Evidence map›Paper›PMID 37338536›Full record

ArticleBioinformatics (Oxford, England)2023

BBmix: a Bayesian beta-binomial mixture model for accurate genotyping from RNA-sequencing.

Elena Vigorito, Anne Barton, Costantino Pitzalis, Myles J Lewis, Chris Wallace

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Genotype prediction of 336,463 samples from public expression data.bioRxiv : the preprint server for biology · 2024
    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

5 authors.

Elena VigoritoMRC Biostatistics Unit, University of Cambridge, Cambridge CB2 0SR, United Kingdom.ORCID 0000-0001-6230-3849
Anne BartonDivision of Musculoskeletal and Dermatological Sciences, University of Manchester, Manchester M13 9PL, United Kingdom.ORCID 0000-0003-3316-2527
Costantino PitzalisCentre for Experimental Medicine and Rheumatology, William Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London EC1M 6BQ, United Kingdom.
Myles J LewisCentre for Experimental Medicine and Rheumatology, William Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London EC1M 6BQ, United Kingdom.ORCID 0000-0001-9365-5345
Chris WallaceMRC Biostatistics Unit, University of Cambridge, Cambridge CB2 0SR, United Kingdom.ORCID 0000-0001-9755-1703

Funding

Arthritis Research UKDepartment of Health BRC-1215-20014Medical Research Council G0800648Medical Research Council MC_UU_ 00002/4Medical Research Council MC_UU_00002/4Medical Research Council MR-K015346Medical Research Council MR/K015346/1Wellcome TrustWellcome Trust WT220788
6 · The paper itself

Abstract

motivationWhile many pipelines have been developed for calling genotypes using RNA-sequencing (RNA-Seq) data, they all have adapted DNA genotype callers that do not model biases specific to RNA-Seq such as allele-specific expression (ASE).

resultsHere, we present Bayesian beta-binomial mixture model (BBmix), a Bayesian beta-binomial mixture model that first learns the expected distribution of read counts for each genotype, and then deploys those learned parameters to call genotypes probabilistically. We benchmarked our model on a wide variety of datasets and showed that our method generally performed better than competitors, mainly due to an increase of up to 1.4% in the accuracy of heterozygous calls, which may have a big impact in reducing false positive rate in applications sensitive to genotyping error such as ASE. Moreover, BBmix can be easily incorporated into standard pipelines for calling genotypes. We further show that parameters are generally transferable within datasets, such that a single learning run of less than 1 h is sufficient to call genotypes in a large number of samples. AVAILABILITY AND IMPLEMENTATION: We implemented BBmix as an R package that is available for free under a GPL-2 licence at https://gitlab.com/evigorito/bbmix and https://cran.r-project.org/package=bbmix with accompanying pipeline at https://gitlab.com/evigorito/bbmix_pipeline.

Indexed as

High-Throughput Nucleotide SequencingRNABayes TheoremGenotypeSequence Analysis, RNASoftwareRNA

Identifiers

PMID37338536
PMCPMC10318392

What Socratic 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 Socratic graph.