Evidence map›Paper›PMID 20587504›Full record

ArticleNucleic acids research2010

Single molecule analysis of combinatorial splicing.

Tim Conze, Jenny Göransson, Hamid Reza Razzaghian, Olle Ericsson, Daniel Oberg, Göran Akusjärvi, Ulf Landegren, Mats Nilsson

Abstract read
In one paragraph

Article in Nucleic acids research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. RNA velocity unraveled.PLoS computational biology · 2022
    Article
  2. The determinants of alternative RNA splicing in human cells.Molecular genetics and genomics : MGG · 2017
    Review
  3. Simultaneous Single-CellJournal of virology · 2017
    Article
  4. Article
  5. Article
  6. Article
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

8 authors.

Tim ConzeDepartment of Genetics and Pathology, The Rudbeck Laboratory, Uppsala University, SE-75185, Sweden. tim.conze@genpat.uu.se
Jenny Göransson
Hamid Reza Razzaghian
Olle Ericsson
Daniel Oberg
Göran Akusjärvi
Ulf Landegren
Mats Nilsson

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alternative splicing creates diverse mRNA isoforms from single genes and thereby enhances complexity of transcript structure and of gene function. We describe a method called spliceotyping, which translates combinatorial mRNA splicing patterns along transcripts into a library of binary strings of nucleic acid tags that encode the exon composition of individual mRNA molecules. The exon inclusion pattern of each analyzed transcript is thus represented as binary data, and the abundance of different splice variants is registered by counts of individual molecules. The technique is illustrated in a model experiment by analyzing the splicing patterns of the adenovirus early 1A gene and the beta actin reference transcript. The method permits many genes to be analyzed in parallel and it will be valuable for elucidating the complex effects of combinatorial splicing.

Indexed as

Alternative SplicingAdenoviridaeAdenovirus E1A ProteinsDNA ProbesHeLa CellsHumansNucleic Acid HybridizationRNA Splice SitesAdenovirus E1A ProteinsDNA ProbesRNA Splice Sites

Identifiers

PMID20587504
PMCPMC2938221

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.