Evidence map›Paper›PMID 39068368›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2024

GAN Learning Methods for Bulk RNA-Seq Data and Their Interpretive Application in the Context of Disease Progression.

Yongjin Kim, Mookyung Cheon

Abstract read
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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Yongjin KimDementia Research Group, Korea Brain Research Institute (KBRI), Daegu, Republic of Korea.
Mookyung CheonDementia Research Group, Korea Brain Research Institute (KBRI), Daegu, Republic of Korea. mkcheon@kbri.re.kr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A generative adversarial network (GAN) is a generative model that consists of two adversarial networks, a discriminator and a generator, usually in the form of neural networks. One of the useful things about applying GANs is that they can synthesize two states to produce an intermediate output that implies a semantic feature. When applied to omics data that determine phenotypes of a disease, GANs can be used to associate these intermediate outputs with the progression of the disease. In this chapter, to realize the above idea, we will introduce the application of GAN methods to bulk RNA-seq data, which cover data preprocessing, training, and latent interpolation between different phenotypes describing disease progression.

Indexed as

Disease ProgressionNeural Networks, ComputerRNA-SeqAlgorithmsComputational BiologyHumansMachine LearningSequence Analysis, RNAAlzheimer’s diseaseBulk RNA-seqDisease progressionGenerative adversarial networks (GANs)

Identifiers

PMID39068368

What OpenQuestion holds

Textmetadata
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.