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102 Early days of MLST

40:15
 
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Manage episode 357586619 series 3381906
Micro Binfie Podcast and Microbial Bioinformatics에서 제공하는 콘텐츠입니다. 에피소드, 그래픽, 팟캐스트 설명을 포함한 모든 팟캐스트 콘텐츠는 Micro Binfie Podcast and Microbial Bioinformatics 또는 해당 팟캐스트 플랫폼 파트너가 직접 업로드하고 제공합니다. 누군가가 귀하의 허락 없이 귀하의 저작물을 사용하고 있다고 생각되는 경우 여기에 설명된 절차를 따르실 수 있습니다 https://ko.player.fm/legal.
Ed Feil is a professor of bacterial evolution at the University of Bath, and Natacha Couto, a data scientist at the Center of Genomic Pathogen Surveillance at the University of Oxford. We delve into the concept of multi-locus sequence typing (MLST) in bacterial population genetics. They highlight how the MLST method allows for defining strains based on partial sequences that range up to 500 base pairs. The method measures differences between loci for each strain, offering an allele number while assigning similar numbers to identical sequences. The cumulative sequence number represents the unique identification, which is subsequently referred to as the sequence type (SST). MLST has revolutionized the field by facilitating digital storage and comparison of epidemiological databases, proving particularly useful in investigating transmission events and dissemination of certain strains. Although there are other methods such as Pulse Field Gen Electrophoresis (PFGE) that offer higher resolution when looking for similarities between different strains, MLST remains a versatile and widely used method. They also talk about the shortcomings of MLST and the need for continued improvements in population genetics research. They mention the development of the Eburst program, which uses a circular model, rather than the traditional dendrogram tree structure, to better visualize MLST data and understand the clonal expansion of populations. They also discuss how the original MLST schemes may not have included the best genes for all bacterial species as the genes were chosen before genome sequencing became widely available. Ed and Natacha further elaborate on the concept of clonality among bacterial species. Ed suggests that bacterial population structures have no consistent pattern, with some organisms being well-behaved, while others have a lot of allele shuffling. However, clones have existed since day one, and their presence is still seen today. Natacha adds that although MLST has flaws, it leaves behind the nomenclature for the lineages or clones, which is a lasting legacy. Nabil-Fareed notes that while most reference labs have moved on to genomics, some people still use MLST. He adds that the pipeline is the same for any organism, and the process is efficient in the end. The discussion concludes with the hosts thanking the guests and promising more exciting topics in their next episode. Overall, the hosts highlight the significance of understanding the limitations of MLST and the scope for further research in bacterial population genetics.
  continue reading

139 에피소드

Artwork
icon공유
 
Manage episode 357586619 series 3381906
Micro Binfie Podcast and Microbial Bioinformatics에서 제공하는 콘텐츠입니다. 에피소드, 그래픽, 팟캐스트 설명을 포함한 모든 팟캐스트 콘텐츠는 Micro Binfie Podcast and Microbial Bioinformatics 또는 해당 팟캐스트 플랫폼 파트너가 직접 업로드하고 제공합니다. 누군가가 귀하의 허락 없이 귀하의 저작물을 사용하고 있다고 생각되는 경우 여기에 설명된 절차를 따르실 수 있습니다 https://ko.player.fm/legal.
Ed Feil is a professor of bacterial evolution at the University of Bath, and Natacha Couto, a data scientist at the Center of Genomic Pathogen Surveillance at the University of Oxford. We delve into the concept of multi-locus sequence typing (MLST) in bacterial population genetics. They highlight how the MLST method allows for defining strains based on partial sequences that range up to 500 base pairs. The method measures differences between loci for each strain, offering an allele number while assigning similar numbers to identical sequences. The cumulative sequence number represents the unique identification, which is subsequently referred to as the sequence type (SST). MLST has revolutionized the field by facilitating digital storage and comparison of epidemiological databases, proving particularly useful in investigating transmission events and dissemination of certain strains. Although there are other methods such as Pulse Field Gen Electrophoresis (PFGE) that offer higher resolution when looking for similarities between different strains, MLST remains a versatile and widely used method. They also talk about the shortcomings of MLST and the need for continued improvements in population genetics research. They mention the development of the Eburst program, which uses a circular model, rather than the traditional dendrogram tree structure, to better visualize MLST data and understand the clonal expansion of populations. They also discuss how the original MLST schemes may not have included the best genes for all bacterial species as the genes were chosen before genome sequencing became widely available. Ed and Natacha further elaborate on the concept of clonality among bacterial species. Ed suggests that bacterial population structures have no consistent pattern, with some organisms being well-behaved, while others have a lot of allele shuffling. However, clones have existed since day one, and their presence is still seen today. Natacha adds that although MLST has flaws, it leaves behind the nomenclature for the lineages or clones, which is a lasting legacy. Nabil-Fareed notes that while most reference labs have moved on to genomics, some people still use MLST. He adds that the pipeline is the same for any organism, and the process is efficient in the end. The discussion concludes with the hosts thanking the guests and promising more exciting topics in their next episode. Overall, the hosts highlight the significance of understanding the limitations of MLST and the scope for further research in bacterial population genetics.
  continue reading

139 에피소드

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