NLM DIR Seminar Schedule
UPCOMING SEMINARS
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July 3, 2025 Matthew Diller
Using Ontologies to Make Knowledge Computable -
July 15, 2025 Noam Rotenberg
Cell phenotypes in the biomedical literature: a systematic analysis and the NLM CellLink text mining corpus
RECENT SEMINARS
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July 3, 2025 Matthew Diller
Using Ontologies to Make Knowledge Computable -
July 1, 2025 Yoshitaka Inoue
Graph-Aware Interpretable Drug Response Prediction and LLM-Driven Multi-Agent Drug-Target Interaction Prediction -
June 10, 2025 Aleksandra Foerster
Interactions at pre-bonding distances and bond formation for open p-shell atoms: a step toward biomolecular interaction modeling using electrostatics -
June 3, 2025 MG Hirsch
Interactions among subclones and immunity controls melanoma progression -
May 29, 2025 Harutyun Sahakyan
In silico evolution of globular protein folds from random sequences
Scheduled Seminars on Sept. 24, 2024
Contact NLMDIRSeminarScheduling@mail.nih.gov with questions about this seminar.
Abstract:
Accumulation of massive amount of non-targeted sequencing data allows to reverse traditional virus discovery pathway. Classically, viruses were discovered as disease agents, isolated, sequenced, and analyzed. Later, similarities between these sequences were built into virus classification and given an evolutionary perspective. Nowadays, it became possible to discover previously unknown and undetected viruses directly from (meta)genomic sequences. Annotation is heavily assisted by availability of a large amount of related virus sequences, which increase the sensitivity and reduces dependence on external libraries of known domains and functions. This also facilitates classification and evolutionary reconstruction concurrent with the discovery.
I illustrate this using the discovery of mriyaviruses (proposed class (“Mriyaviricetes”), a group of small relatives of giant viruses (Nucleocytoviricota). The most intriguing feature of “Mriyaviricetes” is their putative ancestral status with respect to previously described Nucleocytoviricota, as indicated by their deep placement in phylogenetic trees of the conserved proteins and by comparison of the major capsid protein structures. Analysis of proteins encoded in mriyavirus genomes suggests that they replicate their genome via the rolling circle mechanism that so far was not described for members of Nucleocytoviricota. Further expansion of the “Mriyaviricetes” through extended metagenome mining can be expected to further clarify and solidify the scenario for the origin and evolution of the phylum Nucleocytoviricota and viral gigantism.