Evidence map›Paper›PMID 26519169›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2016

Preprocessing and Analysis of LC-MS-Based Proteomic Data.

Tsung-Heng Tsai, Minkun Wang, Habtom W Ressom

Abstract read
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Tsung-Heng TsaiDepartment of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, DC, 20057, USA. thtsai@vt.edu.
Minkun WangDepartment of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, DC, 20057, USA.
Habtom W RessomDepartment of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, DC, 20057, USA.

Funding

Analysis of LC-MS data to identify peptide and glycan biomarkers for hepatocellulR01CA143420 · NCI · GEORGETOWN UNIVERSITY · PI RESSOM, HABTOM W · 2010 to 2014
$1.4M
Quantitative analysis of LC-MS data for peptide and glycan biomarker discoveryR01GM086746 · NIGMS · GEORGETOWN UNIVERSITY · PI RESSOM, HABTOM W · 2010 to 2014
$1.3M
NCI NIH HHS R01 CA143420NCI NIH HHS R01CA143420NIGMS NIH HHS R01 GM086746NIGMS NIH HHS R01GM086746
6 · The paper itself

Abstract

Liquid chromatography coupled with mass spectrometry (LC-MS) has been widely used for profiling protein expression levels. This chapter is focused on LC-MS data preprocessing, which is a crucial step in the analysis of LC-MS based proteomics. We provide a high-level overview, highlight associated challenges, and present a step-by-step example for analysis of data from LC-MS based untargeted proteomic study. Furthermore, key procedures and relevant issues with the subsequent analysis by multiple reaction monitoring (MRM) are discussed.

Indexed as

ProteomeChromatography, LiquidData Interpretation, StatisticalElectronic Data ProcessingMass SpectrometryProteomicsProteomeData preprocessingLabel-freeLiquid chromatography-mass spectrometry (LC-MS)Multiple reaction monitoring (MRM )Proteomics

Identifiers

PMID26519169
PMCPMC4838194

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.