Open peer review failed

It was an interesting experiment that started on June, 1 in the Nature office: a first trial of of open peer review. Of the 10,000 papers received every year, 6,000 are immediately rejected and eventually 700 published after peer review. The result of the trial, however, is disappointing:

We sent out a total of 1,369 papers for review during the trial period. The authors of 71 (or 5%) of these agreed to their papers being displayed for open comment. Of the displayed papers, 33 received no comments, while 38 (54%) received a total of 92 technical comments.

The trial provoked some web traffic with approx. 800 page views/day. Welcome back to the altruism thread, the discussion may be followed at their blog, yea, yea.


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Innate immunity is species-, individual, organ-specific

In a previous paper I have questioned if LPS

nanogram exposure on the pulmonary epithelium will supersede the gram-wise exposure on the gut mucosa.

This may indeed work as now shown by Eyal Raz in a commentary in Nature Immunology where previous TLR studies

typically reproduce the splenic version of innate immunity (the spleen is used here as a metaphor for the sterile internal environment).

In the lung only the alveolar space is thought to be sterile while macrophages should not be in a constant state of activation (as inflammation would compromise gas exchange).

There are now several indicators for a lung-specific regulation of innate immunity: TLR9 is expressed in human plasmacytoid dendritic cells while TLR4 is only on myeloid DCs; TGFB-ß mediated crosstalk between alveolar macrophages and epithelial cells seems to be unique in the lung; in addition indeolamine induction or surfactant production is not found elsewhere. Yea, yea.


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He can run slowly

if you want to see Crison and me in the same stadium, you must bid him slacken his speed to mine, for I cannot run quickly, and he can run slowly.

(from Platons Protagoras dialogue English|German).

firstmonday has a wonderful paper “More, Faster, Better: Governance in an Age of Overload, Busyness, and Speed” basically arguing that the vast sources of information has a rather paradoxical effect: the abundance of information rather disconnects and distances us from ourselves and the world around us.

Immersed in a sea of media, information sources, technologies and devices, many of us are now becoming aware of the downside — some would say the dark side — of these powerful new modes of communicating and acting.

The mere number of papers being published even in my most genuine area of interest is impossible to monitor at the end of 2006 – bioscience looses more and more scientia. Although papers still have a “discussion” section, there is no more discussion as references are getting more and more eclectic.

The Levy paper in firstmonday is a “must read” – in particular the chapter on

Vannevar Bush, an American born in 1890, was trained as an electrical engineer and for the first part of his career worked as a professor and an administrator at MIT…. Bush was famous enough to appear on the cover of Time in April of 1944. Yet today he is best remembered not for his technical work or his contribution to winning the war, but for an article he published in the Atlantic Monthly in July, 1945, titled “As We May Think”

and what he says about two kinds of thought: routine or repetitive or logical thinking along an accepted groove – literature scan, arithmetic operations all that technical stuff that can be automated: In contrast there is mature, creative thought, deep, original thinking, reasoning – without any mechanical substitute. Levy makes the point that

Certainly the easy availability of information and the increasing pace of life can at times be empowering and even exhilarating, but too much stimulation can lead to numbing, a loss of focus, and withdrawal: it can dumb down, enervate and even stupefy.

the information overload (with less reliable, often questionable) information leads to a deprivation of mature thinking that severely affects now the academic world

Yet today’s universities — their faculty, students, and staff — are increasingly caught up in the current cultural frenzy; academics are now busier and more overloaded than ever before. The pressure on faculty to obtain outside funding is intense and increasing as the pool of available funds shrinks; time spent searching for potential funding sources, writing grant proposals, and shepherding them through intricate bureaucratic procedures is simply added on to the other expectations of the job…. increased student expectations that instructors should and will be available for consultation at all hours of the day and night, weekends included. E–mail has also made professors that much more reachable by the general public, the press, and academics at other institutions…

What can be done? Prescreening of relevant science by (institutionalised) editors or (anarchic) blogs? And by which criteria?


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Quod licet Jovi not licet Bovi

Rolf Zinkernagel in a commentary in Nature Immunology explains that today almost everything can be measured – and a nearly uncontrollable complexity often paired with weak detection methods renders experiments almost unrepeatable. His recommendations are

Most if not all experiments have limitations. Therefore researchers must think and argue and do experiments contrary to published results and against biases.

Nearly all studies need some funding; funding is controlled by peer review; peer review usually prohibits these experiments. Yea, yea.


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Proteomics 73 years ago

Otto Warburg was not only lucky to win a Nobel prize but also three of his scholars. On of these, Hugo Theorell, describes the discovery of nicotinic acid amide as picrolonate in December 1933. The initial yield of the substance was poor – crystals of a few miligrams were obtained from 200 l of horse blood. Warburg estimated that they would have to kill all horses in Germany to find out the constitution. Theorell continues (quoted from Krebs: Warburg. 1981, p32)

Fortunately, they had the elementary analysis, melting point and the molecular weight. Now a friend of Warburg’s, Walter Schöller, who was the head of the Schering Kahlbaum Company Laboratory, made the simplest trick in the world: he looked into ‘Beilstein’ for substances with the same composition and melting point and within no time he said: “Well, this is nicotinic acid amide, synthesized by Mr so-and-so in 1878 or something like that.” Warburg’s comment was as laconic as usual: “Yesterday we could not buy it for any money in the world, today we can buy it for two marks a pound.”

