Evidence map›Paper›PMID 34728536›Full record

ArticleRNA (New York, N.Y.)2022

Identification of high-confidence human poly(A) RNA isoform scaffolds using nanopore sequencing.

Logan Mulroney, Madalee G Wulf, Ira Schildkraut, George Tzertzinis, John Buswell, Miten Jain, Hugh Olsen, Mark Diekhans, Ivan R Corrêa, Mark Akeson and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in RNA (New York, N.Y.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

23 citing papers in PubMed, 28 citations in OpenAlex.

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  13. The genome of a bunyavirus cannot be defined at the level of the viral particle but only at the scale of the viral population.Proceedings of the National Academy of Sciences of the United States of America · 2023
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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 at 2 institutions in 1 country.

Logan MulroneyBiomolecular Engineering Department, UC Santa Cruz, California 95064, USA.ORCID 0000-0002-0534-0165
Madalee G WulfNew England Biolabs, Ipswich, Massachusetts 01938, USA.ORCID 0000-0002-7601-413X
Ira SchildkrautNew England Biolabs, Ipswich, Massachusetts 01938, USA.ORCID 0000-0002-1143-6630
George TzertzinisNew England Biolabs, Ipswich, Massachusetts 01938, USA.
John BuswellNew England Biolabs, Ipswich, Massachusetts 01938, USA.ORCID 0000-0002-0933-2867
Miten JainBiomolecular Engineering Department, UC Santa Cruz, California 95064, USA.ORCID 0000-0002-4571-3982
Hugh OlsenBiomolecular Engineering Department, UC Santa Cruz, California 95064, USA.ORCID 0000-0002-7293-8853
Mark DiekhansGenomics Institute, UC Santa Cruz, California 95064, USA.ORCID 0000-0002-0430-0989
Ivan R CorrêaNew England Biolabs, Ipswich, Massachusetts 01938, USA.ORCID 0000-0002-3169-6878
Mark AkesonBiomolecular Engineering Department, UC Santa Cruz, California 95064, USA.ORCID 0000-0001-9392-8075
Laurence EttwillerNew England Biolabs, Ipswich, Massachusetts 01938, USA.ORCID 0000-0002-3957-6539
New England Biolabs (United States) · USUniversity of California, Santa Cruz · US

Funding

GENCODE Resource ProjectU41HG007234 · NHGRI · SANGER INSTITUTE · PI FLICEK, PAUL · 2013 to 2020
$20.3M
GENCODE: comprehensive reference genome annotation for human and mouseU24HG007234 · NHGRI · EUROPEAN MOLECULAR BIOLOGY LABORATORY · PI Fergal James Martin · 2021 to 2026
$16.1M
Integrated human genome annotation: generation of a reference gene setU54HG004555 · NHGRI · SANGER INSTITUTE · PI HUBBARD, TIMOTHY JOHN · 2007 to 2012
$11.2M
A Unified Nanopore Platform for Direct Sequencing of Individual Full Length RNA Strands Bearing Modified NucleotidesR01HG010053 · NHGRI · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI AKESON, MARK A · 2018 to 2021
$3.8M
NHGRI NIH HHS R01 HG010053NHGRI NIH HHS U24 HG007234NHGRI NIH HHS U41 HG007234NHGRI NIH HHS U54 HG004555
6 · The paper itself

Abstract

Nanopore sequencing devices read individual RNA strands directly. This facilitates identification of exon linkages and nucleotide modifications; however, using conventional direct RNA nanopore sequencing, the 5' and 3' ends of poly(A) RNA cannot be identified unambiguously. This is due in part to RNA degradation in vivo and in vitro that can obscure transcription start and end sites. In this study, we aimed to identify individual full-length human RNA isoforms among ∼4 million nanopore poly(A)-selected RNA reads. First, to identify RNA strands bearing 5' m

Indexed as

Cell Line, TumorHumansNanopore SequencingRNA 3' Polyadenylation SignalsRNA IsoformsRNA, MessengerTranscriptomeRNA IsoformsRNA, Messengerdirect RNAfull-lengthnanoporeRNARNA isoformssingle-moleculetranscription start sitetranscriptomics

Identifiers

PMID34728536
PMCPMC8906549
OpenAlexW3209837036

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.