The Visitor Facility was first established in 1998, has been regularly updated, and so is extremely well equipped for all molecular population genetic and genomic applications. Visitors are supervised by the NEOF team but also have the opportunity to participate in seminars and to interact with other members of the Evolution, Behaviour and Genomics research cluster. Visits vary in length from days to months.
Access, including consumables, is free to successful applicants (see Eligibility), but we do not support travel and accommodation costs. Users of the Visitor Facility also have free access to the new-generation DNA sequencing that their project requires. While the amount of sequencing is not unlimited, we aim to provide sufficient sequencing to enable users to produce a published output. Potential applicants should initiate a discussion about their proposed project via our enquiry form.
We provide training courses to support a range of capabilities including, for example, genome assembly, metabarcoding, population genomics and RNA sequencing. We aim to support the training that is in most demand from our community. If you wish to request training, register your interest for a course.
These are some of the training courses we are running online in 2021 – registration is now open for Introduction to Sequencing Data & QC, Bacterial 16S metabarcoding & Metabarcoding for diet analysis and environmental DNA.
Introduction to command line bioinformatics - Tue 23 Feb 2021.
Bioinformatics is an increasingly important skill for biological scientists. Many bioinformatic tools can only be run on Unix based operating systems. This course is aimed at beginners and novices to the command line; it will give an overview of fundamental unix commands, directory navigation, and file manipulation. The course will act as a perfect primer for those interested in our other Bioinformatic courses.
Register for this course (deadline 15/02)
Introduction to sequencing data and quality control - Tue 16 & Thu 18 March 2021
There are 3 sequencing technologies that are heavily used for biological research; Illumina, PacBio, and ONT. These three technologies each have their own errors and biases. At the end of this course you will understand these error profiles, and be able to use command line tools to measure sequencing quality and conduct quality control.
Register for this course (deadline 8/03)
Bacterial 16S metabarcoding - Tue 27 & Thu 29 April 2021
Sequencing of the 16S rRNA gene is a well established method of determining the bacterial taxonomic composition of microbiomes. This has been used for human and animal body sites, soil, sewage, clouds, deserts, permafrost and many other environments. This course will give you the ability to describe the advantages and disadvantages of 16S rRNA sequencing, and analyse 16S rRNA datasets with the QIIME2 bioinformatics platform.
Register for this course (deadline 19/04)
Metabarcoding for diet analysis and environmental DNA - Tue 18 & Thu 20 May 2021
Sequencing DNA barcodes from mixed sources of DNA is an increasingly used way to survey biodiversity, whether analysing dietary content from faecal-derived DNA or monitoring aquatic species from water-derived DNA. This course will give an overview of metabarcoding with different barcoding genes to target particular taxa. Using an example data set we will go from raw sequence data through to assigning taxonomy to the sequence variants.
Register for this course (deadline 10/05)
Microbial shotgun metagenomics - Tue 1 & Thu 3 June 2021
There are many unknown and unculturable microbes found in a vast array of different environments. Shotgun metagenomics is an approach to capture all the genetic information in a sample, providing the taxonomic and metabolic information of all present organisms. In this course we will analyse shotgun metagenomic sequencing data from stool samples to compare western and Korean diets. At the end of the course you will be able to quantify the taxonomic composition with Kraken2 & Bracken, and determine the metabolic profile with the bioBakery suite of tools.
Population genomics - Tue 13 & Thu 15 July 2021
This course will introduce participants to a variety of population genomics analyses for large next generation sequencing (NGS) datasets. It will include discussion on single nucleotide polymorphism (SNP) calling and filtering options, an introduction to population genomics statistics, examining genetic structure, and Fst-based analyses such as outlier detection/genomic islands of divergence.
Bacterial genome assembly and annotation - Tue 3 & Thu 5 Aug 2021
With the advent and improvement of long read sequencing technologies, bacterial genome assembly and annotation is easier and more effective than ever. At the end of this course you will be able to perform genome assembly and polishing of PacBio sequencing followed by annotation with prokka. Additionally you will be able to assess the quality of the genome with contiguity measures from QUAST and genome completeness estimation with BUSCO.
Eukaryote and large genome assembly and annotation
Many eukaryotic genomes are larger and more complex than bacterial genomes, requiring different tools for optimal genome assembly and annotation. This course will give an overview of long read genome assembly and polishing followed by scaffolding and gap filling. We will then assess the contiguity and completeness of the assembly with QUAST and BUSCO. Finally we will annotate the genome assembly with the annotation pipeline MAKER.
RNA-seq gene expression and pathway analysis
RNA-Seq (AKA whole transcriptomic shotgun sequencing) aims to determine the presence and quantity of RNA in a biological sample at a given moment in time. This allows you to determine the level of expression of these genes and therefore compare these expressions across different sample groups, i.e. Differential Gene Expression (DGE). At the end of this course you will be able to align the transcriptomes of samples to a reference genome to determine gene expression levels. Following this you will be able to carry out Differential Gene Expression analysis to determine which genes are up and down regulated between sample groups.
Empowering the next generation of environmental researchers.
If you would like more information about NEOF and the services we offer, or make any other enquiry, please complete our form.