Nicotinamide had powerful inhibitory effects on mycobacteria and led to the synthesis by Hoffman-La Roche of isonicotinic acid hydrazide or isoniazid – and Warburg had the chance to read his own obituary in The Times (Krebs, p.67) where he complained that the discovery of nicotinamide had been deliberately omitted (his former institute is here).
Looks pretty much that this discovery worked along the same strategy as proteomics today: 2-DE to tandem MS (MS/MS) and database lookup. Yea, yea.


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What would you choose?

At the moment I am reading the biography of Otto Warburg eloquently written by Hans Krebs. Here is a nice story about the banking house M. M. Warburg in Hamburg: Aby Warburg renounced his right to share in the banking business on the condition that his brothers would pay the bills for all the books that he deemed necessary for his library. The brothers enormously underrated the magnitude of this financial obligation – Aby Warburg (1866-1929) assembled a unique art history library which is now at London University. Would you like to have a brother who is a banker or would you like to be a banker with such a brother?


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BMJ Christmas edition

We are already waiting for the BMJ. This year

  • Physicians in opera: Stefan Willich about Le Nozze di Figaro
  • Sword swallowing and its side effects: Brian Witcombe’ s finding that sword swallowers run a higher risk of injury
  • Daisy the Doctor, Dr Dose, Dr Grizzly, Dr Amelia Bedelia, and colleagues: Monica Lalanda works on the image of doctors in children books: kind, professional, and reassuring
  • Phenotypic differences between male physicians, surgeons, and film stars – comparative study: Antoni Trillas rating of “good looking” men – the winner, sorry, are not the surgeons
  • From a 16th century monastery to a 21st century orthopaedic hospital: P (not Alberto) Tomba, worth a visit
  • and much more

Yea, yea.


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Philosophy, the voice of rationality in the dialogue with biological sciences (podcast)

Last week I attended a meeting in Neuherberg about the future of science and ethics in medicine and biology. Prof. Jürgen Mittelstraß (Konstanz) gave the introductory lecture, Prof. Herwig Hulpke, Prof. Friedrich Wilhelm Graf and Prof. Klaus Peter participated in the discussion moderated by Fraua Ferlemann (BR). The lecture by Prof. Mittelstraß was remarkable, I am offering here a 60 MINUTE PODCAST [in German only] while the manuscript will follow later in January 2007. Please let me know if you want the full audio records of the 2 hour meeting.

Prof. Mittelstraß (left) and Prof. Graf (right) during the discussion
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A revival of DNA pooling

My interest in DNA pooling was always strong; we have developed methods doing this on the mass spec platform and applied it to the HLA region. I had, however, doubts if testing pools by less accurate methods like chip hybridization will work. The January issue of the AJHG now has a fascinating article how pooling may even work on the Affymetrix platform. Yea, yea.

Addendum

DNA pooling can be even used in family context, see Wen Chung Lee in Cancer Epidemiology 2005 or Neil Risch in Genome Research 1998.


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Genetic tango

Science daily reports an interesting study how a protein recognizes a particular DNA binding site

Structural changes in both the protein and DNA, sometimes with the DNA within the complex kinked or sharply bent, allow for the specific contacts needed for a tight DNA-protein fit. Scientists think DNA is largely passive in this genetic tango. But new findings by Anjum Ansari, associate professor of biophysics at the University of Illinois at Chicago, suggest DNA may not be the wallflower that many had assumed…

Yea, yea.


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454 or 0815 or 4911

In a recent book chapter we discussed new genotyping and sequencing technologies. Our concluding remarks haven´t changed so much – it seems that realtime detection of single molecules is still not possible; micro electropheresis based methods have already reached their limit while sequencing by hybridization has severe restrictions when it comes to de novo (or re-) sequencing of whole genomes. At least for research purpose I expect that whole genome re-sequencing will replace current SNP based disease mapping. So far, sequencing by synthesis seems to be one of the few HT methods that already works at that scale. The 454 platform consists of 3 consecutive steps:

  1. DNA library preparation starts with genomic DNA (after fragmentation and adaptor ligation the single-stranded template DNA libraries are isolated and assessed (takes ~4 hours)
  2. sstDNA is emulsificated, then amplified and recovered on beads before sequencing primer are being annealed (takes 1 day)
  3. After washing, so called PicoTiterPlates are prepared and a process started that looks like a combination of pyrosequencing reaction, correct me if I am wrong, a pyrophospate dependent enzyme cascade emitting light being recorded by a CCD camera that watches each of the ~200,000 holes (takes ~6 hours according to a recent paper in GenomXPress 2/06, figures at 454.com)

With an average read length of 100 bp and 200,000 fragments (resulting in 20 Mb) in 6 hours, the throughput is about 60fold compared to Sanger sequencing. The recent Neanderthal paper raises five arguments why the 454 sequencing platform is extremely well suited for analyses of bulk DNA extracted from ancient remains.

