Evidence map›Paper›PMID 35041494›Full record

ArticleJournal of computational biology : a journal of computational molecular cell biology2022

Deriving Ranges of Optimal Estimated Transcript Expression due to Nonidentifiability.

Hongyu Zheng, Cong Ma, Carl Kingsford

Abstract read
In one paragraph

Article in Journal of computational biology : a journal of computational molecular cell biology, 2022. 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

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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. Improving RNA Assembly via Safety and Completeness in Flow Decompositions.Journal of computational biology : a journal of computational molecular cell biology · 2022
    Article
  4. Efficient Minimum Flow Decomposition via Integer Linear Programming.Journal of computational biology : a journal of computational molecular cell biology · 2022
    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.

Hongyu ZhengComputational Biology Department, Carnegie Mellon University, Pittsburgh, Pennsylvania, USA.ORCID 0000-0002-7668-2090
Cong MaComputer Science Department, Princeton University, Princeton, New Jersey, USA.
Carl KingsfordComputational Biology Department, Carnegie Mellon University, Pittsburgh, Pennsylvania, USA.

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
NIGMS NIH HHS R01 GM122935
6 · The paper itself

Abstract

Current expression quantification methods suffer from a fundamental but undercharacterized type of error: the most likely estimates for transcript abundances are not unique. This means multiple estimates of transcript abundances generate the observed RNA-seq reads with equal likelihood, and the underlying true expression cannot be determined. This is called nonidentifiability in probabilistic modeling. It is further exacerbated by incomplete reference transcriptomes where reads may be sequenced from unannotated transcripts. Graph quantification is a generalization to transcript quantification, accounting for the reference incompleteness by allowing exponentially many unannotated transcripts to express reads. We propose methods to calculate a "confidence range of expression" for each transcript, representing its possible abundance across equally optimal estimates for both quantification models. This range informs both whether a transcript has potential estimation error due to nonidentifiability and the extent of the error. Applying our methods to the Human Body Map data, we observe that 35%-50% of transcripts potentially suffer from inaccurate quantification caused by nonidentifiability. When comparing the expression between isoforms in one sample, we find that the degree of inaccuracy of 20%-47% transcripts can be so large that the ranking of expression between the transcript and other isoforms from the same gene cannot be determined. When comparing the expression of a transcript between two groups of RNA-seq samples in differential expression analysis, we observe that the majority of detected differentially expressed transcripts are reliable with a few exceptions after considering the ranges of the optimal expression estimates.

Indexed as

AlgorithmsTranscriptomeAlternative SplicingComputational BiologyConfidence IntervalsDatabases, Nucleic AcidGene Expression ProfilingHumansModels, StatisticalRNA-Seqalternative splicingexpression quantificationnonidentifiability and differential expressionuncertainty

Identifiers

PMID35041494
PMCPMC8892959

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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.