Evidence map›Paper›PMID 33959753›Full record

ArticleBriefings in bioinformatics2021

Anti-bias training for (sc)RNA-seq: experimental and computational approaches to improve precision.

Philip Davies, Matt Jones, Juntai Liu, Daniel Hebenstreit

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

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  5. Machine learning-optimized targeted detection of alternative splicing.bioRxiv : the preprint server for biology · 2024
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  7. Review
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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

4 authors.

Philip DaviesDaniel Hebenstreit's Research Group University of Warwick, CV4 7AL Coventry, UK.
Matt JonesDaniel Hebenstreit's Research Group University of Warwick, CV4 7AL Coventry, UK.
Juntai LiuPhysics Department, University of Warwick, CV4 7AL Coventry, UK.
Daniel HebenstreitUniversity of Warwick, CV4 7AL Coventry, UK.

Funding

BBSRC BB/M01116X/1Biotechnology and Biological Sciences Research Council BB/L006340/1Biotechnology and Biological Sciences Research Council BB/M017982/1
6 · The paper itself

Abstract

RNA-seq, including single cell RNA-seq (scRNA-seq), is plagued by insufficient sensitivity and lack of precision. As a result, the full potential of (sc)RNA-seq is limited. Major factors in this respect are the presence of global bias in most datasets, which affects detection and quantitation of RNA in a length-dependent fashion. In particular, scRNA-seq is affected by technical noise and a high rate of dropouts, where the vast majority of original transcripts is not converted into sequencing reads. We discuss these biases origins and implications, bioinformatics approaches to correct for them, and how biases can be exploited to infer characteristics of the sample preparation process, which in turn can be used to improve library preparation.

Indexed as

Gene LibraryRNA-SeqSoftwareComputational BiologyRNARNAbiasgene expressionmodelingquantitationRNA-seqsoftware

Identifiers

PMID33959753
PMCPMC8574610

What OpenQuestion holds

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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.