How accurately is ncRNA aligned within whole-genome multiple alignments?
BMC Bioinformatics volume 8, Article number: 417 (2007)
Multiple alignment of homologous DNA sequences is of great interest to biologists since it provides a window into evolutionary processes. At present, the accuracy of whole-genome multiple alignments, particularly in noncoding regions, has not been thoroughly evaluated.
We evaluate the alignment accuracy of certain noncoding regions using noncoding RNA alignments from Rfam as a reference. We inspect the MULTIZ 17-vertebrate alignment from the UCSC Genome Browser for all the human sequences in the Rfam seed alignments. In particular, we find 638 instances of chimeric and partial alignments to human noncoding RNA elements, of which at least 225 can be improved by straightforward means. As a byproduct of our procedure, we predict many novel instances of known ncRNA families that are suggested by the alignment.
MULTIZ does a fairly accurate job of aligning these genomes in these difficult regions. However, our experiments indicate that better alignments exist in some regions.
In this time when so many genome sequences are reaching completion, alignments of multiple whole genomes are of great value to biologists, since enlightening evolutionary information is encoded in the conservation and variation across species. Multiple alignment on genomic scales is also a great challenge to algorithm designers. Protein-coding regions usually evolve more slowly than noncoding regions, and therefore tend to be easier to align. In contrast, noncoding regions are still challenging to align correctly. Because of this, a number of recent reviews and articles [1–4] have made compelling pleas for methods to assess the accuracy of multiple sequence alignments and to compare the alignments produced by different tools.
We use alignments of noncoding RNA (ncRNA) as a test of the accuracy of multiple alignment of genomic regions that are difficult to align. This is a rather challenging test, as many functional RNAs exhibit weak primary sequence conservation . As a byproduct of our procedure, we predict many novel instances of known ncRNA families that are suggested by the alignment. We return to this topic in the Discussion section.
Evaluating the accuracy of multiple sequence alignments
Multiple sequence alignment is a difficult computational problem. Technically, the problem of finding an optimal multiple sequence alignment is NP-complete . In practice, what this means is that finding an optimal multiple sequence alignment requires computation time that grows exponentially with the number of sequences to be aligned, making it impractical for aligning more than a few sequences. Note that this is true even if the sequences are relatively short; aligning multiple genome-size sequences adds another level of complexity.
Because of this inherent difficulty, algorithm designers are forced to invent heuristic methods that produce results that can only approximate the optimal multiple sequence alignment. Many such alignment tools have been proposed over the past 20 years. Since they employ various heuristics intended to approximate an optimal solution, any two such methods often produce incomparable results when aligning the same set of input sequences. This situation naturally raises the questions of (1) assessing the quality of resulting multiple alignments and (2) deciding which of several multiple alignments produced by different tools is "best".
The situation becomes even worse when we consider whole-genome multiple alignments. This is due to the multitude of genomic rearrangements (inversions, translocations, duplications, chromosome fusions and fissions, etc.) that occur over the course of evolution . The traditional alignment problem is not defined to deal with such "nonlinear" events. In what follows, we will categorize methods that have been proposed for assessing the accuracy of traditional multiple sequence alignments (where much work has been done), and highlight those that have been applied to assess the accuracy of whole-genome multiple alignments (where relatively little has been done to date).
One approach to measuring the accuracy of multiple sequence alignments is to use artificial sequences resulting from a simulation of evolutionary processes [8–11]. Since the experimenter can track all evolutionary events, identifying the truly homologous characters is straightforward. These known homologies can be used to measure the accuracy of any alignment to be tested. This approach has also been employed to evaluate genome-size multiple alignments by Blanchette et al.  and by Prakash and Tompa . An obvious drawback of this simulation approach is its sensitivity to assumptions about the underlying evolutionary processes, which are not at all well understood.
Another approach is to run the alignment program on a set of sequences in which certain features are known a priori to be homologous, and measure the accuracy with which these known homologous features are aligned. This approach was used in genome-size alignment studies by Brudno et al.  and by Margulies et al. . The most obvious choice for the known homologous features is a set of coding exons. However, this choice suffers from the shortcoming that such features are usually well conserved and easy to align, and most algorithms do so quite accurately. In addition to using coding exons, Margulies et al.  also tested alignment accuracy using ancestral repeats, which tend to be more challenging to align correctly than coding exons. For this general approach, though, many known sets of homologous sequences have been discovered using some alignment algorithm, which leads to circularity if then used to test the accuracy of an alignment algorithm. In addition, no accuracy information is provided for aligned regions other than the previously known orthologous features.
