scholarly journals Interactive Tree Of Life (iTOL) v5: an online tool for phylogenetic tree display and annotation

2021 ◽  
Author(s):  
Ivica Letunic ◽  
Peer Bork

Abstract The Interactive Tree Of Life (https://itol.embl.de) is an online tool for the display, manipulation and annotation of phylogenetic and other trees. It is freely available and open to everyone. iTOL version 5 introduces a completely new tree display engine, together with numerous new features. For example, a new dataset type has been added (MEME motifs), while annotation options have been expanded for several existing ones. Node metadata display options have been extended and now also support non-numerical categorical values, as well as multiple values per node. Direct manual annotation is now available, providing a set of basic drawing and labeling tools, allowing users to draw shapes, labels and other features by hand directly onto the trees. Support for tree and dataset scales has been extended, providing fine control over line and label styles. Unrooted tree displays can now use the equal-daylight algorithm, proving a much greater display clarity. The user account system has been streamlined and expanded with new navigation options and currently handles >1 million trees from >70 000 individual users.

2019 ◽  
Vol 47 (W1) ◽  
pp. W256-W259 ◽  
Author(s):  
Ivica Letunic ◽  
Peer Bork

Abstract The Interactive Tree Of Life (https://itol.embl.de) is an online tool for the display, manipulation and annotation of phylogenetic and other trees. It is freely available and open to everyone. The current version introduces four new dataset types, together with numerous new features. Annotation options have been expanded and new control options added for many display elements. An interactive spreadsheet-like editor has been implemented, providing dataset creation and editing directly in the web interface. Font support has been rewritten with full support for UTF-8 character encoding throughout the user interface. Google Web Fonts are now fully supported in the tree text labels. iTOL v4 is the first tool which supports direct visualization of Qiime 2 trees and associated annotations. The user account system has been streamlined and expanded with new navigation options, and currently handles >700 000 trees from more than 40 000 individual users. Full batch access has been implemented allowing programmatic upload and export of trees and annotations.


2021 ◽  
Vol 4 ◽  
Author(s):  
Haris Zafeiropoulos ◽  
Laura Gargan ◽  
Christina Pavloudi ◽  
Evangelos Pafilis ◽  
Jens Carlsson

Environmental DNA (eDNA) metabarcoding has been commonly used in recent years (Jeunen et al. 2019) for the identification of the species composition of environmental samples. By making use of genetic markers anchored in conserved gene regions, universally present acrooss the species of large taxonomy groups, eDNA metabarcoding exploits both extra- and intra-cellular DNA fragments for biodiversity assessment. However, there is not a truly “universal” marker gene that is capable of amplifying all species across different taxa (Kress et al. 2015). The mitochondrial cytochrome C oxidase subunit I gene (COI) has many of the desirable properties of a “universal" marker and has been widely used for assessing species identity in Eukaryotes, especially metazoans (Andjar et al. 2018). However, a great number of COI Operational Taxonomic Units (OTUs) or/and Amplicon Sequence Variants (ASVs) retrieved from such studies do not match reference sequences and are often referred to as “dark matter” (Deagle et al. 2014). The aim of this study was to discover the origins and identities of these COI dark matter sequences. We built a reference phylogenetic tree that included as many COI-sequence-related information across the tree of life as possible. An overview of the steps followed is presented in Fig. 1a. Briefly, the Midori reference 2 database was used to retrieve eukaryotes sequences (183,330 species). In addition, the API of the BOLD database was used as source for the corresponding Bacteria (559 genera) and Archaea (41 genera) sequences. Consensus sequences at the family level were constructed from each of these three initial COI datasets. The COI-oriented reference phylogenetic tree of life was then built by using 1,240 consensus sequences with more than 80% of those coming from eukaryotic taxa. Phylogeny-based taxonomic assignment was then used to place query sequences. The a) total number of sequences, b) sequences assigned to Eukaryotes and c) unassigned subsets of OTUs, from marine and freshwater samples, retrieved during in-house metabarcoding experiments, were placed in the reference tree (Fig. 1b). It is clear that a large proportion of sequences targeting the COI region of Eukaryotes actually represents bacterial branches in the phylogenetic tree (Fig. 1b). We conclude that COI metabarcoding studies targeting Eukaryotes may come with a great bias derived from amplification and sequencing of bacterial taxa, depending on the primer pair used. However, for the time being, publicly available bacterial COI sequences are far too few to represent the bacterial variability; thus, a reliable taxonomic identification of them is not possible. We suggest that bacterial COI sequences should be included in the reference databases used for the taxonomy assignment of OTUs/ASVs in COI-based eukaryote metabarcoding studies to allow for bacterial sequences that were amplified to be excluded enabling researchers to exclude non-target sequences. Further, the approach presented here allows researchers to better understand the unknown unknowns and shed light on the dark matter of their metabarcoding sequence data.


2009 ◽  
Vol 7 (8) ◽  
pp. 615-615 ◽  
Author(s):  
Ethan B. Ludmir ◽  
Lynn W. Enquist

2015 ◽  
Vol 370 (1678) ◽  
pp. 20140336 ◽  
Author(s):  
Tom A. Williams ◽  
Sarah E. Heaps ◽  
Svetlana Cherlin ◽  
Tom M. W. Nye ◽  
Richard J. Boys ◽  
...  

