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Record W2105696555 · doi:10.1074/mcp.r500005-mcp200

Statistical and Computational Methods for Comparative Proteomic Profiling Using Liquid Chromatography-Tandem Mass Spectrometry

2005· review· en· W2105696555 on OpenAlex

Why this work is in the frame

A frame that forgets how it found something cannot be audited. These are the routes that admitted this work.

affAt least one author lists a Canadian institution in the pinned OpenAlex snapshot.

Bibliographic record

VenueMolecular & Cellular Proteomics · 2005
Typereview
Languageen
FieldChemistry
TopicAdvanced Proteomics Techniques and Applications
Canadian institutionsUniversity of Toronto
Fundersnot available
KeywordsComputer scienceBiomarker discoveryProfiling (computer programming)Normalization (sociology)Data miningProteomicsComputational biologyChemistryBiology

Abstract

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The combined method of LC-MS/MS is increasingly being used to explore differences in the proteomic composition of complex biological systems. The reliability and utility of such comparative protein expression profiling studies is critically dependent on an accurate and rigorous assessment of quantitative changes in the relative abundance of the myriad of proteins typically present in a biological sample such as blood or tissue. In this review, we provide an overview of key statistical and computational issues relevant to bottom-up shotgun global proteomic analysis, with an emphasis on methods that can be applied to improve the dependability of biological inferences drawn from large proteomic datasets. Focusing on a start-to-finish approach, we address the following topics: 1) low-level data processing steps, such as formation of a data matrix, filtering, and baseline subtraction to minimize noise, 2) mid-level processing steps, such as data normalization, alignment in time, peak detection, peak quantification, peak matching, and error to processing such as sample and and such as and of on that steps, and and of The combined method of LC-MS/MS is increasingly being used to explore differences in the proteomic composition of complex biological systems. The reliability and utility of such comparative protein expression profiling studies is critically dependent on an accurate and rigorous assessment of quantitative changes in the relative abundance of the myriad of proteins typically present in a biological sample such as blood or tissue. In this review, we provide an overview of key statistical and computational issues relevant to bottom-up shotgun global proteomic analysis, with an emphasis on methods that can be applied to improve the dependability of biological inferences drawn from large proteomic datasets. Focusing on a start-to-finish approach, we address the following topics: 1) low-level data processing steps, such as formation of a data matrix, filtering, and baseline subtraction to minimize noise, 2) mid-level processing steps, such as data normalization, alignment in time, peak detection, peak quantification, peak matching, and error to processing such as sample and and such as and of on that steps, and and of the of the and emphasis in is from and a of the myriad of to the biological that and in to biological studies the of and such as protein and statistical and methods large datasets. and of data and of The of expression to the following 1) proteins and the of an 2) in of in and and and and can of this to the biological as as the of as to improve and the data and of proteomic data from of the the of biological as from to to the protein the is that of the to and in to to and that proteins typically as of the of a biological is the and relevant proteomic a is as a method of proteomic the data and to The in can be used to and the relative abundance of of expression profiling shotgun bottom-up profiling the in of complex protein such as the to the as to a of the as as of of to the of the of peak can be used to the relative of the proteins of proteomic to a of such as noise, the and of protein and the of protein of to the of In this review, we computational and statistical that be comparative proteomic and processing data to quantitative the of statistical and methods the of this review, we to studies methods to shotgun profiling datasets. statistical a is The of an of the of and the relative of the is to present in this 1) a on or to 2) an or on the of and a the relative abundance of In in and in an used and from is to or In a the the of on with a of and to the is to complex biological 1) with the to be the time, and 2) with to or used in profiling studies is of in of proteins in proteomic of such as or of proteomic in to as a and a and The of profiling studies is the and or with with expression profiling shotgun of the sample is to the sample the protein and of a of biological is an of in to a profiling is the with to the of and of relative protein abundance in shotgun is to in a sample in a In the of a comparative profiling of such as profiling can of the with a of be a a global of and the of time, to In this the be is and expression can be the data and such an is a of 1) the to be to in 2) be of the to and that is or and differences in sample to the to address