A number of papers have suggested methods that inspect multiple sequence alignments, judging regions of the alignment that show good conservation across the aligned sequences to be well aligned, and even removing sequences from the alignment that show lack of good conservation [15–18]. While good conservation often implies good alignment, the converse need not be true. In fact, in our case of interest, the alignment of homologous RNA elements, it is well known that sequence conservation may be very low if instead the RNA secondary structure conservation is strong .
Lassmann and Sonnhammer  proposed a measure to assess alignment quality by comparing several multiple sequence alignments, assuming that regions identically aligned by multiple tools are more reliable than regions differently aligned. This method requires several auxiliary alignments in order to evaluate the alignment of interest. In the same general class are methods that employ other auxiliary information, such as protein secondary structure, in order to assess alignment quality .
A final approach is one designed to provide a statistical assessment of the accuracy of a given multiple sequence alignment, by extending the theory of Karlin and Altschul  from pairwise to multiple alignments. This was done for short multiple alignments by Prakash and Tompa , and later extended by them to measure the alignment quality of all portions of a genome-size multiple sequence alignment . In the latter paper the authors found approximately 10% of the UCSC Genome Browser's human chromosome 1 alignment to be suspiciously aligned. This is a portion of the same whole-genome alignment we analyze in this paper.
RNA families as a test of accuracy
The approach we take falls into the second category listed above. Instead of using well conserved coding regions as the homologous test features, however, we use curated alignments of noncoding RNA (ncRNA) from Rfam (version 7.0, March 2005). Rfam is a collection of ncRNA families that contains multiple sequence alignments and covariance models of these families [24, 25].
As an illustration, Figure 1 shows Rfam's seed alignment and the predicted secondary structure of the Iron Response Element family (RF00037). Most functional RNAs tend to maintain their base-paired structure over conservation of primary sequence . To illustrate this, in Figure 1, the primary sequences of the 10th element (Gal.gal. X13753.1/830-856) and the 11th element (Gal.gal. M16343.1/1306-1335) are different. For example, the 10th element has a U in the first position, and an A in the last position, while the 11th element has a G and a C respectively. However, this does not disrupt the similarity of their predicted secondary structures, because both UA and GC form Watson-Crick base pairs.
The seed alignment of each Rfam family is hand-curated by human experts, based on both the secondary structure and primary sequence of trusted example RNAs. Using the Infernal software package , the seed alignment is used to train a covariance model [24, 25], a statistical model akin to a hidden Markov model. Together with a score threshold also chosen by the Rfam curators, these models are then used to search genomic DNA for additional instances of the specific RNA family represented by the seed alignment, automatically producing Rfam's so-called full alignments. We use Rfam's covariance model and score threshold as the definitive rule for membership in ncRNA families and for alignment. Rfam and Infernal are considered by experts to be the most accurate general tools for defining membership in ncRNA families and for alignment of family members. There are several databases of recognized ncRNAs of various types but, to the best of our knowledge, only Rfam/Infernal provides both expert-curated alignments and a simple automated search tool leveraging those alignments.
Multiple sequence alignments considering the secondary structure such as Rfam's covariance models are more reliable than alignment tools that only consider primary sequences. This makes these seed alignments a challenging test case for any whole-genome multiple alignment that is based on primary sequence alone. We apply this challenging test to the 17-vertebrate whole-genome alignment produced by MULTIZ  and available on the UCSC Genome Browser . Although MULTIZ is most frequently shown to be quite accurate in these challenging cases, our study does reveal occasional compelling evidence of misalignment. Two of the more interesting categories are summarized here:
For 5.4% of the nonhuman sequences aligned to some human ncRNA, what is aligned to the human ncRNA is not a contiguous sequence. Instead, it is composed of sequence fragments from different regions or even different chromosomes, none of these fragments individually passing Infernal's test of ncRNA family membership. We call these "chimeric alignments". For 45% of these chimeric alignments, one of the aligned fragments can be extended in its native genomic context to reveal a full ncRNA family member that is probably the correct alignable ortholog. These improvable chimeric alignments are compelling instances of misalignment.
