Micro binfie podcast

Micro binfie podcast

By Microbial BioinformaticsScience
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Micro binfie podcast episodes

  • 48 SARS-CoV-2 More Variants of Concern and updates from Africa
    We discuss the latest developments in SARS-CoV-2 genomics over the last 2 weeks with Peter van Heusden, covering the growing list of Variants of Concern and the latest developments in Africa.
    Papers & resources mentioned:
    American birds (677) - https://www.medrxiv.org/content/10.1101/2021.02.12.21251658v2
    https://github.com/cov-lineages/pango-designation
    PHE thresholds for different variants:
    https://www.gov.uk/government/publications/covid-19-variants-genomically-confirmed-case-numbers/variants-distribution-of-cases-data
    A.23.1 in Uganda - https://www.medrxiv.org/content/10.1101/2021.02.08.21251393v1
    B.1.525 - https://github.com/cov-lineages/pango-designation/issues/4
    Zambia sequences -
    https://www.cdc.gov/mmwr/volumes/70/wr/mm7008e2.htm?s_cid=mm7008e2_w
    29 min
  • 47 SARS-CoV-2 Rapid roundup and questions answered
    We present a rapid round up of SARS-CoV-2 questions and issues, hopefully with some answers, so that you can stay on top of the latest in SARS-CoV-2 genomics. Recorded 5 February 2021.
    Topics covered:
    Why missing 1 SNP can cause lineage assignment to break and how it works?
    How do we describe lineages with a chain of mutation events?
    Are we seeing convergent evolution?
    Co-infections of different lineages discovered?
    For nanopore basecalling do use HAC & should you get a GPU?
    Basic logistics difficult for sequencing in many parts of world.
    Can I look at recombination with ARTIC on Illumina?
    How do you annotate a SARS-CoV-2 sequence?
    http://cov-glue.cvr.gla.ac.uk/#/home
    FASTA > nextclade
    VCF > snpeff
    https://github.com/cov-ert/type_variants
    Spotting community spread from NextStrain?
    Scientists call for fully open sharing of coronavirus genome data: https://www.nature.com/articles/d41586-021-00305-7
    33 min
  • 46 SARS-CoV-2 genomics resources
    We discuss recent updates to the best SARS-CoV-2 resources, so that you can stay on top of the latest bioinformatics and genomics tools. Recorded 5 February 2021.
    CoVariants website: http://covariants.org/
    Microreact: https://microreact.org/project/cogconsortium/
    Lineage reports: https://cov-lineages.org/
    CLIMB ARTIC workshop online resources: https://www.climb.ac.uk/artic-and-climb-big-data-joint-workshop/
    Multiplex PCR for B.1.1.7, B.1.351 and P.1: https://www.protocols.io/view/multiplexed-rt-qpcr-to-screen-for-sars-cov-2-b-1-1-brrhm536
    CDC videos: https://www.cdc.gov/amd/training/covid-19-gen-epi-toolkit.html
    24 min
  • 45 Software deep dive: Enterobase
    We chat with Nabil about EnteroBase, and learn about the background to the project, the general benefits of the platforms and some of the strange quirks users might encounter. EnteroBase is an integrated software environment that supports the identification of global population structures within several bacterial genera that include pathogens.
    Papers:
    Mentioned PLOS genetics paper:
    Alikhan et al. (2018) A genomic overview of the population structure of Salmonella. PLoS Genet 14 (4): e1007261 https://doi.org/10.1371/journal.pgen.1007261
    Paper describing Enterobase and the genome fishing expeditions:
    Zhou et al. (2020) The EnteroBase user's guide, with case studies on Salmonella transmissions, Yersinia pestis phylogeny and Escherichia core genomic diversity. Genome Res. 30:138-152. https://doi.org/10.1101/gr.251678.119
    rMLST is described in: Jolley et al. 2012 Microbiology 158:1005-15. https://doi.org/10.1099/mic.0.055459-0
    Resources
    Enterobase: http://enterobase.warwick.ac.uk/
    PubMLST https://pubmlst.org/
    About EnteroBase schemes: https://enterobase.readthedocs.io/en/latest/enterobase-tutorials/deeper-lineages.html
    Software:
    Enterobase toolkit and background software: https://github.com/zheminzhou/EToKi
    Errata.
    Jay Hinton’s Salmonella is a ST313 (D23580), not ST131 (I always mix the numbers up -- Nabil)
    21 min
  • 44 How to sequence SARS-CoV-2 using the ARTIC protocol with Joshua Quick
    Joshua Quick from the University of Birmingham talks about "How to sequence SARS-CoV-2 using the ARTIC protocol".
    This was part of a joint ARTICnetwork & CLIMB-BIG-DATA workshop on COVID-19 data analysis and chaired by Nick Loman.
    Links:
    https://twitter.com/Scalene/status/1349402397249056779
    https://primalscheme.com/
    https://www.protocols.io/view/ncov-2019-sequencing-protocol-v3-locost-bh42j8ye
    https://github.com/artic-network/rampart
    23 min
  • 43 Why use genomics in an epidemic? with Sam Sheppard
    Sam Sheppard from the University of Bath presents at the ARTICnetwork & CLIMB-BIG-DATA workshop on COVID-19 data analysis, motivating why we should use genomics in an epidemic.
    He gives background on typing schemes, different ways of sequencing and challenges such as how you can analyse large mounts of genomic data.