  1. … it circumvents bacterial cloning, in which the vast majority of initial template molecules are lost during transformation and establishment of clones.
  2. … because each molecule is amplified in isolation from other molecules it also precludes template competition, which frequently occurs when large numbers of different DNA fragments are amplified together.
  3. … its current read length of 100–200 nucleotides covers the average length of the DNA preserved in most fossils.
  4. … it generates hundreds of thousands of reads per run, which is crucial because the majority of the DNA recovered from fossils is generally not derived from the fossil species, but rather from organisms that have colonized the organism after its death.
  5. … because each sequenced product stems from just one original single-stranded template molecule of known orientation, the DNA strand from which the sequence is derived is known. This provides an advantage over traditional PCR from double-stranded templates, in which the template strand is not known, because the frequency of different nucleotide misincorporations can be deduced … damage that affects different bases differently.

Except of the low read length most of these observations would benefit large scale resequencing projects in human individuals. My main point for starting ASAP resequencing projects: So far we have not achieved a dense resolution of the genome while deep resequencing project (for example at the CRP locus) got astonishing results. We do not even know what is going on in the “noncoding” regions. Finally deletions and CNVs have been largely neglected – another look at this question in the EJHG.
The question remains, what does 454 mean – my inquiry is still pending. As far as I know 0815 was a machine gun in World War I and is a synomym for something repeatedly boring while 4911 is a street number and stands for a perfume. Yea, yea.


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Human breeding

There have been always attempts to make humans better – an idea that attracted people nearly every century. Ovid created Galatea from a statue, Goethe’s homunculus originated from a test tube, Mary Shelly created her monster from corpses, Bulgakows proletarian derived from a dog and Sloterdijks Menschenzüchtung by a fancy idea. There is only a minor difference at the end of 2006 – technical possibilities of genetic testing and genetic engineering are much higher developed. Yea, yea.


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Early biology blog

Sydney Brenner has written for many years a column in Current Biology called Loose Ends (Nature called him a man who talks a lot which is certainly unfair or at least not empirically proven – we are talking between 20,000 and 40,000 words every day). Loose ends seem to have influenced a whole generation of biologists – kitsch biology included. Yea, yea.


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Another layer of complexity in gene regulation

Yesterday evening I attended an excellent presentation by Nikolaus Rajewksy about microRNAs, small noncoding RNAs that are thought to have a role in posttranscriptional regulation. Nikolaus just moved 3 months ago from New York to follow Jens Reich at MDC in Berlin). Basically, he talked about his recent “l(ou)sy” paper and the “SNP” paper after giving a rather detailed history about the development of the field. It started in 1950 with Jacob and Monod, 1960 Britten and Davidson, 1970 Haywood (who even quit science after being dissappointed), finally to 1990 when the Ambros and Ruvkun labs discovered nematode microRNAs. Current research is mainly done in the Tuschl, Batel, Cohen, Lander and Rajewsky labs who produce the bulk of the 800 papers or so published in 2006.
Approximately 30% of genes are influenced by microRNAs, the total number of microRNA sites is under heavy debate (~22,000) as well as the number of human microRNAs (328); each microRNA regulates ~200 genes. Unfortunately there is still no highthroughput technique to detect targets. There is also no good prediction by free energy and even mismatches in the 5 prime of mRNA are possible (individual predictions can be obtained at Pictar that uses a hidden Markov model).
If I understood that correctly, miRNA are the feedback mechanism on RNA level (with transcription factors at the DNA level). He mentioned 3 classes known so far in humans: oncomiRNA, miRNA 375 myotrophin, and miRNA 122 acting on cholesterol (quite interesting as being described recently in the NEJM. The experimental knockdown of liver specific mouse microRNA shows ~300 up- and ~300 down regulated genes. Upregulated genes have in approximately 50% of cases one miRNA nucleus, downregulated ones have even less than average binding sites. There is no overrepresented GO category in upregulated genes but cholesterol is highly significant in downregulated genes whatever that means. Action of miRNA seem to heavily context dependent giving us many more questions than answers. Yea, yea.


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Epidemiology in wartime

What was the best paper in 2006? I am voting for a Lancet paper by Gilbert Burnham, Riyadh Lafta, Shannon Doocy and Les Roberts. Between May and July, 2006, they did a national cross-sectional cluster sample survey of mortality in Iraq. Data from 1849 households was gathered, 1474 births and 629 deaths were reported. As of July, 2006, there have been 654 965 excess Iraqi deaths occured as a consequence of the war.
If you can’t imagine what it means to work in war regions you may read the biography of Robert Capa (1913 –1954) who worked as a photographer in the many wars, and died in the First Indochina War. He did wonderful photos together with his girl-friend Gerda Taro, one of the first woman photographers who died by a tank accident already in the Spanish civil war at the age of 26. I will pay for the flowers if you visit her grave at Père Lachaise in Paris.

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Addendum

As expected, the study raised criticism: scienceblog:doi:10.1126/science.316.5823.355a


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