For 5.1% of the nonhuman sequences aligned to some human ncRNA, what is aligned includes a large gap in the nonhuman species, and the aligned fragment by itself again does not pass Infernal's threshold for ncRNA family membership. We call these "partial alignments". For 26% of these partial alignments, the fragment can be extended in its native genomic context to reveal a full ncRNA family member that is probably the correct alignable ortholog. These improvable partial alignments are compelling cases of false negative orthology predictions by the alignment algorithm.
RNA prediction from reliable alignments
Two groups have developed RNA prediction tools using comparative genomics methods [28, 29]. The MULTIZ whole-genome alignment of 8 vertebrate species was used, and the segments with low phastCons  sequence conservation scores and segments with too few species were removed. This filtering process leaves a set of conserved segments spanning less than 5% of the reference human genome. Based on the conserved segments, they evaluated structural conservation of base-pairing patterns and identified tens of thousands of candidate functional RNA elements. Our goal is opposite to the goal of these groups. They assumed the MULTIZ multiple sequence alignment to be reliable, and used that to predict ncRNAs. We assume that known ncRNA covariance models provide reliable alignments, and use them to evaluate the accuracy of the MULTIZ multiple alignments in those difficult noncoding regions. Torarinsson et al.  discovered many conserved RNA structures in regions that MULTIZ did not align at all, but are presumably syntenic.
UCSC genome browser and MULTIZ
The UCSC Genome Browser is a powerful web tool that provides the reference sequence and working draft assemblies for a large collection of genomes . It is a multifaceted and reliable display of any requested portion of genomes at any scale, as well as many annotation tracks, including assembly contigs and gaps, mRNA and expressed sequence tag alignments, multiple gene predictions, cross-species homologies, single nucleotide polymorphisms, sequence-tagged sites, radiation hybrid data, transposon repeats, and more as a stack of coregistered tracks.
The 17-vertebrate whole-genome alignment that we evaluate is taken from the UCSC Genome Browser database. The 17 vertebrates of the alignment are human (hg), chimp (panTro), rhesus monkey (rheMac), rat (rn), mouse (mm), rabbit (oryCun), cow (bosTau), dog (canFam), armadillo (dasNov), elephant (loxAfr), tenrec (echTel), opossum (monDom), chicken (galGal), frog (xenTro), tetraodon (tetnig), fugu (fr), and zebrafish (danRer). Some species have not been fully sequenced or have low sequence coverage. The 17-vertebrate whole-genome alignment (to human genome assembly NCBI Build 36.1, UCSC hg18, March 2006) is an update and expansion of the older 8-vertebrate alignment. It was produced by a computational pipeline including BLASTZ , chaining and netting , and MULTIZ . For the remainder of this paper, we will refer to this computational pipeline simply as "MULTIZ". MULTIZ uses the progressive alignment technique to align multiple sequences, including highly rearranged or incomplete sequences.
We first extract all the human sequences in the seed alignments from the Rfam database [24, 25]. These sequences are then uploaded to the UCSC genome browser  to find the chromosome number, strand, and start and end positions of the sequences in the human genome using the sequence alignment tool BLAT . After we get the precise locations of the sequences in the human genome, we retrieve MULTIZ multiple alignment files with each human Rfam sequence as the reference sequence.
We use the software package Infernal (version 0.7) to analyze each of the sequences aligned by MULTIZ to the human ncRNA. Infernal uses covariance models for sequence analysis of ncRNA families . For each ncRNA family, a covariance model based on the seed alignment and a threshold score are provided by Rfam. The seed alignment and threshold are curated by experts. Any sequence for which Infernal assigns a covariance model score above the threshold is classified as a member of that family. If a sequence aligned by MULTIZ to the human ncRNA element returns a score above the threshold, we conclude that this alignment is supported by Rfam. Otherwise, we search the nearby region of the MULTIZ alignment to look for a family member. The search space is bounded by 5 Kb on each side of the human element or the distance to the nearest human exon on each side, whichever is less. The motivation for this search is that, if a local misalignment has occurred, the orthologous ncRNA family member may be in the neighborhood of its aligned family members. We detect such an orthologous family member by using Infernal to search the neighborhood for any segment with a score above the threshold provided by Rfam. We find the bound of 5 Kb to be sufficiently liberal: of all the family members found within a 5 Kb neighborhood, 90% are within 10 bp of the nearest human family member, and only 8 instances (1%) are more than 100 bp from the nearest human family member. Figure 2 is an overview of this first phase of the evaluation process. The first phase evaluation is done on all seed alignments in Rfam, and the results are summarized in Table 1. We extract 585 human elements from 201 ncRNA families. Of these, 172 human elements are perfectly aligned with members of the same RNA family in every aligned species (see Figure 3). These are labeled "perfect alignments" in Table 1. The remaining 413 imperfect alignments have at least one aligned sequence receiving poor covariance model score, and require a neighborhood search to the nearest human exons or the 5 Kb boundary. These are not necessarily misalignments: many may indicate loss of an ncRNA in some species.
