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Mark Blaxter

Publications and source records attributed to Mark Blaxter.

5 recordsLinked to original sources

Lepbase: the Lepidopteran genome database

As the generation and use of genomic datasets is becoming increasingly common in all areas of biology, the need for resources to collate, analyse and present data from independent (Tier 1) species-level genome projects into well supported clade-oriented (Tier 2) databases and provide a mechanism for these data to be propagated to pan-taxonomic (Tier 3) databases is becoming more pressing. Lepbase is a Tier 2 genomic resource for the Lepidoptera, supporting a research community using genomic approaches to understand evolution, speciation, olfaction, behaviour and pesticide resistance in a wide range of target species. Lepbase offers a core set of tools to make genomic data widely accessible including an Ensembl genome browser, text and sequence homology searches and bulk downloads of consistently presented and formatted datasets. As a part of the taxonomic community that we serve, we are working directly with Lepidoptera researchers to prioritise analyses and add tools that will be of most value to current research questions.

Bioinformatics

Purifying selection and drift, not life history or RNAi, determine transposable element evolution

Transposable elements (TEs) are a major source of genome variation across the branches of life. Although TEs may occasionally play an adaptive role in their hosts genome, they are much more often deleterious, and purifying selection is thus an important factor controlling genomic TE loads. In contrast, life history and genomic characteristics such as mating system, parasitism, GC content, and RNAi pathways, have been suggested to account for the startling disparity of TE loads in different species. Previous studies of fungal, plant, and animal genomes have reported conflicting results regarding the direction in which these genomic features drive TE evolution. Many of these studies have had limited power because they studied taxonomically narrow systems, comparing only a limited number of phylogenetically independent contrasts, and did not address long term effects on TE evolution. Here we explicitly test the long term determinants of TE evolution by comparing 42 nematode genomes that span over 500 million years of diversification, and include numerous transitions between life history states and RNAi pathways. We have analysed the reconstructed TE loads of ancestors through the Nematoda phylogeny to account for correlation with GC content and transitions in TE evolutionary models. We also analysed the effect of transitions in life history characteristics and RNAi using ANOVA of phylogenetically independent contrasts. We show that purifying selection against TEs is the dominant force throughout the evolutionary history of Nematoda, as indicated by reconstructed ancestral TE loads, and that strong stochastic Ornstein-Uhlenbeck processes are the underlying models which best explain TE diversification among extant species. In contrast we found no evidence that life history or RNAi variations have a significant influence upon genomic TE load across extended periods of evolutionary history. We suggest that these are largely inconsequential to the large differences in TE content observed between genomes and only by these large-scale comparisons can we distinguish long term and persistent effects from transient effects or misleading random changes.

Evolutionary Biology

No evidence for extensive horizontal gene transfer in the genome of the tardigrade Hypsibius dujardini

Tardigrades are meiofaunal ecdysozoans that are key to understanding the origins of Arthropoda. Many species of Tardigrada can survive extreme conditions through cryptobiosis. In a recent paper (Boothby TC et al (2015) Evidence for extensive horizontal gene transfer from the draft genome of a tardigrade. Proc Natl Acad Sci USA 112:15976-15981) the authors concluded that the tardigrade Hypsibius dujardini had an unprecedented proportion (17%) of genes originating through functional horizontal gene transfer (fHGT), and speculated that fHGT was likely formative in the evolution of cryptobiosis. We independently sequenced the genome of H. dujardini. As expected from whole-organism DNA sampling, our raw data contained reads from non-target genomes. Filtering using metagenomics approaches generated a draft H. dujardini genome assembly of 135 Mb with superior assembly metrics to the previously published assembly. Additional microbial contamination likely remains. We found no support for extensive fHGT. Among 23,021 gene predictions we identified 0.2% strong candidates for fHGT from bacteria, and 0.2% strong candidates for fHGT from non-metazoan eukaryotes. Cross-comparison of assemblies showed that the overwhelming majority of HGT candidates in the Boothby et al. genome derived from contaminants. We conclude that fHGT into H. dujardini accounts for at most 1-2% of genes and that the proposal that one sixth of tardigrade genes originate from functional HGT events is an artefact of undetected contamination.

Genomics

A single chromosome assembly of Bacteroides fragilis strain BE1 from Illumina and MinION nanopore sequencing data

BackgroundSecond and third generation sequencing technologies have revolutionised bacterial genomics. Short-read Illumina reads result in cheap but fragmented assemblies, whereas longer reads are more expensive but result in more complete genomes. The Oxford Nanopore MinION device is a revolutionary mobile sequencer that can produce thousands of long, single molecule reads.\n\nResultsWe sequenced Bacteroides fragilis strain BE1 using both the Illumina MiSeq and Oxford Nanopore MinION platforms. We were able to assemble a single chromosome of 5.18 Mb, with no gaps, using publicly available software and commodity computing hardware. We identified gene rearrangements and the state of invertible promoters in the strain.\n\nConclusionsThe single chromosome assembly of Bacteroides fragilis strain BE1 was achieved using only modest amounts of data, publicly available software and commodity computing hardware. This combination of technologies offers the possibility of ultra-cheap, high quality, finished bacterial genomes.

Genomics

poRe: an R package for the visualization and analysis of nanopore sequencing data

MotivationThe Oxford Nanopore MinION device represents a unique sequencing technology. As a mobile sequencing device powered by the USB port of a laptop, the MinION has huge potential applications. To enable these applications, the bioinformatics community will need to design and build a suite of tools specifically for MinION data.\n\nResultsHere we present poRe, a package for the statistical software R that enables users to manipulate, organize, summarise and visualize MinION nanopore sequencing data. As a packge for R, poRe has been tested on both Windows and Linux. Crucially, the Windows version allows users to analyse MinION data on the Windows laptop attached to the device\n\nAvailabilityPre-built R packages for Windows and Linux are available under a BSD license at http://sourceforge.net/projects/rpore/\n\nContactmick.watson@roslin.ed.ac.uk

Bioinformatics