the following to be 1) alignment the that 2) as to improve the methods from of and to data and as to in peak and and be to and in and to and to to In the approach, and and to the to data is to a processing with peak and to the data be as a matrix, the of methods in and The of and to and relevant from the of the such as and and in relevant to this the data and of proteins and or global proteomic profiling and to address the The of global proteomic profiling and filtering, normalization, peak detection, and and in peak with and the data and a and data the time, and of the of proteins and or baseline peak detection, detection, and and a peak to in a complex a large studies of on data processing such as error the of the or alignment in time, studies to the of sample studies to the of a from typically a of as in in a from the The in be as to the the or peak detection, or of that that from The in on to alignment can be on the or peak detection, be to this and peak can the be to and be to of as in the used peak of peak and abundance the to the alignment of in of processing of and and in and in a low-level processing mid-level processing such as and subtraction low-level In processing is applied to data that in with or statistical such as of The of methods processing data and is in to data can be as a of of the and mid-level processing methods to as a to the of sample or and In the from an of a of and is a such that the is an of the data can be a with and in the the relative abundance of and formation to a matrix, can be and typically to a to is to the in or be large to the and that the this on the global proteomic profiling and to to the with the of the used in and of proteins and or protein of used of to the of In a of data proteomic of as a of the and and with In from protein peak to be in and methods the of to this is to and noise, with in the method and from and method in methods and is a from a of The of processing is on the that data is the be is to and baseline subtraction can be in the and applied to a baseline and to and the In is and a baseline is of proteins and or data the in and and the a to the data a The and baseline the to data of proteins and or to the baseline with a and from the with a of the peak of is a and and with that the of filtering, this the of the is with a and is to of a as is on data the in and baseline and alignment of in from the that the of the is the to with filtering, to the to the global proteomic profiling and a of a is used to the peak a to the or of as being with the of the to be of of the of is to the processing of or and peak of proteins and or of an to the baseline in datasets. of in of the of the and from of the of with to with In a baseline in of an to the of of from The of a data and a of this this the baseline with a and the a baseline in is applied to from a in the to of The the and is the of the data that in this such a is is in a global in this and to the of data on a peak in The of and the of a in of the of subtraction on data and is to the on peak the to on data be to in and or is In be to and in as to or global proteomic a from the of the can analysis, and to data of this used an to and from data global proteomic profiling and in the data to be on combined to the and of the with a method used to peak the on in and as an in abundance a a of proteins and or the or on the peak the the used in protein of and processing and peak in protein of proteomic data as the 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to of of peak methods and of proteins and or global proteomic profiling and relevant to proteomic the on the and in with the in a of and with the sample is is to on of from the of of and of with to the this of the of a is on the the peak on the can the of and applied a peak of proteins and or protein of the on the peak to with the the can that such as improve this In to data the as a to from protein peak complex to be to is relevant to quantitative proteomic of be datasets. on or to be of proteins and or protein of from used to the of global proteomic profiling and that this assessment is protein of on the to of data to be to protein of of of peak and a improve the of peak detection, quantification, and the of with is typically is in can in differences in to changes in and and is in an peak can peak and global proteomic to the of to with the in the or In the as this is of a in and can be or the in the and be applied peak in to the from the data as a of or such as a as typically a of or 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Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.001
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesMeta-epidemiology (narrow)
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: Bench or experimental
GenreCandidate signal: Methods · Consensus signal: Methods
Teacher disagreement score0.164
Threshold uncertainty score0.999

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0010.000
Meta-epidemiology (narrow)0.0010.001
Meta-epidemiology (broad)0.0020.001
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0010.000
Research integrity0.0010.001
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.054
GPT teacher head0.406
Teacher spread0.352 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it