OM DENNE EPISODE
The Bioinformatics Contest is back this year, and we are back to discuss it!
This year’s contest winners Maksym Kovalchuk (1st prize) and Matt Holt (2nd prize) talk about how they approach participating in the contest and what strategies have earned them the top scores.
Timestamps and links for the individual problems:
- 00:10:36 Genotype Imputation
- 00:21:26 Causative Mutation
- 00:30:27 Superspreaders
- 00:37:22 Minor Haplotype
- 00:46:37 Isoform Matching
Links:
If you enjoyed this episode, please consider supporting the podcast on Patreon.
Engelsk
USA
UDSKRIFT 🔗
Are you the producer of this podcast?
Add a podcast transcript
Need Audio-to-Text?
Transcribe with Listen411 in Just 60 Seconds
SØG BLANDT TIDLIGERE EPISODER
Søg efter gamle afsnit af the bioinformatics chat.
ANDRE EPISODE I DENNE PODCAST
Today on the podcast we have Tomasz Kociumaka and Dominik Kempa,
the authors of the preprint
Collapsing the Hierarchy of Compressed Data Structures: Suffix Arrays in Optimal Compressed Space.
The suffix array is one of the foundational data structures in bioinformatics,
serving as an index that a…
This is the third and final episode in the AlphaFold series, originally recorded on February 23, 2022,
with Amelie Stein, now an associate professor at the University of Copenhagen.
In the episode, Amelie explains what 𝛥𝛥G is, how it informs us
whether a particular protein mutation affects its st…
In this episode, Marie Sadler talks
about her recent Cell Genomics paper, Multi-layered genetic approaches to
identify approved drug targets.
Previous studies have found that the drugs that target a gene linked to the
disease are more likely to be approved. Yet there are many ways to define what
…
This is the second episode in the AlphaFold series, originally recorded on February 14, 2022,
with Janani Durairaj, a postdoctoral
researcher at the University of Basel.
Janani talks about how she used shape-mers and topic modelling to discover
classes of proteins assembled by AlphaFold 2 that we…
In this episode,
David Dylus talks about
Read2Tree,
a tool that builds alignment matrices and phylogenetic trees from raw
sequencing reads.
By leveraging the database of orthologous genes called OMA, Read2Tree bypasses traditional, time-consuming steps such as genome assembly, annotation and all-ve…
Ansvarsfraskrivelse: Podcasten og kunstværket, der er indlejret på denne side, er fra Roman Cheplyaka, som tilhører dens ejer og ikke er tilknyttet eller godkendt af Listen Notes, Inc.
REDIG
Tak fordi du hjælper med at holde podcast-databasen opdateret.