We find 424 human ncRNAs in the neighborhood searches of the 413 imperfect alignments. The 11 additional human ncRNAs are elements not included in the seed alignments, but identified by Infernal to be members of the same ncRNA family. There are 6043 segments in other species aligned to human ncRNAs, including the perfect alignments in Table 1. Table 2 categorizes these as follows:
4025 RNA family members in other species are perfectly aligned to human ncRNAs; that is, the segment aligned to the human ncRNA is assigned a high covariance model score without any neighborhood search. The rest of the aligned segments receive low covariance model score.
For 707 segments, an Rfam member that is not perfectly aligned to other human ncRNAs in the family can be found in the neighborhood search. These are labeled as shifted elements in Table 2. Figure 4 illustrates a case of a particularly large shift in an alignment of a human SNORD113 (C/D box small nucleolar RNA SNORD113/SNORD114, RF00181) on chromosome 14. An RNA element in elephant (loxAfr1.scaffold 44287) is divided into halves by the alignment, each half aligned to a different human ncRNA. The two human ncRNAs are 1556 bp apart. Most of the 707 shifts are very small compared to this example.
For some species, the portion aligned to a single human ncRNA is not a contiguous sequence. Instead, it is composed of sequence fragments from different regions or even different chromosomes. These 328 discontiguous segments are labeled as chimeric alignments in Table 2. Figure 5 illustrates two examples of chimeric alignments of a human SNORA25 (small nucleolar RNA SNORA25, RF00402) on chromosome 7. Two sequences from different regions (dasNov1.scaffold 192792 and dasNov1.scaffold 7495) in armadillo are concatenated and aligned to a single human ncRNA. Also, two fragments from different chromosomes in mouse (mm8.chr13 and mm8.chr6) are aligned to the single human ncRNA.
Some of the segments receive low score because that species is only partially aligned to the human ncRNA. We find 310 such partial alignments. In this case, the segment might be a family member if the sequence were fully aligned in that region. Figure 6 illustrates partial alignments of a human SNORA42 (small nucleolar RNA SNORA42, RF00406) on chromosome 14. The segments in rabbit (oryCun1.scaffold 201547), tenrec (echTel1.scaffold 205400) and elephant (loxAfr1.scaffold 38492) appear to be partially aligned to the human ncRNA.
4 segments appear to be possible alignment inversions: a family member is identified on the other strand, but otherwise perfectly aligned to the human family member. These are all tRNAs in opossum. Since the number is so small, we will omit this category from the remaining discussion.
669 low score segments, fully aligned and contiguous, do not reveal a family member in the neighborhood search regions. These may well indicate actual loss of an ncRNA in that species rather than misalignment. Note that this case does not include the many instances when a species is completely absent from the alignment to the human ncRNA.
We perform a second phase of evaluation of each partial alignment. For each of the 310 partial alignments that receives a low covariance model score, we extract from its genome the original aligned segment plus 200 bp upstream and 200 bp downstream. (Note that this contextual sequence may not even be aligned by MULTIZ.) We use Infernal to search for a family member in this contiguous 400+ bp sequence that includes the fragment MULTIZ had aligned to the human ncRNA. In 79 of the 310 cases, we succeed in finding such a family member. As an example, in Figure 6, the segments in rabbit (oryCun1.scaffold 201547), tenrec (echTel1.scaffold 205400) and elephant (loxAfr1.scaffold 38492) all receive scores above the threshold of this family if extended.
A similar process is applied to each of the 328 chimeric alignments we find in the first phase of evaluation. We extract from its genome the chimeric fragments aligned to human ncRNAs, plus 200 bp upstream and 200 bp downstream of each fragment. This results in at least two 400+ bp sequences. In total, we find that family members could be restored in 146 of the 328 chimeric alignments by this simple process. For example, in Figure 5, for the species armadillo, when we extract a longer sequence from the genome at the position of the first fragment, dasNov1.scaffold 192792, this fragment extends to become a family member. For mouse, the extended sequence of the fragment in mm8.chr13 is also a member in the family.
