Oligonucleotide Fragmentation Data from Multiple Ion Activation Experiments
by Frédéric Rosu·Updated 1mo ago
960.5 KB1files
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Description
Experimental data from ion activation experiments performed on a timsOmni mass spectrometer for oligonucleotide analysis. The dataset, authored by Frédéric Rosu and last updated in April 2026, compares fragmentation results from techniques including resonance collision-induced dissociation, electron detachment dissociation, and laser photodissociation. It includes analysis of standard sequences, the therapeutic oligonucleotide Fomivirsen, and longer 46-mer DNA and RNA strands.
Use Cases
Comparing the effectiveness of different ion activation techniques (RCID, EDD, IRMPD, UVPD) based on the described experimental results.
Benchmarking sequence coverage for oligonucleotide therapeutics like Fomivirsen based on the fragmentation analysis mentioned.
Studying the generation of specific fragment ions (a•, d, z•, w) from electron detachment dissociation as described in the MS4 experiments.
Evaluating multi-stage activation combinations (e.g., EDD-RCID, EDD-IRMPD) for sequencing longer oligonucleotides based on the 46-mer analysis.
Strengths
Includes data from four distinct activation methods (RCID, EDD, IRMPD, UVPD) allowing for direct comparison.
Covers a range of oligonucleotide lengths, from a 6-mer standard to a 46-mer DNA/RNA, as stated in the description.
Demonstrates advanced multi-stage experiments (MS3, MS4) for validating fragmentation pathways.
Limitations
Column-level documentation is absent; field semantics must be inferred after download.
Row count is unknown, which may limit suitability assessment.
The dataset is small (960.5 KB), indicating a limited experimental scope.
Provenance
Source
Figshare
Collection Method
Experimental data from mass spectrometry analysis on a timsOmni platform with an integrated Omnitrap.
Time Range
null
Freshness
Last updated 2026-04-30 14:33:29; freshness should be verified.
Geography
null
License is CC-BY-NC-4.0, which prohibits commercial use.