Evidence map›Paper›PMID 38297116›Full record

ArticleScientific reports2024

DEEPOMICS FFPE, a deep neural network model, identifies DNA sequencing artifacts from formalin fixed paraffin embedded tissue with high accuracy.

Dong-Hyuk Heo, Inyoung Kim, Heejae Seo, Seong-Gwang Kim, Minji Kim, Jiin Park, Hongsil Park, Seungmo Kang, Juhee Kim, Soonmyung Paik and 1 more

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

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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

9 citing papers in PubMed.

  1. Review
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  6. Microbiome-Genome Crosstalk in Colorectal Cancer: Colibactin Signatures andInternational journal of molecular sciences · 2026
    Review
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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

11 authors.

Dong-Hyuk HeoTheragen Bio Co., Ltd., Seongnam, Gyeonggi-do, 13488, Republic of Korea.
Inyoung KimTheragen Bio Co., Ltd., Seongnam, Gyeonggi-do, 13488, Republic of Korea.
Heejae SeoTheragen Bio Co., Ltd., Seongnam, Gyeonggi-do, 13488, Republic of Korea.
Seong-Gwang KimTheragen Bio Co., Ltd., Seongnam, Gyeonggi-do, 13488, Republic of Korea.
Minji KimTheragen Bio Co., Ltd., Seongnam, Gyeonggi-do, 13488, Republic of Korea.
Jiin ParkTheragen Bio Co., Ltd., Seongnam, Gyeonggi-do, 13488, Republic of Korea.
Hongsil ParkTheragen Bio Co., Ltd., Seongnam, Gyeonggi-do, 13488, Republic of Korea.
Seungmo KangTheragen Bio Co., Ltd., Seongnam, Gyeonggi-do, 13488, Republic of Korea.
Juhee KimTheragen Bio Co., Ltd., Seongnam, Gyeonggi-do, 13488, Republic of Korea.
Soonmyung PaikTheragen Bio Co., Ltd., Seongnam, Gyeonggi-do, 13488, Republic of Korea.
Seong-Eui HongTheragen Bio Co., Ltd., Seongnam, Gyeonggi-do, 13488, Republic of Korea. seongeui.hong@theragenbio.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Formalin-fixed, paraffin-embedded (FFPE) tissue specimens are routinely used in pathological diagnosis, but their large number of artifactual mutations complicate the evaluation of companion diagnostics and analysis of next-generation sequencing data. Identification of variants with low allele frequencies is challenging because existing FFPE filtering tools label all low-frequency variants as artifacts. To address this problem, we aimed to develop DEEPOMICS FFPE, an AI model that can classify a true variant from an artifact. Paired whole exome sequencing data from fresh frozen and FFPE samples from 24 tumors were obtained from public sources and used as training and validation sets at a ratio of 7:3. A deep neural network model with three hidden layers was trained with input features using outputs of the MuTect2 caller. Contributing features were identified using the SHapley Additive exPlanations algorithm and optimized based on training results. The performance of the final model (DEEPOMICS FFPE) was compared with those of existing models (MuTect filter, FFPolish, and SOBDetector) by using well-defined test datasets. We found 41 discriminating properties for FFPE artifacts. Optimization of property quantification improved the model performance. DEEPOMICS FFPE removed 99.6% of artifacts while maintaining 87.1% of true variants, with an F1-score of 88.3 in the entire dataset not used for training, which is significantly higher than those of existing tools. Its performance was maintained even for low-allele-fraction variants with a specificity of 0.995, suggesting that it can be used to identify subclonal variants. Different from existing methods, DEEPOMICS FFPE identified most of the sequencing artifacts in the FFPE samples while retaining more of true variants, including those of low allele frequencies. The newly developed tool DEEPOMICS FFPE may be useful in designing capture panels for personalized circulating tumor DNA assay and identifying candidate neoepitopes for personalized vaccine design. DEEPOMICS FFPE is freely available on the web ( http://deepomics.co.kr/ffpe ) for research.

Indexed as

ArtifactsFormaldehydeHigh-Throughput Nucleotide SequencingNeural Networks, ComputerParaffin EmbeddingSequence Analysis, DNATissue FixationFormaldehyde

Identifiers

PMID38297116
PMCPMC10831091

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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.