We next categorize the aligned segments of Table 2 by species. The results are shown in Figure 7. For each species, the bars show the percent of aligned segments for that species in each of the five categories of Table 2 (omitting inversions because of the small number). The number next to the species name is the number of alignments in which that species is included.
MULTIZ does a fairly accurate job of aligning the vertebrate genomes in the ncRNA regions, particularly given the challenging nature of correctly aligning these elements. 66.6% of the elements aligned by MULTIZ to human ncRNA have a high covariance model score. These are very likely to be true positives of the alignment method. Conversely, only the large shifts, the 328 chimeric alignments, and the 79 improvable partial alignments are strong candidates as false positives and false negatives of the alignment method. These total approximately 7% of the elements aligned by MULTIZ to human ncRNA. Our results also suggest ways to improve some of the imperfect alignments.
Our results are roughly consistent with those of Prakash and Tompa , who used entirely different methods to assess whole-genome alignment accuracy, based on the statistical theory of Karlin and Altschul . Like us, they found that MULTIZ generally was quite accurate at aligning orthologous sequences, but they also identified approximately 10% of MULTIZ's human chromosome 1 alignment to be suspiciously aligned.
Comparing our findings to those of Brudno et al.  on the 1 Mb CFTR region, their multiple alignment tool MLAGAN perfectly aligned at least 94% of the human coding exons to the orthologous exons in each of 8 other mammalian genomes. This gives support to the belief that ncRNA elements are more difficult targets for accurate multiple alignment than coding exons are. Margulies et al.  performed similar experiments on the ENCODE regions, but reported much lower accuracy in aligning coding exons for the four multiple alignment algorithms they tested, TBA, MLAGAN, MAVID, and PECAN. Possible explanations for their lower accuracy include the following:
The CFTR region is nicely syntenic, with few duplications, in the aligned species, whereas most of the ENCODE regions are not as well conserved.
The quality of exon annotation in the ENCODE regions was not as high as that in the CFTR region, which has received more attention.
Some species had not yet been sequenced in a particular ENCODE region, or its sequence was not chosen in ENCODE's orthology prediction phase.
The MLAGAN alignment of the CFTR region was of 12 species, whereas the ENCODE alignments were of 28 species, which is more challenging.
If the procedures we described for testing ncRNA alignment accuracy were to be repeated for whole-genome alignments produced by other tools such as MLAGAN, MAVID, and PECAN, we predict that the results would be comparable to what we reported in Table 2 and Figure 7. We do not believe any of our results to be peculiar to MULTIZ. Instead, we believe that they illustrate an inherent difficulty in aligning ncRNA for any alignment method that relies on primary sequence alone. However, Margulies et al.  reported a surprising level of discrepancy among the four alignments they tested, with MAVID generally demonstrating somewhat lower sensitivity and specificity than that of the other methods, so we would certainly expect some similar amount of variance in the accuracy of ncRNA alignment.
Our assessment of alignment accuracy is only as good as Infernal's predictions. If the covariance model is inaccurate in certain instances, our assessment may be inaccurate as well. However, since the covariance model incorporates secondary structure, we trust that it is a reliable guide to the correct alignment of ncRNA.
In 11.7% of the aligned segments that we inspect, we find that the nearest family member in the other species is shifted from the human element. Most of these shifts seem rather small, and so represent minor misalignment or may not represent misalignment at all. For instance, 90% of these 707 shifted elements have both ends within 10 bp of the aligned human family member. It is worth noting, however, that even small misalignments may have adverse effects on some downstream analyses.
Our experiments reveal that in 5.4% of the cases, MULTIZ aligns discontiguous fragments to one human ncRNA, and it is likely to be quite misleading to draw any biological inferences from such chimeric alignments. Further analysis suggests that 44.5% of the chimeric alignments could be improved to family members by extending one of the fragments and aligning the extended piece to the human element. These improvable chimeric alignments are compelling instances of misalignment.
We also observe 5.1% of the cases to be partial alignments. These partial alignments fail to reveal a complete aligned RNA element. 25.5% of these partial alignments can be improved to family members by extending the aligned fragment. These improvable partial alignments are compelling cases of false negative orthology predictions by the alignment algorithm.
