Abstract Background The target-decoy strategy effectively estimates the false-discovery rate (FDR) by creating a decoy database with a size identical to that of the target database. Decoy databases are created by various methods, such as, the reverse, pseudo-reverse, shuffle, pseudo-shuffle, and the de Bruijn methods. FDR is sometimes over- or under-estimated depending on which decoy database is used because the ratios of redundant peptides in the target databases are different, that is, the numbers of unique (non-redundancy) peptides in the target and decoy databases differ. Results We used two protein databases (the UniProt Saccharomyces cerevisiae protein database and the UniProt human protein database) to compare the FDRs of various dec...
Abstract Background In mass spectrometry-based proteomics, protein identification is an essential ta...
Background: In high-throughput studies, hundreds to millions of hypotheses are typically tested. Sta...
Abstract Background Proteomic protein identification results need to be compared across laboratories...
(A) Among noncanonical proteins, the ratio of decoys detected to targets detected, across a range of...
International audienceIn their recent article, Madej et al. 1 proposed an original way to solve the ...
False discovery rates (FDR) for identification of proteins and peptides using decoy method by Scaffo...
In shotgun proteomics, high-throughput mass spectrom-etry experiments and the subsequent data analys...
<div><p>The statistical validation of database search results is a complex issue in bottom-up proteo...
Motivation: Statistical validation of protein identifications is an im-portant issue in shotgun prot...
The statistical validation of database search results is a complex issue in bottom-up proteomics. Th...
Abstract Automated database search engines are one of the fundamental engines of high-throughput pro...
Decoy database search with target-decoy competition (TDC) provides an intuitive, easy-to-implement m...
Tandem mass spectrometry is commonly used to identify peptides, typically by comparing their product...
Tandem mass spectrometry is commonly used to identify peptides, typically by comparing their product...
The target-decoy database search strategy is often applied to determine the global false-discovery r...
Abstract Background In mass spectrometry-based proteomics, protein identification is an essential ta...
Background: In high-throughput studies, hundreds to millions of hypotheses are typically tested. Sta...
Abstract Background Proteomic protein identification results need to be compared across laboratories...
(A) Among noncanonical proteins, the ratio of decoys detected to targets detected, across a range of...
International audienceIn their recent article, Madej et al. 1 proposed an original way to solve the ...
False discovery rates (FDR) for identification of proteins and peptides using decoy method by Scaffo...
In shotgun proteomics, high-throughput mass spectrom-etry experiments and the subsequent data analys...
<div><p>The statistical validation of database search results is a complex issue in bottom-up proteo...
Motivation: Statistical validation of protein identifications is an im-portant issue in shotgun prot...
The statistical validation of database search results is a complex issue in bottom-up proteomics. Th...
Abstract Automated database search engines are one of the fundamental engines of high-throughput pro...
Decoy database search with target-decoy competition (TDC) provides an intuitive, easy-to-implement m...
Tandem mass spectrometry is commonly used to identify peptides, typically by comparing their product...
Tandem mass spectrometry is commonly used to identify peptides, typically by comparing their product...
The target-decoy database search strategy is often applied to determine the global false-discovery r...
Abstract Background In mass spectrometry-based proteomics, protein identification is an essential ta...
Background: In high-throughput studies, hundreds to millions of hypotheses are typically tested. Sta...
Abstract Background Proteomic protein identification results need to be compared across laboratories...