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LC MS MS Methods — DDA DIA PRM SRM Training | Acquisition Strategies for Proteomics

NTHRYS >> Services >> Academic Services >> Training Programs >> Bioinformatics Training >> Proteomics, Mass Spectrometry & PTM Analytics >> LC MS MS Methods — DDA DIA PRM SRM Training | Acquisition Strategies for Proteomics

LC MS MS Methods — DDA DIA PRM SRM — Hands-on

Develop an intuitive understanding of the major LC–MS/MS acquisition strategies used in proteomics. This module focuses on how DDA, DIA, PRM and SRM work at a conceptual level, how method parameters influence coverage, sensitivity and throughput, and how to choose and plan acquisition modes for discovery and targeted studies.

LC MS MS Methods — DDA DIA PRM SRM
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Session 1
Fee: Rs 8800
LC MS MS Fundamentals & Scan Logic
  • Signal path and key terms in LC–MS/MS
  • MS1 and MS2 precursor and fragment ions scan events and cycles
  • Chromatography and mass spectrometry together
  • retention time and peak shape gradient overview resolution vs run time
  • Cycle time, duty cycle and trade offs
  • points across a peak coverage vs sensitivity throughput considerations
Session 2
Fee: Rs 11800
DDA Methods & Optimization Concepts
  • DDA precursor selection logic
  • intensity based top N view isolation window concept charge state preferences
  • Dynamic exclusion and sampling the chromatogram
  • repeat sequencing avoidance exclusion windows complex vs simple samples
  • Using pilot runs to refine DDA methods
  • adjusting gradients mass range choices cycle settings sanity checks
Session 3
Fee: Rs 14800
DIA & PRM Design Logic
  • DIA acquisition concepts
  • segmented mass window view coverage vs interference library based vs library free ideas
  • PRM for targeted quant conceptually
  • monitoring selected precursors high resolution MS2 focus panel size and cycle time
  • When to choose DDA vs DIA vs PRM
  • discovery vs verification cohort size and depth needs instrument and time constraints
Session 4
Fee: Rs 18800
SRM Panels & Method Planning
  • SRM concept for highly targeted assays
  • theory plus planning exercise
  • Transitions, scheduling and dwell time logic
  • precursor and fragment choice time window scheduling panel size vs data quality
  • Designing a simple acquisition plan across modes
  • linking study goals to modes instrument time budgeting documenting method settings


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