Washietl et al.  and Pedersen et al.  both use the MULTIZ whole-genome alignment to predict RNA secondary structures. The accuracy of their tools largely depends on the accuracy of the multiple alignment. Their results may be subject to false negative predictions due to various types of misalignments described above. Focusing on the highly conserved regions identified by the phastCons method, as they did, may have reduced the incidence of these misalignments since the regions where MULTIZ is likely to align imperfectly are often regions that are not highly conserved. On the other hand, such a strict selection likely causes them to miss many interesting candidates  while providing incomplete protection against alignment errors: phastCons was never intended as a method for measuring alignment correctness. Indeed, its purpose is to measure conservation, assuming that the alignment correctly aligns orthologous sites. Prakash and Tompa  have shown that misalignment of one sequence can often be found even in regions where phastCons scores are very high due to strong conservation in the remaining sequences.
There are 11.1% of the alignments that receive low covariance model score, but we do not find any better candidate in the neighborhood of the alignment. We do not have enough evidence to classify this type of alignment. It could be caused by loss of ncRNA element in that species, failure of the covariance model (e.g., an excessively restrictive family model or score threshold), or misalignment by MULTIZ.
Looking at Figure 7, there are some fairly clear trends in the alignments as we move farther from human in the phylogeny. The primates, not surprisingly, are extremely well aligned to human. The remaining mammals have a very similar breakdown to each other according to the five categories of alignment (with the possible exception of opossum, which looks more like chicken). Somewhat surprisingly, there seem to be no qualitative differences distinguishing the low-coverage assemblies rabbit, armadillo, elephant, and tenrec from the other nonprimate mammals. The remaining, more distantly related vertebrates show a decrease in the percent of perfectly aligned segments and a commensurate increase in the percent of partial alignments and possible losses of ncRNA as we move farther from human.
Many of the vertebrate instances of ncRNA elements discovered by our procedure are not included in Rfam. In theory, the Rfam staff could find all these instances (and many more) by running Infernal on each of the vertebrate genomes individually, ignoring alignment. However, it currently requires approximately one month using 1000 computers to approximate this Infernal search on their 8 Gb database. It is clearly impractical to extend this to all 17 sequenced vertebrates, and the gap is rapidly widening because of newly sequenced genomes. As an alternative, we propose using whole-genome alignment and lists of human ncRNAs from Rfam, restricting Infernal's search for family members to the sequences aligned to the human ncRNAs and their immediate neighborhoods. Although not exhaustive, our procedure provides an efficient and effective method for predicting ncRNA family members in newly sequenced genomes. By using whole-genome alignments in conjunction with Infernal as described, we exploit orthology and synteny with two good effects: (1) the search is made efficient by limiting it to the most promising regions suggested by the alignment and (2) the alignment adds extra evidence to Infernal's predictions, likely decreasing the incidence of false positives.
All alignments and Infernal results are available for viewing  using GMAJ , which was used to produce the images in Figures 3, 4, 5, 6. GMAJ is a tool for viewing and manipulating multiple sequence alignments. It offers a coloring feature for both the interactive graphical and text representation of the alignments. We use this feature to color all ncRNA elements, as well as the regions aligned to human ncRNA elements. The regions with a covariance model score above and within ten bits of the threshold are colored pink. Regions that receive a covariance model score above the threshold plus ten bits are colored red. Regions with a covariance model score below and within ten bits of the threshold are colored dark gray. Regions with a covariance model score below the threshold minus 10 bits but above 0 are colored light gray. The first row displays tick marks corresponding to the positions in the human reference sequence.
