Authors retract meningitis paper over permission — but data are in a public database

plos1A study characterizing subtypes of the bacteria that cause bacterial meningitis is being retracted after the authors didn’t have permission to publish the data, even though the data itself remain available in a public database.

The paper, in PLOS ONE, relied on a laboratory collection of patient samples. In October, the authors retracted it because they “did not have permission” from the laboratory “to publish the data in their current form.” The data — anonymized — are now available at PubMLST.

Here’s the retraction notice, published on October 16: Continue reading Authors retract meningitis paper over permission — but data are in a public database

Cancer researcher cleared of misconduct, inquiry finds “genuine error or honest oversight”

Khachigian
Levon Khachigian

An investigation at the University of New South Wales in Australia has determined that a long-accused cancer researcher did not commit misconduct.

The investigation did find instances when Levon Khachigian breached the code of conduct, but Continue reading Cancer researcher cleared of misconduct, inquiry finds “genuine error or honest oversight”

Do science findings feel more novel, robust? They are — at least, in language

BMJ-Avatar-160x160

Do you think the write-up of scientific results has gotten more rosy over time? If so, you’re right — the use of positive language in science abstracts has increased by 880% since 1974, according to new findings reported in the British Medical Journal.

Researchers led by Christiaan H Vinkers at the University Medical Center Utrecht in The Netherlands found that, among PubMed abstracts: Continue reading Do science findings feel more novel, robust? They are — at least, in language

Having non-replicable data may not hurt your rep, says study

plosoneAlthough many scientists fear putting their data to the test of replication efforts, due to the embarrassment they’d feel if their findings couldn’t be repeated, a new study suggests those fears are unfounded.

The paper, published last week in PLOS ONE, found that scientists overestimate how much having non-replicable data will hurt their careers, and the community values those who are honest about what went wrong.

Specifically, as the authors note:

Continue reading Having non-replicable data may not hurt your rep, says study

We’re wasting a lot of research funding using the wrong cell lines. Here’s one thing we can do.

If you could help reduce the waste of tens of billions of dollars per year in research spending, you’d do it, right?

This is the second in a series of two guest posts about the havoc misidentified cell lines can wreak on research, from Leonard P. Freedman, president of the Global Biological Standards Institute. Freedman who published a paper last summer detailing the financial costs of non-reproducible research — namely, tens of billions of dollars per year. Some of that non-reproducible research is due to the use of contaminated or misidentified cell lines. He writes about one key step to tackling the problem: Ask every scientist to use a relatively inexpensive technique to validate the identity of their cell lines.

Meanwhile, we have to deal with the issue of all the previously published papers that relied on problematic cell lines, now contaminating the scientific literature. Scroll down to the bottom of the post to take a poll on what you think should be done about those papers.

Leonard Freedman
Leonard Freedman

As new frontiers of science emerge, from Pluto to proteins, the very cornerstone of the scientific process—reproducibility—has also reared its head as a huge problem. Estimates of irreproducibility rates of published peer-reviewed papers range from 51% to 89%. An analysis that two colleagues and I recently published in PLOS Biology suggests the U.S. spends $28 billion per year on non-reproducible preclinical research; global spending could be up to $60 billion per year. This lack of reproducibility typically results from cumulative errors or flaws in one or more of the following areas: biological reagents and reference materials, study design, laboratory protocols, and data analysis and reporting. Given the size, scale, and especially the complexity of reproducing preclinical research, there is no single magic bullet fix. This is a difficult issue for scientists to own up to, and for the public to grasp.

However, an approach that has demonstrably addressed similar challenges in other complex and evolving industries, such as those involved in the founding of the Internet, is the expanded use of community-based voluntary standards and best practices. And here’s where we start: Continue reading We’re wasting a lot of research funding using the wrong cell lines. Here’s one thing we can do.

Hundreds of researchers are using the wrong cells. That’s a major problem.

