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National Institute of Standards and Technology human ion trap spectral library november 29, 2011 version
Precursor charge segregation events observed for NIST-CID peptides PSMs in the NIST <t>human</t> <t>ion</t> <t>trap</t> <t>spectral</t> <t>library</t> were segregated by charge state. Charge states of the observed N- and C-terminal fragments were assessed for all peptide bonds. Frequencies of precursor charge segregation events are summarized here. Label “others” include all ordinal categories which are less than 5% and any other fragment patterns that did not fit a category.
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Precursor charge segregation events observed for NIST-CID peptides PSMs in the NIST human ion trap spectral library were segregated by charge state. Charge states of the observed N- and C-terminal fragments were assessed for all peptide bonds. Frequencies of precursor charge segregation events are summarized here. Label “others” include all ordinal categories which are less than 5% and any other fragment patterns that did not fit a category.

Journal: Genomics, Proteomics & Bioinformatics

Article Title: Basophile: Accurate Fragment Charge State Prediction Improves Peptide Identification Rates

doi: 10.1016/j.gpb.2012.11.004

Figure Lengend Snippet: Precursor charge segregation events observed for NIST-CID peptides PSMs in the NIST human ion trap spectral library were segregated by charge state. Charge states of the observed N- and C-terminal fragments were assessed for all peptide bonds. Frequencies of precursor charge segregation events are summarized here. Label “others” include all ordinal categories which are less than 5% and any other fragment patterns that did not fit a category.

Article Snippet: For this dataset, we used the November 29, 2011 version of the human ion trap spectral library from the National Institute of Standards and Technology (NIST).

Techniques: