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Record W3087597930 · doi:10.2217/fmb-2020-0027

Genome Sequence-Based Curation of PubMLST Data Challenges Interspecies Recombination in the <i>Burkholderia</i> <i>Cepacia</i> Complex

2020· editorial· en· W3087597930 on OpenAlex

Why this work is in the frame

A frame that forgets how it found something cannot be audited. These are the routes that admitted this work.

aboutThe title or abstract carries a Canadian signal from the geographic lexicon.
no affNo Canadian affiliation: this work is invisible to an affiliation-only frame.
No Canadian affiliation. An affiliation-only frame, the usual design, would never have seen this work. It is one of the works that make the case for inverting the frame.

Bibliographic record

VenueFuture Microbiology · 2020
Typeeditorial
Languageen
FieldMedicine
TopicCystic Fibrosis Research Advances
Canadian institutionsnot available
FundersUniversity of OxfordWellcome Trust
KeywordsGenomeBiologyBurkholderia cepacia complexGeneticsSequence (biology)Whole genome sequencingComputational biologyBurkholderiaBacteriaGene

Abstract

fetched live from OpenAlex

Multilocus sequence typing (MLST) has been the gold standard for typing and identification of a wide range of bacteria for two decades [1][2][3].Public MLST databases allow researchers worldwide to analyze and deposit data, and enable the study of the global prevalence and epidemiology of a broad range of bacteria [3,4].A Burkholderia cepacia complex (Bcc) MLST scheme based on partial atpD, gltB, gyrB, recA, lepA, phaC and trpB gene sequence analysis was developed for both species and strain level differentiation [5][6][7].PCR primers were subsequently improved to reliably amplify the target loci from both Bcc and non-Bcc Burkholderia bacteria and to enable the use of a single primer set for amplification and sequencing [8].The large number of recent publications that used MLST and the accompanying Bcc PubMLST database as a tool for epidemiological studies shows that MLST is a well-established method that enabled outbreak surveillance, shed light on the global distribution of strains and elucidated Bcc epidemiology and population structure [9].While the first few hundred sequence types were primarily originating from European, American and Canadian isolates, there has been an increase in submissions from Australia and countries in Asia and South-America.Reproducibility and portability have been considered major advantages of MLST over earlier typing and identification methods [1,2].In today's genomics era, traditional Sanger sequencing of MLST loci is gradually replaced by the extraction of MLST alleles from next-generation sequencing data, thus sustaining the continued use of the same MLST schemes [2,10].As curators of the Bcc PubMLST database [3,11] we observed that genome sequence derived MLST data revealed several types of conflicts with earlier MLST data that were generated through Sanger sequencing.We generated genome sequences from high-coverage Illumina data for 113 Bcc isolates (method as previously described by Peeters et al. [12], [unpublished data]) for which Sanger sequencing based MLST data were available; for 34 of these isolates (30%) there was a conflict between the genome sequence derived and earlier MLST data.Generally, two types of conflict were found.In one type of conflict the genome sequence derived MLST alleles revealed one or a few single nucleotide polymorphisms compared with the earlier MLST data.An example of this type of error was found for Burkholderia multivorans outbreak strain C1576 [13], for which the initial MLST analysis yielded lepA-8 and trpB-6 [7], while more recent analyses uncovered lepA-224 [14] (1/397 nucleotide differences) and trpB-415 (GenBank/ENA accession number ERS784904) (3/301 nucleotide differences), changing the sequence type from ST-27 into ST-899.Because the coverage of Illumina data by far exceeds that of traditional Sanger sequencing, it is not unexpected to find a few false single nucleotide polymorphisms in the original MLST data [15,16].

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.001
metaresearch head score (Gemma)0.002
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesMeta-epidemiology (narrow)
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Not applicable · Consensus signal: Not applicable
GenreCandidate signal: Editorial · Consensus signal: Editorial
Teacher disagreement score0.347
Threshold uncertainty score1.000

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0010.002
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0010.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0010.000
Research integrity0.0010.001
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.090
GPT teacher head0.341
Teacher spread0.251 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it