Ultra-large alignments using Phylogeny-aware Profiles

Many biological questions, including the estimation of deep evolutionary histories and the detection of remote homology between protein sequences, rely upon multiple sequence alignments (MSAs) and phylogenetic trees of large datasets. However, accurate large-scale multiple sequence alignment is very difficult, especially when the dataset contains fragmentary sequences. We present UPP, an MSA method that uses a new machine learning technique - the Ensemble of Hidden Markov Models - that we propose here. UPP produces highly accurate alignments for both nucleotide and amino acid sequences, even on ultra-large datasets or datasets containing fragmentary sequences. UPP is available at https://github.com/smirarab/sepp.Comment: Online supplemental materials and data are available at http://www.cs.utexas.edu/users/phylo/software/upp

Evolutionary and molecular foundations of multiple contemporary functions of the nitroreductase superfamily.

Insight regarding how diverse enzymatic functions and reactions have evolved from ancestral scaffolds is fundamental to understanding chemical and evolutionary biology, and for the exploitation of enzymes for biotechnology. We undertook an extensive computational analysis using a unique and comprehensive combination of tools that include large-scale phylogenetic reconstruction to determine the sequence, structural, and functional relationships of the functionally diverse flavin mononucleotide-dependent nitroreductase (NTR) superfamily (>24,000 sequences from all domains of life, 54 structures, and >10 enzymatic functions). Our results suggest an evolutionary model in which contemporary subgroups of the superfamily have diverged in a radial manner from a minimal flavin-binding scaffold. We identified the structural design principle for this divergence: Insertions at key positions in the minimal scaffold that, combined with the fixation of key residues, have led to functional specialization. These results will aid future efforts to delineate the emergence of functional diversity in enzyme superfamilies, provide clues for functional inference for superfamily members of unknown function, and facilitate rational redesign of the NTR scaffold

Characterization of the definitive classical calpain family of vertebrates using phylogenetic, evolutionary and expression analyses

Peer reviewedPublisher PD

Alignment uncertainty, regressive alignment and large scale deployment

A multiple sequence alignment (MSA) provides a description of the relationship between biological sequences where columns represent a shared ancestry through an implied set of evolutionary events. The majority of research in the field has focused on improving the accuracy of alignments within the progressive alignment framework and has allowed for powerful inferences including phylogenetic reconstruction, homology modelling and disease prediction. Notwithstanding this, when applied to modern genomics datasets - often comprising tens of thousands of sequences - new challenges arise in the construction of accurate MSA. These issues can be generalised to form three basic problems. Foremost, as the number of sequences increases, progressive alignment methodologies exhibit a dramatic decrease in alignment accuracy. Additionally, for any given dataset many possible MSA solutions exist, a problem which is exacerbated with an increasing number of sequences due to alignment uncertainty. Finally, technical difficulties hamper the deployment of such genomic analysis workflows - especially in a reproducible manner - often presenting a high barrier for even skilled practitioners. This work aims to address this trifecta of problems through a web server for fast homology extension based MSA, two new methods for improved phylogenetic bootstrap supports incorporating alignment uncertainty, a novel alignment procedure that improves large scale alignments termed regressive MSA and finally a workflow framework that enables the deployment of large scale reproducible analyses across clusters and clouds titled Nextflow. Together, this work can be seen to provide both conceptual and technical advances which deliver substantial improvements to existing MSA methods and the resulting inferences.Un alineament de seqüència múltiple (MSA) proporciona una descripció de la relació entre seqüències biològiques on les columnes representen una ascendència compartida a través d'un conjunt implicat d'esdeveniments evolutius. La majoria de la investigació en el camp s'ha centrat a millorar la precisió dels alineaments dins del marc d'alineació progressiva i ha permès inferències poderoses, incloent-hi la reconstrucció filogenètica, el modelatge d'homologia i la predicció de malalties. Malgrat això, quan s'aplica als conjunts de dades de genòmica moderns, que sovint comprenen desenes de milers de seqüències, sorgeixen nous reptes en la construcció d'un MSA precís. Aquests problemes es poden generalitzar per formar tres problemes bàsics. En primer lloc, a mesura que augmenta el nombre de seqüències, les metodologies d'alineació progressiva presenten una disminució espectacular de la precisió de l'alineació. A més, per a un conjunt de dades, existeixen molts MSA com a possibles solucions un problema que s'agreuja amb un nombre creixent de seqüències a causa de la incertesa d'alineació. Finalment, les dificultats tècniques obstaculitzen el desplegament d'aquests fluxos de treball d'anàlisi genòmica, especialment de manera reproduïble, sovint presenten una gran barrera per als professionals fins i tot qualificats. Aquest treball té com a objectiu abordar aquesta trifecta de problemes a través d'un servidor web per a l'extensió ràpida d'homologia basada en MSA, dos nous mètodes per a la millora de l'arrencada filogenètica permeten incorporar incertesa d'alineació, un nou procediment d'alineació que millora els alineaments a gran escala anomenat MSA regressivu i, finalment, un marc de flux de treball permet el desplegament d'anàlisis reproduïbles a gran escala a través de clústers i computació al núvol anomenat Nextflow. En conjunt, es pot veure que aquest treball proporciona tant avanços conceptuals com tècniques que proporcionen millores substancials als mètodes MSA existents i les conseqüències resultants