Proteomics

Dataset Information

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MGVB: a new proteomics toolset for fast and efficient data analysis


ABSTRACT: MGVB is a collection of tools for proteomics data analysis. It covers data processing from in silico digestion of protein sequences to comprehensive identification of postranslational modifications and solving the protein inference problem. The toolset is developed with efficiency in mind. It enables analysis at a fraction of the resources cost typically required by existing commercial and free tools. MGVB, as it is a native application, is much faster than existing proteomics tools such as MaxQuant and MSFragger and, in the same time, finds very similar, in some cases even larger number of peptides at a chosen level of statistical significance. It implements a probabilistic scoring function to match spectra to sequences, and a novel combinatorial search strategy for finding post-translational modifications, and a Bayesian approach to locate modification sites. This report describes the algorithms behind the tools, presents benchmarking data sets analysis comparing MGVB performance to MaxQuant/Andromeda, and provides step by step instructions for using it in typical analytical scenarios. The toolset is provided free to download and use for academic research and in software projects, but is not open source at the present. It is the intention of the author that it will be made open source in the near future—following rigorous evaluations and feedback from the proteomics research community.

INSTRUMENT(S): LTQ Orbitrap Velos

ORGANISM(S): Homo Sapiens (human)

TISSUE(S): Epithelial Cell

DISEASE(S): Breast Cancer

SUBMITTER: Metodi Metodiev  

LAB HEAD: Metodi V.

PROVIDER: PXD051331 | Pride | 2024-11-15

REPOSITORIES: Pride

Dataset's files

Source:
Action DRS
GFP1.raw Raw
GFP2.raw Raw
GFP3.raw Raw
WT1.raw Raw
WT2.raw Raw
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Publications

Decreased Usage of Specific Scrib Exons Defines a More Malignant Phenotype of Breast Cancer With Worsened Survival.

Metodieva Gergana G   Adoki Samson S   Lausen Berthold B   Metodiev Metodi V MV  

EBioMedicine 20160507


SCRIB is a polarity regulator known to be abnormally expressed in cancer at the protein level. Here we report that, in breast cancer, an additional and hidden dimension of deregulations exists: an unexpected SCRIB exon usage pattern appears to mark a more malignant tumor phenotype and significantly correlates with survival. Conserved exons encoding the leucine-rich repeats tend to be overexpressed while others are underused. Mechanistic studies revealed that the underused exons encode part of th  ...[more]

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