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proteotypic

Prediction of the flyability of proteotypic peptides


Description

Prediction of the flyability of proteotypic peptides.

Usage

## Default S3 method:
proteotypic(fasta, apex_model, min_aa=4 , max_aa=20, ...)

Arguments

fasta

a amino acid FASTA file.

apex_model

an APEX object.

min_aa

the minimum number of amino acids for proteotypic peptides.

max_aa

the maximum number of amino acids for proteotypic peptides.

...

future extensions.

Details

This function provides prediction of the "flyability" of proteotypic peptides using the APEX method (Lu et al., 2006; Vogel et al., 2008). The APEX scores are probabilities that indicate detectability of the peptide amino acid sequence in LC-MS/MS experiments.

Value

A data.frame containing peptide sequences and associated APEX scores.

Author(s)

George Rosenberger gr2578@cumc.columbia.edu

References

Lu, P., Vogel, C., Wang, R., Yao, X. & Marcotte, E. M. Absolute protein expression profiling estimates the relative contributions of transcriptional and translational regulation. Nat Biotech 25, 117-124 (2006).

Vogel, C. & Marcotte, E. M. Calculating absolute and relative protein abundance from mass spectrometry-based protein expression data. Nat Protoc 3, 1444-1451 (2008).

See Also

Examples

set.seed(131)

data(APEXMS)

APEX_ORBI<-head(APEX_ORBI,20) # Remove this line for real applications
APEX_ORBI.af <- apexFeatures(APEX_ORBI)
APEX_ORBI.apex <- APEX(data=APEX_ORBI.af)

peptides <- proteotypic(fasta=system.file("extdata","example.fasta",package="aLFQ"),
apex_model=APEX_ORBI.apex, min_aa=4 , max_aa=20)
## Not run: print(peptides)

aLFQ

Estimating Absolute Protein Quantities from Label-Free LC-MS/MS Proteomics Data

v1.3.6
GPL (>= 3)
Authors
George Rosenberger, Hannes Roest, Christina Ludwig, Ruedi Aebersold, Lars Malmstroem
Initial release
2020-01-07

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