Evidence map›Paper›PMID 38720247›Full record

ArticleBMC bioinformatics2024

A comparison of RNA-Seq data preprocessing pipelines for transcriptomic predictions across independent studies.

Richard Van, Daniel Alvarez, Travis Mize, Sravani Gannavarapu, Lohitha Chintham Reddy, Fatma Nasoz, Mira V Han

Abstract readComparative Study
In one paragraph

Article in BMC bioinformatics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
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

7 authors.

Richard VanSchool of Life Sciences, University of Nevada Las Vegas, Las Vegas, NV, USA.
Daniel AlvarezDepartment of Computer Science, University of Nevada Las Vegas, Las Vegas, NV, USA.
Travis MizeIcahn School of Medicine at Mount Sinai, Institute for Genomic Health, New York City, NY, USA.
Sravani GannavarapuDepartment of Computer Science, University of Nevada Las Vegas, Las Vegas, NV, USA.
Lohitha Chintham ReddyDepartment of Computer Science, University of Nevada Las Vegas, Las Vegas, NV, USA.
Fatma NasozDepartment of Computer Science, University of Nevada Las Vegas, Las Vegas, NV, USA.
Mira V HanSchool of Life Sciences, University of Nevada Las Vegas, Las Vegas, NV, USA. mira.han@unlv.edu.

Funding

The Genome Analysis and Sequencing Pipeline (GASP)P20GM121325 · NIGMS · UNIVERSITY OF NEVADA LAS VEGAS · PI GUHA, PRASUN · 2018 to 2022
$11.5M
NIGMS NIH HHS P20 GM121325
6 · The paper itself

Abstract

backgroundRNA sequencing combined with machine learning techniques has provided a modern approach to the molecular classification of cancer. Class predictors, reflecting the disease class, can be constructed for known tissue types using the gene expression measurements extracted from cancer patients. One challenge of current cancer predictors is that they often have suboptimal performance estimates when integrating molecular datasets generated from different labs. Often, the quality of the data is variable, procured differently, and contains unwanted noise hampering the ability of a predictive model to extract useful information. Data preprocessing methods can be applied in attempts to reduce these systematic variations and harmonize the datasets before they are used to build a machine learning model for resolving tissue of origins.

resultsWe aimed to investigate the impact of data preprocessing steps-focusing on normalization, batch effect correction, and data scaling-through trial and comparison. Our goal was to improve the cross-study predictions of tissue of origin for common cancers on large-scale RNA-Seq datasets derived from thousands of patients and over a dozen tumor types. The results showed that the choice of data preprocessing operations affected the performance of the associated classifier models constructed for tissue of origin predictions in cancer.

conclusionBy using TCGA as a training set and applying data preprocessing methods, we demonstrated that batch effect correction improved performance measured by weighted F1-score in resolving tissue of origin against an independent GTEx test dataset. On the other hand, the use of data preprocessing operations worsened classification performance when the independent test dataset was aggregated from separate studies in ICGC and GEO. Therefore, based on our findings with these publicly available large-scale RNA-Seq datasets, the application of data preprocessing techniques to a machine learning pipeline is not always appropriate.

Indexed as

Machine LearningNeoplasmsRNA-SeqComputational BiologyGene Expression ProfilingHumansSequence Analysis, RNATranscriptomeBatch effect correctionCancerClassificationData scalingNormalizationRNA-Seq

Identifiers

PMID38720247
PMCPMC11080237

What OpenQuestion holds

Textmetadata
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.