Evidence map›Paper›PMID 33537181›Full record

ArticleIEEE access : practical innovations, open solutions2021

Methods for Proteogenomics Data Analysis, Challenges, and Scalability Bottlenecks: A Survey.

Muhammad Usman Tariq, Muhammad Haseeb, Mohammed Aledhari, Rehma Razzak, Reza M Parizi, Fahad Saeed

Abstract read
In one paragraph

Article in IEEE access : practical innovations, open solutions, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 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

6 authors.

Muhammad Usman TariqSchool of Computing and Information Sciences, Florida International University, Miami, FL 33199, USA.
Muhammad HaseebSchool of Computing and Information Sciences, Florida International University, Miami, FL 33199, USA.ORCID 0000-0002-0697-6894
Mohammed AledhariCollege of Computing and Software Engineering, Kennesaw State University, Marietta, GA 30060, USA.ORCID 0000-0002-5380-6003
Rehma RazzakCollege of Computing and Software Engineering, Kennesaw State University, Marietta, GA 30060, USA.ORCID 0000-0002-5301-8955
Reza M PariziCollege of Computing and Software Engineering, Kennesaw State University, Marietta, GA 30060, USA.ORCID 0000-0002-0049-4296
Fahad SaeedSchool of Computing and Information Sciences, Florida International University, Miami, FL 33199, USA.ORCID 0000-0002-3410-9552

Funding

Multimodal Machine-Learning and High Performance Computing Strategies for Big MS Proteomics DataR01GM134384 · NIGMS · FLORIDA INTERNATIONAL UNIVERSITY · PI SAEED, FAHAD · 2020 to 2022
$1.3M
NIGMS NIH HHS R01 GM134384
6 · The paper itself

Abstract

Big Data Proteogenomics lies at the intersection of high-throughput Mass Spectrometry (MS) based proteomics and Next Generation Sequencing based genomics. The combined and integrated analysis of these two high-throughput technologies can help discover novel proteins using genomic, and transcriptomic data. Due to the biological significance of integrated analysis, the recent past has seen an influx of proteogenomic tools that perform various tasks, including mapping proteins to the genomic data, searching experimental MS spectra against a six-frame translation genome database, and automating the process of annotating genome sequences. To date, most of such tools have not focused on scalability issues that are inherent in proteogenomic data analysis where the size of the database is much larger than a typical protein database. These state-of-the-art tools can take more than half a month to process a small-scale dataset of one million spectra against a genome of 3 GB. In this article, we provide an up-to-date review of tools that can analyze proteogenomic datasets, providing a critical analysis of the techniques' relative merits and potential pitfalls. We also point out potential bottlenecks and recommendations that can be incorporated in the future design of these workflows to ensure scalability with the increasing size of proteogenomic data. Lastly, we make a case of how high-performance computing (HPC) solutions may be the best bet to ensure the scalability of future big data proteogenomic data analysis.

Indexed as

big datagenomicshigh-performance computingmass spectrometryProteogenomicsproteomicsworkflow

Identifiers

PMID33537181
PMCPMC7853650

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.