The root of a phylogenetic tree is fundamental to its biological interpretation, but standard substitution models do not provide any information on its position. Here, we describe two recently developed models that relax the usual assumptions of stationarity and reversibility, thereby facilitating root inference without the need for an outgroup. We compare the performance of these models on a classic test case for phylogenetic methods, before considering two highly topical questions in evolutionary biology: the deep structure of the tree of life and the root of the archaeal radiation. We show that all three alignments contain meaningful rooting information that can be harnessed by these new models, thus complementing and extending previous work based on outgroup rooting. In particular, our analyses exclude the root of the tree of life from the eukaryotes or Archaea, placing it on the bacterial stem or within the Bacteria. They also exclude the root of the archaeal radiation from several major clades, consistent with analyses using other rooting methods. Overall, our results demonstrate the utility of non-reversible and non-stationary models for rooting phylogenetic trees, and identify areas where further progress can be made.


mSystems ◽  
2021 ◽  
Vol 6 (1) ◽  
Author(s):  
Victor Gambarini ◽  
Olga Pantos ◽  
Joanne M. Kingsbury ◽  
Louise Weaver ◽  
Kim M. Handley ◽  
...  

ABSTRACT The number of plastic-degrading microorganisms reported is rapidly increasing, making it possible to explore the conservation and distribution of presumed plastic-degrading traits across the diverse microbial tree of life. Putative degraders of conventional high-molecular-weight polymers, including polyamide, polystyrene, polyvinylchloride, and polypropylene, are spread widely across bacterial and fungal branches of the tree of life, although evidence for plastic degradation by a majority of these taxa appears limited. In contrast, we found strong degradation evidence for the synthetic polymer polylactic acid (PLA), and the microbial species related to its degradation are phylogenetically conserved among the bacterial family Pseudonocardiaceae. We collated data on genes and enzymes related to the degradation of all types of plastic to identify 16,170 putative plastic degradation orthologs by mining publicly available microbial genomes. The plastic with the largest number of putative orthologs, 10,969, was the natural polymer polyhydroxybutyrate (PHB), followed by the synthetic polymers polyethylene terephthalate (PET) and polycaprolactone (PCL), with 8,233 and 6,809 orthologs, respectively. These orthologous genes were discovered in the genomes of 6,000 microbial species, and most of them are as yet not identified as plastic degraders. Furthermore, all these species belong to 12 different microbial phyla, of which just 7 phyla have reported degraders to date. We have centralized information on reported plastic-degrading microorganisms within an interactive and updatable phylogenetic tree and database to confirm the global and phylogenetic diversity of putative plastic-degrading taxa and provide new insights into the evolution of microbial plastic-degrading capabilities and avenues for future discovery. IMPORTANCE We have collated the most complete database of microorganisms identified as being capable of degrading plastics to date. These data allow us to explore the phylogenetic distribution of these organisms and their enzymes, showing that traits for plastic degradation are predominantly not phylogenetically conserved. We found 16,170 putative plastic degradation orthologs in the genomes of 12 different phyla, which suggests a vast potential for the exploration of these traits in other taxa. Besides making the database available to the scientific community, we also created an interactive phylogenetic tree that can display all of the collated information, facilitating visualization and exploration of the data. Both the database and the tree are regularly updated to keep up with new scientific reports. We expect that our work will contribute to the field by increasing the understanding of the genetic diversity and evolution of microbial plastic-degrading traits.


Astrobiology ◽  
2000 ◽  
pp. 195-211 ◽  
Author(s):  
Raimundo Villegas ◽  
Cecilia Castillo ◽  
Gloria M. Villegas

2013 ◽  
Vol 5 (1) ◽  
pp. 10-16
Author(s):  
M. N. Shiva Kameshwari ◽  
H. L. Geetha ◽  
K. J. Tharasaraswathi

In the present study on Urginea indica, twelve different populations from southern part of India is considered. Fifteen parameters have been scored for each population to understand the relationship between different races. The main objective is to trace phylogeny in populations of U. indica to construct phylogenetic tree. The phylogenetic tree obtained is an unrooted tree. The parsimony tree describes that Shimoga and Chamundi hill populations have parallely evolved and forms the out group. Dopaegowdanapura population has given rise to Gopalaswamy betta, Gopalaswamy betta has given rise to Banganavadi and Banganavadi has given rise to one population which is missing in the tree and the missing population has given rise to Gorur on one hand and to Krishna Raja Sagar island and Gandhi Krishi Vighnayana Kendra on the other hand. Krishna Raja Sagar island and Gandhi Krishi Vighnayana Kendra shares a common clade. Gorur has given rise to Papanasini and Papanasini has given rise to Channamallipura, from Channamallipura another population has been evolved which is missing and the missing population has given rise to Basavanahalli and Ranganthittu which shares a Common clade. The Parsimony tree shows that these populations have evolved parallel. Dopaegowdanapura is the oldest from which all others are evolved. Ranganathittu and Basavanahalli form the youngest and latest. Therefore it is an unrooted tree with distance. Each population varied in their morphology and chromosome number and called as cytotypes. Difference in morphological character is mainly because of genetic characters. Habitat does not seem to play major role to mould morphological features.


Sign in / Sign up

Export Citation Format

Share Document