    Resources:
    https://sheppardlab.com/
    https://www.climb.ac.uk/artic-and-climb-big-data-joint-workshop/
    19 min
  • 42 Overcoming barriers to SARS-CoV-2 data analysis
    ARTICnetwork & CLIMB-BIG-DATA present a panel discussion on overcoming barriers to SARS-CoV-2 data analysis with Nick Loman and Will Rowe from the University of Birmingham, Áine O'Toole from the University of Edinburgh, Andrew Page from the Quadram Institute and Anna Price from MRC CLIMB and Cardiff University. This was part of a workshop on COVID-19 data analysis.
    Topics covered:
    Collecting sample metadata
    intrapatient variability
    Building bridges with policy makers to start sequencing
    Data sharing
    Improving bioinformatics skills
    Pipeline and software validation
    Bioinformatics reproducibility and quality
    Papers:
    The PHA4GE SARS-CoV-2 Contextual Data Specification for Open Genomic Epidemiology https://www.preprints.org/manuscript/202008.0220/v1
    MAJORA: Continuous integration supporting decentralised sequencing for SARS-CoV-2 genomic surveillance https://www.biorxiv.org/content/10.1101/2020.10.06.328328v1
    Genomic sequencing of SARS-CoV-2: a guide to implementation for maximum impact on public health https://www.who.int/publications/i/item/9789240018440
    Resources:
    https://www.climb.ac.uk/artic-and-climb-big-data-joint-workshop/
    https://github.com/SamStudio8/majora
    https://soundcloud.com/microbinfie/majora
    https://github.com/pha4ge/SARS-CoV-2-Contextual-Data-Specification
    https://pha4ge.org/
    Software:
    https://github.com/cov-lineages/pangolin
    https://github.com/artic-network/civet
    https://github.com/COG-UK/grapevine
    https://github.com/cov-lineages/pangoLEARN
    47 min
  • 41 SARS-CoV-2 Phylogenomics questions answered
    ARTICnetwork & CLIMB-BIG-DATA present a panel discussion on SARS-CoV-2 phylogenomics with Nick Loman from the University of Birmingham, Verity Hill from the University of Edinburgh, Andrew Page from the Quadram Institute and Anna Price from MRC CLIMB and Cardiff University. This was part of a workshop on COVID-19 data analysis.
    The topics covered are:
    More about Polecat
    Whats the difference between COG-UK Phylotypes and Pangolin lineages?
    What is the difference between Civet and Llama
    Can you use BLAST to find similar SARS-CoV-2 genomes?
    How do you find similar sequences in the public repositories to give your samples context?
    How do you manually curate the dataset for PangoLEARN?
    How does Civet choose what constitutes a subtree?
    Can Civet be adapted to other viruses?
    Are the vaccine sequences available?
    Databases that report variation
    Quality of variant calls?
    Groups:
    https://www.climb.ac.uk/artic-and-climb-big-data-joint-workshop/
    https://www.climb.ac.uk/
    https://artic.network/
    https://cogconsortium.uk/
    Software:
    https://github.com/COG-UK/polecat
    https://github.com/cov-lineages/pangolin
    https://github.com/cov-lineages/llama
    https://github.com/artic-network/civet
    https://github.com/cov-lineages/pangoLEARN
    http://tree.bio.ed.ac.uk/software/figtree/
    Analysis websites:
    https://cov-lineages.org/
    https://clades.nextstrain.org/
    https://pangolin.cog-uk.io/
    http://cov-glue.cvr.gla.ac.uk/
    26 min
  • 40 A crash course in SARS-CoV-2 bioinformatics
    Over the last year we've learnt a lot about SARS-CoV-2 genomics. Lee extracts all the insider knowledge from our brains and we give him the honest truth to his probing questions.
    We cover:
    Pipelines for SARS-CoV-2
    Archives & metadata
    Read filtering
    Assembly vs consensus
    Amplicon data analysis
    Controls
    If things look too good
    Coverage
    ....
    Some URLs:
    https://github.com/connor-lab/ncov2019-artic-nf
    https://github.com/jts/ncov-tools
    https://github.com/lskatz/SARS-CoV-2-trueTree
    58 min
  • 39 Explaining the naming of SARS-CoV-2 new variants
    Andrew talks to Niamh Tumelty from the University of Cambridge about SARS-CoV-2 'new variants' and tries to clear up some of the confusion around all the names flying around. Hopefully this helps to give some insights into the various names you hear, but probably by the time you listen the whole thing will have changed again since this field moves so rapidly. Andrew apologises in advance for all the errors that will be found in this podcast!
    If you want to read a bit more theres an interesting news item on Nature: https://www.nature.com/articles/d41586-021-00097-w
    21 min

About Micro binfie podcast

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Microbial Bioinformatics is a rapidly changing field marrying computer science and microbiology. Join us as we share some tips and tricks we’ve learnt over the years. If you’re student just getting to grips to the field, or someone who just wants to keep tabs on the latest and greatest - this podcast is for you.

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