Evidence map›Paper›PMID 32745614›Full record

ArticleThe Journal of molecular diagnostics : JMD2020

Genetic Characterization of Pediatric Sarcomas by Targeted RNA Sequencing.

Matthew R Avenarius, Cecelia R Miller, Michael A Arnold, Selene Koo, Ryan Roberts, Martin Hobby, Thomas Grossman, Yvonne Moyer, Richard K Wilson, Elaine R Mardis and 2 more

Open access · greenAbstract read
In one paragraph

Article in The Journal of molecular diagnostics : JMD, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.3field-weighted citation impact, top 17% of its field
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

8 citing papers in PubMed, 18 citations in OpenAlex.

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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

12 authors at 1 institution in 1 country.

Matthew R AvenariusInstitute for Genomic Medicine, Nationwide Children's Hospital, Columbus, Ohio.
Cecelia R MillerInstitute for Genomic Medicine, Nationwide Children's Hospital, Columbus, Ohio; Department of Pathology, Wexner Medical Center, The Ohio State University, Columbus, Ohio.
Michael A ArnoldDepartment of Pathology, Wexner Medical Center, The Ohio State University, Columbus, Ohio; Department of Pathology, Nationwide Children's Hospital, Columbus, Ohio.
Selene KooDepartment of Pathology, Wexner Medical Center, The Ohio State University, Columbus, Ohio; Department of Pathology, Nationwide Children's Hospital, Columbus, Ohio.
Ryan RobertsDepartment of Hematology and Oncology, Nationwide Children's Hospital, Columbus, Ohio.
Martin HobbyInstitute for Genomic Medicine, Nationwide Children's Hospital, Columbus, Ohio.
Thomas GrossmanInstitute for Genomic Medicine, Nationwide Children's Hospital, Columbus, Ohio.
Yvonne MoyerInstitute for Genomic Medicine, Nationwide Children's Hospital, Columbus, Ohio.
Richard K WilsonInstitute for Genomic Medicine, Nationwide Children's Hospital, Columbus, Ohio; Department of Pediatrics, Wexner Medical Center, The Ohio State University, Columbus, Ohio.
Elaine R MardisInstitute for Genomic Medicine, Nationwide Children's Hospital, Columbus, Ohio; Department of Pediatrics, Wexner Medical Center, The Ohio State University, Columbus, Ohio.
Julie M Gastier-FosterInstitute for Genomic Medicine, Nationwide Children's Hospital, Columbus, Ohio; Department of Pediatrics, Wexner Medical Center, The Ohio State University, Columbus, Ohio.
Ruthann B PfauInstitute for Genomic Medicine, Nationwide Children's Hospital, Columbus, Ohio; Department of Pathology, Wexner Medical Center, The Ohio State University, Columbus, Ohio. Electronic address: ruthann.pfau@nationwidechildrens.org.
Nationwide Children's Hospital · US

Funding

Elucidating and exploiting the mechanisms by which IL-6 and IL-8 facilitate osteosarcoma metastasisK08CA201638 · NCI · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI ROBERTS, RYAN D. · 2016 to 2020
$815k
NCI NIH HHS K08 CA201638
6 · The paper itself

Abstract

Somatic variants, primarily fusion genes and single-nucleotide variants (SNVs) or insertions/deletions (indels), are prevalent among sarcomas. In many cases, accurate diagnosis of these tumors incorporates genetic findings that may also carry prognostic or therapeutic significance. Using the anchored multiplex PCR-based FusionPlex system, a custom RNA sequencing panel was developed that simultaneously detects fusion genes, SNVs, and indels in 112 genes found to be recurrently mutated in solid tumors. Using this assay, a retrospective analysis was conducted to identify somatic variants that may have assisted with classifying a cohort of 90 previously uncharacterized primarily pediatric sarcoma specimens. In total, somatic variants were identified in 45.5% (41/90) of the samples tested, including 22 cases with fusion genes and 19 cases with SNVs or indels. In addition, two of these findings represent novel alterations: a WHSC1L1/NCOA2 fusion and a novel in-frame deletion in the NRAS gene (NM_002524: c.174_176delAGC p.Ala59del). These sequencing results, taken in context with the available clinical data, indicate a potential change in the initial diagnosis, prognosis, or management in 27 of the 90 cases. This study presents a custom RNA sequencing assay that detects fusion genes and SNVs in tandem and has the ability to identify novel fusion partners. These features highlight the advantages associated with utilizing anchored multiplex PCR technology for the rapid and highly sensitive detection of somatic variants.

Indexed as

Sequence Analysis, RNAChildChild, PreschoolFemaleHumansInfantInfant, NewbornMaleSarcoma

Identifiers

PMID32745614
PMCPMC7538815
OpenAlexW3046682925

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.