Evidence map›Paper›PMID 38783092›Full record

ArticleCommunications biology2024

Pan-cancer discovery of somatic mutations from RNA sequencing data.

Gongyu Tang, Xinyi Liu, Minsu Cho, Yuanxiang Li, Dan-Ho Tran, Xiaowei Wang

Abstract read
In one paragraph

Article in Communications biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 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.

Gongyu TangDepartment of Pharmacology and Regenerative Medicine, University of Illinois at Chicago, Chicago, IL, USA.
Xinyi LiuDepartment of Pharmacology and Regenerative Medicine, University of Illinois at Chicago, Chicago, IL, USA.
Minsu ChoDepartment of Pharmacology and Regenerative Medicine, University of Illinois at Chicago, Chicago, IL, USA.
Yuanxiang LiDepartment of Pharmacology and Regenerative Medicine, University of Illinois at Chicago, Chicago, IL, USA.ORCID 0000-0001-5893-5683
Dan-Ho TranDepartment of Pharmacology and Regenerative Medicine, University of Illinois at Chicago, Chicago, IL, USA.
Xiaowei WangDepartment of Pharmacology and Regenerative Medicine, University of Illinois at Chicago, Chicago, IL, USA. xwang317@uic.edu.ORCID 0000-0001-9447-4685

Funding

MICRORNA BIOMARKERS FOR OROPHARYNGEAL CANCERR01DE026471 · NIDCR · WASHINGTON UNIVERSITY · PI WANG, XIAOWEI · 2017 to 2021
$2.2M
Combined Computational and Experimental Analyses of Gene Regulation by MicroRNAsR35GM141535 · NIGMS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI WANG, XIAOWEI · 2021 to 2025
$2.1M
Combined Imaging and RNA Analyses to Predict Head and Neck Cancer RecurrenceR56DE033344 · NIDCR · WASHINGTON UNIVERSITY · PI LI, HUA, WANG, XIAOWEI · 2023 to 2023
$673k
NIDCR NIH HHS R01 DE026471NIDCR NIH HHS R56 DE033344NIGMS NIH HHS R35 GM141535U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01DE026471, R56DE033344 and R35GM141535
6 · The paper itself

Abstract

Identification of somatic mutations (SMs) is essential for characterizing cancer genomes. While DNA-seq is the prevalent method for identifying SMs, RNA-seq provides an alternative strategy to discover tumor mutations in the transcribed genome. Here, we have developed a machine learning based pipeline to discover SMs based on RNA-seq data (designated as RNA-SMs). Subsequently, we have conducted a pan-cancer analysis to systematically identify RNA-SMs from over 8,000 tumors in The Cancer Genome Atlas (TCGA). In this way, we have identified over 105,000 novel SMs that had not been reported in previous TCGA studies. These novel SMs have significant clinical implications in designing targeted therapy for improved patient outcomes. Further, we have combined the SMs identified by both RNA-seq and DNA-seq analyses to depict an updated mutational landscape across 32 cancer types. This new online SM atlas, OncoDB ( https://oncodb.org ), offers a more complete view of gene mutations that underline the development and progression of various cancers.

Indexed as

MutationNeoplasmsDatabases, GeneticHumansMachine LearningRNA-SeqSequence Analysis, RNA

Identifiers

PMID38783092
PMCPMC11116503

What OpenQuestion holds

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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.