NLM DIR Seminar Schedule
UPCOMING SEMINARS
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April 8, 2025 Jaya Srivastava
Leveraging a deep learning model to assess the impact of regulatory variants on traits and diseases -
April 15, 2025 Pascal Mutz
TBD -
April 18, 2025 Valentina Boeva, Department of Computer Science, ETH Zurich
Decoding tumor heterogeneity: computational methods for scRNA-seq and spatial omics -
April 22, 2025 Stanley Liang
TBD -
April 29, 2025 MG Hirsch
TBD
RECENT SEMINARS
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April 1, 2025 Roman Kogay
Horizontal transfer of bacterial operons into eukaryote genomes -
March 25, 2025 Yifan Yang
Adversarial Manipulation and Data Memorization in Large Language Models for Medicine -
March 11, 2025 Sofya Garushyants
Tmn – bacterial anti-phage defense system -
March 4, 2025 Sanasar Babajanyan
Evolution of antivirus defense in prokaryotes depending on the environmental virus load -
Feb. 25, 2025 Zhizheng Wang
GeneAgent: Self-verification Language Agent for Gene Set Analysis using Domain Databases
Scheduled Seminars on March 31, 2023
Contact NLMDIRSeminarScheduling@mail.nih.gov with questions about this seminar.
Abstract:
Fast and accurate identification of pathogenic bacteria along with the identification of antibiotic resistance proteins is of paramount importance for patient treatments and public health. Once pathogenic bacteria causing infections are identified swiftly along with their antibiotic resistance proteins (if present), proper treatment can be administered, which can increase patients’ survival rate and minimize improper use of antibiotics. Trustworthy biomass estimates, on the other hand, are critical for microbial community structure analyses that arise in almost every microbiome study. To address these important issues, we have developed MiCId, a mass-spectrometry-based proteomics workflow for rapid identification of microorganisms and antibiotic resistance proteins and estimation of biomass.
In this talk I will demonstrate that MiCId’s workflow for pathogen identification has a sensitivity between 83.2% - 93.9% when the proportion of false discoveries controlled at the 5%. For the identification of antibiotic resistance proteins, MiCId’s workflow has a sensitivity value around 85% (with a lower bound at about 72%) and a precision greater than 95%. In addition to having high sensitivity and precision, MiCId’s workflow is fast and portable, making it a valuable tool for rapid identifications of bacteria as well as for detection of their antibiotic resistance proteins. It performs microorganismal identifications, protein identifications, sample biomass estimates, and antibiotic resistance protein identifications in 6−17 min per MS/MS experiment using computing resources that are available in most desktop and laptop computers.