Evidence map›Paper›PMID 37790386›Full record

ArticlebioRxiv : the preprint server for biology2023

KSHV 3.0: A State-of-the-Art Annotation of the Kaposi's Sarcoma-Associated Herpesvirus Transcriptome Using Cross-Platform Sequencing.

István Prazsák, Dóra Tombácz, Ádám Fülöp, Gábor Torma, Gábor Gulyás, Ákos Dörmő, Balázs Kakuk, Lauren McKenzie Spires, Zsolt Toth, Zsolt Boldogkői

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. 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, 2 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 2 countries.

István PrazsákDepartment of Medical Biology, Albert Szent-Györgyi Medical School, University of Szeged, Szeged, Hungary.
Dóra TombáczDepartment of Medical Biology, Albert Szent-Györgyi Medical School, University of Szeged, Szeged, Hungary.
Ádám FülöpDepartment of Medical Biology, Albert Szent-Györgyi Medical School, University of Szeged, Szeged, Hungary.
Gábor TormaDepartment of Medical Biology, Albert Szent-Györgyi Medical School, University of Szeged, Szeged, Hungary.
Gábor GulyásDepartment of Medical Biology, Albert Szent-Györgyi Medical School, University of Szeged, Szeged, Hungary.
Ákos DörmőDepartment of Medical Biology, Albert Szent-Györgyi Medical School, University of Szeged, Szeged, Hungary.
Balázs KakukDepartment of Medical Biology, Albert Szent-Györgyi Medical School, University of Szeged, Szeged, Hungary.
Lauren McKenzie SpiresDepartment of Oral Biology, University of Florida College of Dentistry, Gainesville, Florida, USA.
Zsolt TothDepartment of Oral Biology, University of Florida College of Dentistry, Gainesville, Florida, USA.
Zsolt BoldogkőiDepartment of Medical Biology, Albert Szent-Györgyi Medical School, University of Szeged, Szeged, Hungary.
University of Szeged · HUUniversity of Florida · US

Funding

Viral and host strategies for regulation of KSHV infectionR01AI132554 · NIAID · UNIVERSITY OF FLORIDA · PI TOTH, ZSOLT · 2018 to 2022
$1.9M
NIAID NIH HHS R01 AI132554
6 · The paper itself

Abstract

Kaposi's sarcoma-associated herpesvirus (KSHV) is a large, oncogenic DNA virus belonging to the gammaherpesvirus subfamily. KSHV has been extensively studied with various high-throughput RNA-sequencing approaches to map the transcription start and end sites, the splice junctions, and the translation initiation sites. Despite these efforts, the comprehensive annotation of the viral transcriptome remains incomplete. In the present study, we generated a long-read sequencing dataset of the lytic and latent KSHV transcriptome using native RNA and direct cDNA sequencing methods. This was supplemented with CAGE sequencing based on a short-read platform. We also utilized datasets from previous publications for our analysis. As a result of this combined approach, we have identified a number of novel viral transcripts and RNA isoforms and have either corroborated or improved the annotation of previously identified viral RNA molecules, thereby notably enhancing our comprehension of the transcriptomic architecture of the KSHV genome. We also evaluated the coding capability of transcripts previously thought to be non-coding, by integrating our data on the viral transcripts with translatomic information from other publications.

Indexed as

CAGEherpesvirusesKaposi’s sarcoma-associated herpesvirus (KSHV)nanopore sequencingTESTIStranscriptomeTSS

Identifiers

PMID37790386
PMCPMC10542539
OpenAlexW4386988557

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.