Evidence map›Paper›PMID 33971903›Full record

ArticleAlgorithms for molecular biology : AMB2021

Exact transcript quantification over splice graphs.

Cong Ma, Hongyu Zheng, Carl Kingsford

Abstract read
In one paragraph

Article in Algorithms for molecular biology : AMB, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Deriving Ranges of Optimal Estimated Transcript Expression due to Nonidentifiability.Journal of computational biology : a journal of computational molecular cell biology · 2022
    Article
  4. 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

3 authors.

Cong Ma *Computer Science Department, School of Engineering and Applied Science, Princeton University, 35 Olden Street, Princeton, NJ, 08544, USA.
Hongyu Zheng *Computational Biology Department, School of Computer Science, Carnegie Mellon University, 5000 Forbes Avenue, Pittsburgh, PA, 15213, USA.
Carl KingsfordComputational Biology Department, School of Computer Science, Carnegie Mellon University, 5000 Forbes Avenue, Pittsburgh, PA, 15213, USA. carlk@cs.cmu.edu.ORCID http://orcid.org/0000-0002-0118-5516

Funding

Data Discovery: Computational Methods for Searching Short-Read Sequencing Experiments - Administrative SupplementR01GM122935 · NIGMS · CARNEGIE-MELLON UNIVERSITY · PI KINGSFORD, CARLETON LEE · 2017 to 2021
$1.2M
Gordon and Betty Moore Foundation GBMF4554NIGMS NIH HHS R01 GM122935NIH HHS DBI-1937540NIH HHS R01GM122935Pennsylvania Department of Health 4100070287
6 · The paper itself

Abstract

backgroundThe probability of sequencing a set of RNA-seq reads can be directly modeled using the abundances of splice junctions in splice graphs instead of the abundances of a list of transcripts. We call this model graph quantification, which was first proposed by Bernard et al. (Bioinformatics 30:2447-55, 2014). The model can be viewed as a generalization of transcript expression quantification where every full path in the splice graph is a possible transcript. However, the previous graph quantification model assumes the length of single-end reads or paired-end fragments is fixed.

resultsWe provide an improvement of this model to handle variable-length reads or fragments and incorporate bias correction. We prove that our model is equivalent to running a transcript quantifier with exactly the set of all compatible transcripts. The key to our method is constructing an extension of the splice graph based on Aho-Corasick automata. The proof of equivalence is based on a novel reparameterization of the read generation model of a state-of-art transcript quantification method.

conclusionWe propose a new approach for graph quantification, which is useful for modeling scenarios where reference transcriptome is incomplete or not available and can be further used in transcriptome assembly or alternative splicing analysis.

Indexed as

Alternative splicingNetwork flowRNA-seqSplice graphTranscript quantification

Identifiers

PMID33971903
PMCPMC8112020

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.