Only a small fraction of spectra acquired in LC-MS/MS runs matches peptides from target proteins upon database searches. The remaining, operationally termed background, spectra originate from a variety of poorly controlled sources and affect the throughput and confidence of database searches. Here, we report an algorithm and its software implementation that rapidly removes background spectra, regardless of their precise origin. The method estimates the dissimilarity distance between screened MS/MS spectra and unannotated spectra from a partially redundant background library compiled from several control and blank runs. Filtering MS/MS queries enhanced the protein identification capacity when searches lacked spectrum to sequence matching spe...
Peptide tandem mass spectrometry has emerged as a key technology to detect and measure proteins in b...
Abstract Motivation: Identification of proteins by mass spectrometry–based proteomics...
Liquid chromatography coupled with tandem mass spectrometry (LC–MS/MS) has revolutionized the proteo...
Only a small fraction of spectra acquired in LC-MS/MS runs matches peptides from target proteins upo...
Protein identification has been more helpful than before in the diagnosis and treatment of many dise...
Tandem mass spectrometry (MS/MS) is a powerful tool for identifying peptide sequences. In a typical ...
Motivation: Peptide identification by tandem mass spectrometry is an important tool in proteomic res...
In contemporary peptide-centric or non-gel proteome studies, vast amounts of peptide fragmentation d...
Abstract. Advances in tandem mass-spectrometry (MS/MS) steadily increase the rate of generation of M...
Background: In proteomics experiments, database-search programs are the method of choice for protei...
Several approaches exist for the quantification of proteins in complex samples processed by liquid c...
Background: The identification of proteins based on analysis of tandem mass spectrometry (MS/MS) dat...
The use of tandem mass spectrometry (MS/MS) is a well established method to identify and characteriz...
Shotgun proteomics is a widely known technique for identification of protein and peptide sequences f...
Time-consuming and experience-dependent manual vali-dations of tandem mass spectra are usually appli...
Peptide tandem mass spectrometry has emerged as a key technology to detect and measure proteins in b...
Abstract Motivation: Identification of proteins by mass spectrometry–based proteomics...
Liquid chromatography coupled with tandem mass spectrometry (LC–MS/MS) has revolutionized the proteo...
Only a small fraction of spectra acquired in LC-MS/MS runs matches peptides from target proteins upo...
Protein identification has been more helpful than before in the diagnosis and treatment of many dise...
Tandem mass spectrometry (MS/MS) is a powerful tool for identifying peptide sequences. In a typical ...
Motivation: Peptide identification by tandem mass spectrometry is an important tool in proteomic res...
In contemporary peptide-centric or non-gel proteome studies, vast amounts of peptide fragmentation d...
Abstract. Advances in tandem mass-spectrometry (MS/MS) steadily increase the rate of generation of M...
Background: In proteomics experiments, database-search programs are the method of choice for protei...
Several approaches exist for the quantification of proteins in complex samples processed by liquid c...
Background: The identification of proteins based on analysis of tandem mass spectrometry (MS/MS) dat...
The use of tandem mass spectrometry (MS/MS) is a well established method to identify and characteriz...
Shotgun proteomics is a widely known technique for identification of protein and peptide sequences f...
Time-consuming and experience-dependent manual vali-dations of tandem mass spectra are usually appli...
Peptide tandem mass spectrometry has emerged as a key technology to detect and measure proteins in b...
Abstract Motivation: Identification of proteins by mass spectrometry–based proteomics...
Liquid chromatography coupled with tandem mass spectrometry (LC–MS/MS) has revolutionized the proteo...