying a high coverage might also be due to mobile elements present in several copies with at least one integrated in the chromosome and the other(s) corresponding to independent plasmids.
The final step consisted in a global polymorphism correction based on mapping of MP reads onto the assembled genome. First, a weight-position matrix was built, giving at each position the number of A, C, T or G nucleotides found in the reads. The matrix was then analyzed either to correct a nucleotide (when more than 50 % of the reads displayed a different nucleotide than the assembled genome at this position) or to flag the positions when the nucleotide identity was ambiguous (i.e., when two nucleotides were equally abundant, no nucleotides had a frequency higher than 50 % or when the coverage at this position was too low). The script used to perform this step is available on the WiseScaffolder website.
The base numbering of the circularized sequence of Synechococcus sp. WH8103 was started 174 bp before dnaN, corresponding approximately to the origin of replication. It was then automatically annotated through the Manatee pipeline (Institute of Genome Sciences, Maryland, USA) and submitted to EBI under the accession number LN847356.1.
Performance and comparison with other scaffolders
The results obtained with WiseScaffolder were compared to that obtained with SSPACE (v2), SOPRA (v1.4.6) and SCARPA (v0.241). While the mapping of the MP library against the contigs is included in the scaffolding process of SSPACE, this step was performed using Bowtie2  with default parameters for SOPRA, SCARPA and WiseScaffolder. For all three datasets, insert sizes used as setting for scaffolding are indicated in Table 1. Additional file 1: Table S2 details the wall-clock running times and memory usage for the four tested scaffolders. Although WiseScaffolder tends to be slightly more memory and time consuming than its counterparts, the memory requirement remains perfectly compatible with current standard cluster capacity and the running time is only a matter of a few hours. Additionally, the Galaxy implementation publicly available at http://webtools.sb-roscoff.fr is associated with a cluster with 256 Gb of memory. Additional file 1: Figure S5 shows the evolution of memory usage and running time for the most demanding ‘preprocess’ subcommand applied to the 42 contigs of WH8103 for an increasing number of MP mappings. Altogether, these results emphasize the increasing amount of memory required as a function of both the numbers of contigs and mapping results imported during the ‘preprocess’ and ‘scaffold’ subcommands. As a consequence, it is recommended to run the application on a cluster with a fairly large amount of memory (~100 Gb). However, WiseScaffolder can also be run efficiently on a personal computer with a limited amount of RAM, with little impact on the resulting assembly, using a subset of MPs that map the different contigs with high accuracy (i.e., full length alignments with less than 4 mismatches). A script allowing to sub-sample MP mapping from a SAM file is available on the WiseScaffolder website.
Implementation and availability
Developed in Python with a few BioPython dependencies (essentially for the ‘buildfasta’ subcommand), WiseScaffolder is multi-platform and single-threaded. The code structure potentially allows the addition of scaffolding modules to the chain of actions. WiseScaffolder is open source and was installed on the local Galaxy instance of the ABiMS platform at http://webtools.sb-roscoff.fr. The application, the Galaxy wrapper, a handbook, test files and various peripheral scripts are available at http://abims.sb-roscoff.fr/wisescaffolder.
Next Generation Sequencing
iterative scaffold extender
small contig inserter
Scholz MB, Lo CC, Chain PS. Next generation sequencing and bioinformatic bottlenecks: the current state of metagenomic data analysis. Curr Opin Biotechnol. 2012;23(1):9–15.
Barbosa EG, Aburjaile FF, Ramos RT, Carneiro AR, Le Loir Y, Baumbach J, et al. Value of a newly sequenced bacterial genome. World J Biol Chem. 2014;5(2):161–8.
Zerbino DR, Birney E. Velvet: algorithms for de novo short read assembly using de Bruijn graphs. Genome Res. 2008;18(5):821–9.
Zerbino DR, McEwen GK, Margulies EH, Birney E. Pebble and rock band: heuristic resolution of repeats and scaffolding in the velvet short-read de novo assembler. PloS one. 2009;4(12):e8407.
Rodrigue S, Materna AC, Timberlake SC, Blackburn MC, Malmstrom RR, Alm EJ, et al. Unlocking short read sequencing for metagenomics. PloS one. 2010;5(7):e11840.
Peng Z, Zhao Z, Nath N, Froula JL, Clum A, Zhang T, et al. Generation of long insert pairs using a Cre-LoxP Inverse PCR approach. PloS one. 2012;7(1):e29437.
Leggett RM, Clavijo BJ, Clissold L, Clark MD, Caccamo M. NextClip: an analysis and read preparation tool for Nextera Long Mate Pair libraries. Bioinformatics. 2014;30(4):566–8.
Pop M, Kosack DS, Salzberg SL. Hierarchical scaffolding with Bambus. Genome Res. 2004;14(1):149–59.
Boetzer M, Henkel CV, Jansen HJ, Butler D, Pirovano W. Scaffolding pre-assembled contigs using SSPACE. Bioinformatics. 2011;27(4):578–9.
Dayarian A, Michael TP, Sengupta AM. SOPRA: Scaffolding algorithm for paired reads via statistical optimization. BMC Bioinformatics. 2010;11:345.
Salmela L, Makinen V, Valimaki N, Ylinen J, Ukkonen E. Fast scaffolding with small independent mixed integer programs. Bioinformatics. 2011;27(23):3259–65.
Donmez N, Brudno M. SCARPA: scaffolding reads with practical algorithms. Bioinformatics. 2013;29(4):428–34.
Hunt M, Newbold C, Berriman M, Otto TD. A comprehensive evaluation of assembly scaffolding tools. Genome Biol. 2014;15(3):R42.
