Evidence map›Paper›PMID 35210470›Full record

ArticleScientific reports2022

Improving the efficiency and effectiveness of an industrial SARS-CoV-2 diagnostic facility.

Julie A Douthwaite, Christopher A Brown, John R Ferdinand, Rahul Sharma, Jane Elliott, Molly A Taylor, Nancy T Malintan, Hannah Duvoisin, Thomas Hill, Oona Delpuech and 40 more

Abstract read
In one paragraph

Article in Scientific reports, 2022. 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. 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

50 authors.

Julie A Douthwaite *BioPharmaceuticals R&D, AstraZeneca, Cambridge, UK. julie.douthwaite@astrazeneca.com.
Christopher A Brown *Charles River Laboratories, Chesterford Research Park, Saffron Walden, UK. christopher.brown@crl.com.
John R Ferdinand *Charles River Laboratories, Chesterford Research Park, Saffron Walden, UK.
Rahul Sharma *Charles River Laboratories, Chesterford Research Park, Saffron Walden, UK.
Jane ElliottBioPharmaceuticals R&D, AstraZeneca, Cambridge, UK.
Molly A TaylorBioPharmaceuticals R&D, AstraZeneca, Cambridge, UK.
Nancy T MalintanBioPharmaceuticals R&D, AstraZeneca, Cambridge, UK.
Hannah DuvoisinBioPharmaceuticals R&D, AstraZeneca, Cambridge, UK.
Thomas HillCharles River Laboratories, Chesterford Research Park, Saffron Walden, UK.
Oona DelpuechBioPharmaceuticals R&D, AstraZeneca, Cambridge, UK.
Alexandra L OrtonBioPharmaceuticals R&D, AstraZeneca, Cambridge, UK.
Haidee PittBioPharmaceuticals R&D, AstraZeneca, Cambridge, UK.
Fred KuenziCharles River Laboratories, Chesterford Research Park, Saffron Walden, UK.
Simon FishCharles River Laboratories, Chesterford Research Park, Saffron Walden, UK.
David J NichollsBioPharmaceuticals R&D, AstraZeneca, Cambridge, UK.
Anna CuthbertBioPharmaceuticals R&D, AstraZeneca, Cambridge, UK.
Ian RichardsCharles River Laboratories, Chesterford Research Park, Saffron Walden, UK.
Giles RatcliffeCharles River Laboratories, Chesterford Research Park, Saffron Walden, UK.
Abhishek UpadhyayBioPharmaceuticals R&D, AstraZeneca, Cambridge, UK.
Abigail MarklewCharles River Laboratories, Chesterford Research Park, Saffron Walden, UK.
Craig HewittBioPharmaceuticals R&D, AstraZeneca, Cambridge, UK.
Douglas Ross-ThrieplandBioPharmaceuticals R&D, AstraZeneca, Cambridge, UK.
Christopher BrankinBioPharmaceuticals R&D, AstraZeneca, Cambridge, UK.
Matthieu ChodorgeBioPharmaceuticals R&D, AstraZeneca, Cambridge, UK.
Gareth BrowneBioPharmaceuticals R&D, AstraZeneca, Cambridge, UK.
Palwinder K ManderGSK R&D, Stevenage, UK.
Ruud M DeWildtGSK R&D, Stevenage, UK.
Shane WeaverGSK R&D Tech, Stevenage, UK.
Penny A SmeeGSK R&D Tech, Stevenage, UK.
Joost van KempenGSK R&D, Stevenage, UK.
Jon G BartlettGSK R&D, Stevenage, UK.
Paula M AllenGSK R&D, Stevenage, UK.
Emma L KoppeGSK R&D, Stevenage, UK.
Charlotte A AshbyGSK R&D, Stevenage, UK.
Julian D PhippsGSK R&D, Stevenage, UK.
Nalini MehtaGSK R&D, Stevenage, UK.
David J BrierleyGSK R&D, Stevenage, UK.
David G TewGSK R&D, Stevenage, UK.
Melanie V LeveridgeGSK R&D, Stevenage, UK.
Stuart M BaddeleyGSK R&D, Stevenage, UK.
Ian G GoodfellowDivision of Virology, Department of Pathology, University of Cambridge, Cambridge, UK.
Clive GreenBioPharmaceuticals R&D, AstraZeneca, Cambridge, UK.
Chris AbellVice Chancellor's Office, University of Cambridge, Cambridge, UK.
Andy NeelyVice Chancellor's Office, University of Cambridge, Cambridge, UK.
Ian WaddellCharles River Laboratories, Chesterford Research Park, Saffron Walden, UK.
Steve ReesBioPharmaceuticals R&D, AstraZeneca, Cambridge, UK.
Patrick H MaxwellSchool of Clinical Medicine, University of Cambridge, Cambridge, UK.
Menelas N PangalosBioPharmaceuticals R&D, AstraZeneca, Cambridge, UK.
Rob HowesBioPharmaceuticals R&D, AstraZeneca, Cambridge, UK.
Roger ClarkCharles River Laboratories, Chesterford Research Park, Saffron Walden, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

On 11th March 2020, the UK government announced plans for the scaling of COVID-19 testing, and on 27th March 2020 it was announced that a new alliance of private sector and academic collaborative laboratories were being created to generate the testing capacity required. The Cambridge COVID-19 Testing Centre (CCTC) was established during April 2020 through collaboration between AstraZeneca, GlaxoSmithKline, and the University of Cambridge, with Charles River Laboratories joining the collaboration at the end of July 2020. The CCTC lab operation focussed on the optimised use of automation, introduction of novel technologies and process modelling to enable a testing capacity of 22,000 tests per day. Here we describe the optimisation of the laboratory process through the continued exploitation of internal performance metrics, while introducing new technologies including the Heat Inactivation of clinical samples upon receipt into the laboratory and a Direct to PCR protocol that removed the requirement for the RNA extraction step. We anticipate that these methods will have value in driving continued efficiency and effectiveness within all large scale viral diagnostic testing laboratories.

Indexed as

COVID-19COVID-19 TestingSARS-CoV-2HumansLaboratoriesUnited Kingdom

Identifiers

PMID35210470
PMCPMC8873195

What OpenQuestion holds

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Registered trials

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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.