Batzoglou S: The many faces of sequence alignment. Briefings in Bioinformatics 2005, 6: 6–22. 10.1093/bib/6.1.6
Kumar S, Filipski A: Multiple sequence alignment: in pursuit of homologous DNA positions. Genome Res 2007, 17: 127–135. 10.1101/gr.5232407
Margulies EH, Cooper GM, Asimenos G, Thomas DJ, Dewey CN, Siepel A, Birney E, Keefe D, Schwartz AS, Hou M, Taylor J, Nikolaev S, Montoya-Burgos JI, Löytynoja A, Whelan S, Pardi F, Massingham T, Brown JB, Bickel P, Holmes I, Mullikin JC, Ureta-Vidal A, Paten B, Stone EA, Rosenbloom KR, Kent WJ, Bouffard GG, Guan X, Hansen NF, Idol JR, Maduro VV, Maskeri B, McDowell JC, Park M, Thomas PJ, Young AC, Blakesley RW, Muzny DM, Sodergren E, Wheeler DA, Worley KC, Jiang H, Weinstock GM, Gibbs RA, Graves T, Fulton R, Mardis ER, Wilson RK, Clamp M, Cuff J, Gnerre S, Jaffie DB, Chang JL, Lindblad-Toh K, Lander ES, Hinrichs A, Trumbower H, Clawson H, Zweig A, Kuhn RM, Barber G, Harte R, Karolchik D, Field MA, Moore RA, Matthewson CA, Schein JE, Marra MA, Antonarakis SE, Batzoglou S, Goldman N, Hardison R, Haussler D, Miller W, Pachter L, Green ED, Sidow A: Analyses of deep mammalian sequence alignments and constraint predictions for 1% of the human genome. Genome Res 2007, 17: 760–774. 10.1101/gr.6034307
Miller W: Comparison of genomic sequences: solved and unsolved problems. Bioinformatics 2000, 17: 391–397. 10.1093/bioinformatics/17.5.391
Rivas E, Eddy SR: Secondary structure alone is generally not statistically significant for the detection of noncoding RNAs. Bioinformatics 2000, 16: 583–605. 10.1093/bioinformatics/16.7.583
Wang L, Jiang T: On the complexity of multiple sequence alignment. J Comput Biol 1994, 1: 337–348.
Bourque G, Pevzner PA: Genome-scale evolution: reconstructing gene orders in the ancestral species. Genome Res 2002, 12: 26–36.
Pollard DA, Bergman CM, Stoye J, Celniker SE, Eisen MB: Benchmarking tools for the alignment of functional noncoding DNA. BMC Bioinformatics 2004, 5: 6. 10.1186/1471-2105-5-6
Pollard DA, Moses AM, Iyer VN, Eisen MB: Detecting the limits of regulatory element conservation and divergence estimation using pairwise and multiple alignments. BMC Bioinformatics 2006, 7: 376. 10.1186/1471-2105-7-376
Rosenberg MS: Multiple sequence alignment accuracy and evolutionary distance estimation. BMC Bioinformatics 2005, 6: 278. 10.1186/1471-2105-6-278
Thompson JD, Plewniak F, Poch O: A comprehensive comparison of multiple sequence alignment programs. Nucleic Acids Res 1999, 27: 2682–2690. 10.1093/nar/27.13.2682
Blanchette M, Kent WJ, Riemer C, Elnitski L, Smit AF, Roskin KM, Baertsch R, Rosenbloom K, Clawson H, Green ED, Haussler D, Miller W: Aligning multiple genomic sequences with the threaded blockset aligner. Genome Res 2004, 14: 708–715. 10.1101/gr.1933104
Prakash A, Tompa M: Measuring the accuracy of genome-size multiple alignments. Genome Biol 2007, 8: R124. 10.1186/gb-2007-8-6-r124
Brudno M, Do CB, Cooper GM, Kim MF, Davydov E, Green ED, Sidow A, Batzoglou S: LAGAN and Multi-LAGAN: efficient tools for large-scale multiple alignments of genomic DNA. Genome Res 2003, 13(4):721–731. 10.1101/gr.926603
Cline M, Hughey R, Karplus K: Predicting reliable regions in protein sequence alignments. Bioinformatics 2002, 18: 306–314. 10.1093/bioinformatics/18.2.306
Pei J, Grishin NV: AL2CO: calculation of positional conservation in a protein sequence alignment. Bioinformatics 2001, 17: 700–712. 10.1093/bioinformatics/17.8.700
Thompson JD, Plewniak F, Ripp R, Thierry JC, Poch O: Towards a reliable objective function for multiple sequence alignments. J Mol Biol 2001, 314: 937–951. 10.1006/jmbi.2001.5187
Thompson JD, Prigent V, Poch O: LEON: multiple aLignment Evaluation Of Neighbours. Nucleic Acids Res 2004, 32: 1298–1307. 10.1093/nar/gkh294
Eddy SR, Durbin R: RNA Sequence Analysis Using Covariance Models. Nucleic Acids Res 1994, 22: 2079–2088. 10.1093/nar/22.11.2079