Amanda Capes-Davis
Amanda Capes-Davis

What if we told you that approximately 1 in 6 researchers working with human cells are using the wrong cell line? In other words, they believe they are studying the effects of a drug on breast cancer cells, for instance, but what they really have are cells from the bladder. That is the unfortunate reality in life science research today, affecting hundreds of labs. It’s a major source of problematic papers which cannot be replicated, wasting scientists’ time and funding.

We’re pleased to present a guest post from Amanda Capes-Davis, chair of the International Cell Line Authentication Committee (ICLAC), a voluntary scientific committee created to improve awareness of misidentified cell lines. She also collects news about cell line and culture contamination. This is the first in a series of two posts from guest authors about how problematic cell lines are contaminating the scientific literature, and how we can clean it up.  

In 2010, I worked alongside Ian Freshney of Glasgow University and other colleagues to publish a list of cross-contaminated or otherwise misidentified cell lines in the International Journal of Cancer. This database of false cell lines is now curated by the International Cell Line Authentication Committee (ICLAC).

All of us who have contributed to the database are aware that cross-contamination is an important ongoing problem.  But I think the number of cell lines affected was a surprise, even to many of us in the field who see these problems on a daily basis. Continue reading Hundreds of researchers are using the wrong cells. That’s a major problem.

My life as a whistleblower: Q&A with Peter Wilmshurst

We’re presenting a Q&A session with Peter Wilmshurst, now a part-time consultant cardiologist who has spent decades embroiled in misconduct investigations as a whistleblower.

Dr-Peter-Wilmshurst-007
Peter Wilmshurst

Retraction Watch: A UK judge recently upheld two findings of dishonesty by the Medical Practitioners Tribunal Service against Andrew Dowson, director of headache services at King’s College Hospital and your former co-investigator. Were you pleased with the verdict? (Last week, Dowson also began a four-month suspension from practicing medicine in the UK.) 

Peter Wilmshurst: In part, because I was pleased that he was shown to be dishonest, because I knew that he was, which was why I reported him. But I wasn’t pleased in the sense that I don’t think the investigation dealt with all the issues involved in the Migraine Intervention with STARflex Technology (MIST) Trial.

RW: What additional issues did you hope to see addressed? Continue reading My life as a whistleblower: Q&A with Peter Wilmshurst

Did a clinical trial proceed as planned? New project finds out

Ben Goldacre
Ben Goldacre

A new project does the relatively straightforward task of comparing reported outcomes from clinical trials to what the researchers said they planned to measure before the trial began. And what they’ve found is a bit sad, albeit not entirely surprising.

As part of The Compare Project, author and medical doctor Ben Goldacre and his team have so far evaluated 36 clinical trials published by the top five medical journals (New England Journal of Medicine, the Journal of the American Medical Association, The Lancet, Annals of Internal Medicine, and British Medical Journal). Many of those trials included “switched outcomes,” meaning the authors didn’t report something they said they would, or included additional outcomes in the published paper, with no explanation for the change.

Here are the latest results from the project, according to its website:

Continue reading Did a clinical trial proceed as planned? New project finds out

ORI names new director, Colorado’s Kathy Partin

Kathy Partin
Kathy Partin

The director of the Research Integrity & Compliance Review Office at Colorado State University (CSU) is the new head of the U.S. Office of Research Integrity, taking over a position that has been vacant for more than a year and a half.

A spokeswoman for the Department of Health and Human Services confirmed for us the new appointment, which was first reported by The Report On Research Compliance today. Continue reading ORI names new director, Colorado’s Kathy Partin

A Retraction Watch retraction: Our 2013 advice on reporting misconduct turns out to have been wrong

2015_06_miniNearly three years ago, our co-founders Ivan Oransky and Adam Marcus penned a column in Lab Times suggesting ways for readers to report alleged scientific misconduct. They are now retracting that advice.

In the retracted column, they suggested initially contacting the editor of the journal that published the potentially problematic work, and if the editor suggests it, contact the authors of that work. In their latest column for Lab Times, Oransky and Marcus say: Forget that advice.  Continue reading A Retraction Watch retraction: Our 2013 advice on reporting misconduct turns out to have been wrong