Salzberg SL, Phillippy AM, Zimin A, Puiu D, Magoc T, Koren S, et al. GAGE: A critical evaluation of genome assemblies and assembly algorithms. Genome Res. 2012;22(3):557–67.
Gurevich A, Saveliev V, Vyahhi N, Tesler G. QUAST: quality assessment tool for genome assemblies. Bioinformatics. 2013;29(8):1072–5.
Koren S, Treangen TJ, Pop M. Bambus 2: scaffolding metagenomes. Bioinformatics. 2011;27(21):2964–71.
Miller JR, Delcher AL, Koren S, Venter E, Walenz BP, Brownley A, et al. Aggressive assembly of pyrosequencing reads with mates. Bioinformatics. 2008;24(24):2818–24.
McCarren J, Brahamsha B. SwmB, a 1.12-megadalton protein that is required for nonflagellar swimming motility in Synechococcus. J Bacteriol. 2007;189(3):1158–62.
Assefa S, Keane TM, Otto TD, Newbold C, Berriman M. ABACAS: algorithm-based automatic contiguation of assembled sequences. Bioinformatics. 2009;25(15):1968–9.
Tsai IJ, Otto TD, Berriman M. Improving draft assemblies by iterative mapping and assembly of short reads to eliminate gaps. Genome Biol. 2010;11(4):R41.
Boetzer M, Pirovano W. Toward almost closed genomes with GapFiller. Genome Biol. 2012;13(6):R56.
Nagarajan N, Cook C, Di Bonaventura M, Ge H, Richards A, Bishop-Lilly KA, et al. Finishing genomes with limited resources: lessons from an ensemble of microbial genomes. BMC Genomics. 2010;11:242.
Barton MD, Barton HA. Scaffolder - software for manual genome scaffolding. Source Code Biol Med. 2012;7(1):4.
Barton MD, Barton HA. Genomer--a Swiss army knife for genome scaffolding. PloS one. 2013;8(6):e66922.
Otto TD, Sanders M, Berriman M, Newbold C. Iterative Correction of Reference Nucleotides (iCORN) using second generation sequencing technology. Bioinformatics. 2010;26(14):1704–7.
Garczarek L, Dufresne A, Blot N, Cockshutt AM, Peyrat A, Campbell DA, et al. Function and evolution of the psbA gene family in marine Synechococcus: Synechococcus sp. WH7803 as a case study. Isme J. 2008;2(9):937–53.
Mulyukov Z, Pevzner PA: EULER-PCR: finishing experiments for repeat resolution. Pac Symp Biocomput 2002:199–210.
Koren S, Miller JR, Walenz BP, Sutton G: An algorithm for automated closure during assembly. Bmc Bioinformatics 2010, 11.
Palenik B, Brahamsha B, Larimer FW, Land M, Hauser L, Chain P, et al. The genome of a motile marine Synechococcus. Nature. 2003;424(6952):1037–42.
Iverson V, Morris RM, Frazar CD, Berthiaume CT, Morales RL, Armbrust EV. Untangling genomes from metagenomes: revealing an uncultured class of marine Euryarchaeota. Science (New York NY). 2012;335(6068):587–90.
McGinnis S, Madden TL: BLAST: at the core of a powerful and diverse set of sequence analysis tools. Nucleic Acids Res 2004, 32(Web Server issue):W20-25.
Langmead B, Salzberg SL. Fast gapped-read alignment with Bowtie 2. Nat Methods. 2012;9(4):357–9.
Li H, Handsaker B, Wysoker A, Fennell T, Ruan J, Homer N, et al. The Sequence Alignment/Map format and SAMtools. Bioinformatics. 2009;25(16):2078–9.
Delcher AL, Salzberg SL, Phillippy AM: Using MUMmer to identify similar regions in large sequence sets. Curr Protoc Bioinformatics 2003, Chapter 10:Unit 10 13.
This work was supported by the French “Agence Nationale de la Recherche” BioAdapt Program (SAMOSA, ANR-13-ADAP-0010), the European Union’s Seventh Framework Programmes FP7 MicroB3 (grant agreement 287589; http://www.microb3.eu) and MaCuMBA (grant agreement 311975, http://www.macumbaproject.eu). We thank the Genoscope, particularly Karine Labadie, Jean-Marc Aury and Patrick Wincker, for whole genome sequencing of Synechococcus sp. WH8103 in the framework of the METASYN project (http://www.genoscope.cns.fr/spip/Variety-of-photosynthetic-pigments.html). We warmly thank Florian Humily and Morgane Ratin for strain purification and DNA extraction, the Roscoff Culture Collection for maintaining the Synechococcus strain used in this study as well as Christophe Caron for his active support all along the project.
The authors declare that they have no competing interests.
GKF, LG and FP conceived the study and wrote the paper, MH and GKF developed the software, GA developed the Galaxy wrapper and EC contributed ideas and tools for the analysis. All authors read and approved the final manuscript.
Parameters to be used with the different WiseScaffolder subcommands. Table S2. Wall-clock running times and memory usage for the four scaffolders used in this study. Figure S1. Whole genome alignments of Synechococcus spp. WH8103 and WH8102. Figure S2. Example of a ‘chimerare solution file’ before and after resolution of a chimeric contig. Figure S3. Schematic representation of the linkage location graph for the chimeric contig_1, consisting in two chimera components sharing a common sequence. Figure S4. Description of the scaffolds as generated by the scaffold subcommand and after reconstruction of the genome map. Figure S5. Performances of WiseScaffolder preprocess subcommand with Synechococcus sp. WH8103. (PDF 587 kb)