Evidence map›Paper›PMID 30102688›Full record

ArticlePLoS biology2018

Provenance and risk in transfer of biological materials.

Jane Nielsen, Tania Bubela, Don R C Chalmers, Amber Johns, Linda Kahl, Joanne Kamens, Charles Lawson, John Liddicoat, Rebekah McWhirter, Ann Monotti and 3 more

Abstract read
In one paragraph

Article in PLoS biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Opportunities for promoting open data in the Caribbean through biobanks.Revista panamericana de salud publica = Pan American journal of public health · 2025
    Article
  3. Review
  4. Article
  5. 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

13 authors.

Jane NielsenCentre for Law and Genetics, Faculty of Law, University of Tasmania, Hobart, Tasmania, Australia.ORCID 0000-0002-3005-0047
Tania BubelaFaculty of Health Sciences, Simon Fraser University, Burnaby, Canada.
Don R C ChalmersCentre for Law and Genetics, Faculty of Law, University of Tasmania, Hobart, Tasmania, Australia.
Amber JohnsCancer Division, Garvan Institute of Medical Research, Darlinghurst, New South Wales, Australia.
Linda KahlBioBricks Foundation, San Francisco, California, United States of America.
Joanne KamensAddgene, Cambridge, Massachusetts, United States of America.
Charles LawsonGriffith Law School and Australian Centre for Intellectual Property in Agriculture, Griffith University, Gold Coast, Queensland, Australia.
John LiddicoatFaculty of Law, University of Cambridge, Cambridge, United Kingdom.
Rebekah McWhirterCentre for Law and Genetics, Faculty of Law, University of Tasmania, Hobart, Tasmania, Australia.
Ann MonottiFaculty of Law, Monash University, Clayton, Victoria, Australia.
James ScheibnerCentre for Law and Genetics, Faculty of Law, University of Tasmania, Hobart, Tasmania, Australia.
Tess WhittonCentre for Law and Genetics, Faculty of Law, University of Tasmania, Hobart, Tasmania, Australia.
Dianne NicolCentre for Law and Genetics, Faculty of Law, University of Tasmania, Hobart, Tasmania, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Whereas biological materials were once transferred freely, there has been a marked shift in the formalisation of exchanges involving these materials, primarily through the use of Material Transfer Agreements (MTAs). This paper considers how risk aversion dominates MTA negotiations and the impact it may have on scientific progress. Risk aversion is often based on unwarranted fears of incurring liability through the use of a material or loss of control or missing out on commercialisation opportunities. Evidence to date has suggested that complexity tends to permeate even straightforward transactions despite extensive efforts to implement simple, standard MTAs. We argue that in most cases, MTAs need do little more than establish provenance, and any attempt to extend MTAs beyond this simple function constitutes stifling behaviour. Drawing on available examples of favourable practice, we point to a number of strategies that may usefully be employed to reduce risk-averse tendencies, including the promotion of simplicity, education of those engaged in the MTA process, and achieving a cultural shift in the way in which technology transfer office (TTO) success is measured in institutions employing MTAs.

Indexed as

HumansLaboratory ChemicalsLiability, LegalOwnershipResearchRiskLaboratory Chemicals

Identifiers

PMID30102688
PMCPMC6107254

What OpenQuestion 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 OpenQuestion graph.