Lassmann T, Sonnhammer ELL: Automatic assessment of alignment quality. Nucleic Acids Res 2005, 33: 7120–7128. 10.1093/nar/gki1020
Errami M, Geourjon C, Deléage G: Detection of unrelated proteins in sequences multiple alignments by using predicted secondary structures. Bioinformatics 2003, 19: 506–512. 10.1093/bioinformatics/btg016
Karlin S, Altschul S: Applications and statistics for multiple high-scoring segments in molecular sequences. PNAS 1993, 90: 5873–5877. 10.1073/pnas.90.12.5873
Prakash A, Tompa M: Statistics of local multiple alignments. Bioinformatics 2005, 21: i344-i350. 10.1093/bioinformatics/bti1042
Griffiths-Jones S, Bateman A, Marshall M, Khanna A, Eddy SR: Rfam: an RNA family database. Nucleic Acids Res 2003, 31: 439–441. 10.1093/nar/gkg006
Griffiths-Jones S, Moxon S, Marshall M, Khanna A, Eddy SR, Bateman A: Rfam: annotating non-coding RNAs in complete genomes. Nucleic Acids Res 2005, 33: D121-D124. 10.1093/nar/gki081
Eddy SR: A memory-efficient dynamic programming algorithm for optimal alignment of a sequence to an RNA secondary structure. BMC Bioinformatics 2002, 3: 18. 10.1186/1471-2105-3-18
Kent WJ, Sugnet C, Furey T, Roskin K, Pringle T, Zahler AM, Haussler D: The human genome browser at UCSC. Genome Res 2002, 12: 996–1006. 10.1101/gr.229102. Article published online before print in May 2002
Pedersen JS, Bejerano G, Siepel A, Rosenbloom K, Lindblad-Toh K, Lander ES, Kent J, Miller W, Haussler D: Identification and Classification of Conserved RNA Secondary Structures in the Human Genome. PLoS Comput Biol 2006, 2(4):-e33.
Washietl S, Hofacker IL, Lukasser M, Huttenhofer A, Stadler PF: Mapping of conserved RNA secondary structures predicts thousands of functional noncoding RNAs in the human genome. Nature Biotech 2005, 23: 1383–1390. 10.1038/nbt1144
Siepel A, Bejerano G, Pedersen JS, Hinrichs AS, Hou M, Rosenbloom K, Clawson H, Spieth J, Hillier LW, Richards S, Weinstock GM, Wilson RK, Gibbs RA, Kent WJ, Miller W, Haussler D: Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes. Genome Res 2005, 15: 1034–1050. 10.1101/gr.3715005
Torarinsson E, Sawera M, Havgaard JH, Fredholm M, Gorodkin J: Thousands of corresponding human and mouse genomic regions unalignable in primary sequence contain common RNA structure. Genome Res 2006, 16: 885–889. Erratum: Genome Res. 16:1439 Erratum: Genome Res. 16:1439 10.1101/gr.5226606
Schwartz S, Kent WJ, Smit A, Zhang Z, Baertsch R, Hardison RC, Haussler D, Miller W: Human mouse alignments with BLASTZ. Genome Res 2003, 13: 103–107. 10.1101/gr.809403
Kent WJ, Baertsch R, Hinrichs A, Miller W, Haussler D: Evolution's cauldron: duplication, deletion, and rearrangement in the mouse and human genomes. Proc Natl Acad Sci USA 2003, 100(20):11484–11489. 10.1073/pnas.1932072100
Kent WJ: Blat-the BLAST-like alignment tool. Genome Res 2002, 4: 656–664. 10.1101/gr.229202. Article published online before March 2002
We thank George Asimenos, Michael Brudno, Xu Miao, Amol Prakash, Zasha Weinberg, Zizhen Yao, and the anonymous reviewers for their valuable comments, and Elfar Torarinsson for pointing out the applicability of this approach to annotating aligned genomes. This material is based upon work supported in part by the National Science Foundation under grant DBI-0218798 and by the National Institutes of Health under grants R01 HG02602, T32 HG00035, and P20 GM076222.
AXW wrote all the programs and conducted the experiments. All authors participated in the design of the study, and read and approved the final manuscript.
Authors’ original submitted files for images
Below are the links to the authors’ original submitted files for images.
About this article
Cite this article
Wang, A.X., Ruzzo, W.L. & Tompa, M. How accurately is ncRNA aligned within whole-genome multiple alignments?. BMC Bioinformatics 8, 417 (2007). https://doi.org/10.1186/1471-2105-8-417