A COVID perspective: TL;DR - the pandemic in the developed world has shifted due to successful vaccines, though plenty of complex and tricky scenarios to navigate; the developed world is in the midst of even harsher transmission rate from Delta.
Context: I am an expert in human genetics and bioinformatics. I know experts in viral genomics, infectious epidemiology, public health, clinical trials and immunology. I have some COIs: I am longstanding consultant to Oxford Nanopore (sequencing company) and am on the Ox/AZ trial
With the perspective of a glorious holiday in Northumberland, the last week disconnected from work and twitter, I have some bigger picture musings on the pandemic from my perspective.
The first is just how good the vaccines are - and thus how lucky we are - we have at least 4 really good vaccines in that they radically change the likelihood of severe disease from SARS-CoV-2 infection and clearly at least blunt transmission.
This was not a given; the vaccines could have plain not worked (some vaccines candidates for SARS-CoV-2 didn't). There could have been unacceptable adverse effects (adverse effects are present but very rare). They could have only moderately ameliorated severe disease.
As such the rather straightforward strategy of vaccinating as closely to everyone at risk of severe disease (crudely >50) and as large a proportion of the rest population as one can reach is sound; Europe (UK included) and Israel are showing the way here and it... looks sound.
(I note that the vaccines also seem to reduce the incidence of LongCOVID, which makes sense, and so there is an extra benefit for vaccinating people not at risk beyond suppressing transmission as clearly LongCOVID exists and is not nice)
However, UK and Israel are also showing the outline of the new normal; SARS-CoV-2 still in circulation, and the Delta variant infecting a number of double vaxxed people - far far less likely to lead to severe disease, but still transmitting. This looks like to me the new normal.
This is ... in line with the other 4 circulating human coronaviruses, where there is differential (and waning) immunity coupled with antigenic drift of the viruses (the viruses tweaking their key "display" regions) is the endemic, long term situation for these infectious agents
And so we will likely have a 5th coronavirus, SARS-CoV-2 giving many people "the common cold" which causes sometimes "viral pneumonia" and "viral triggered auto-immunity"; I suspect SARS-CoV-2 will be the nastiest of the 5 for a long time.
Hence the discussion and plans around vaccine boosters for the most at risk, and the new normal is going to have darker clouds from coronavirus infection for a while.
(Note: elimination of SARS-CoV-2 is gone from "very unlikely" to "very very unlikely, impossible in the mid term" in my view - just the numbers of humans, the infectivity, and also now documented animal reservoirs means this is not a credible short or mid term strategy)
Getting to this new normal means that very nearly everyone on the planet must either be vaccinated or infected. And the supply and distribution of vaccines is going to be the main reason for which route people take, though anti-vax/vaccine hesitancy sentiment is next.
I am *not* an expert (nor know well experts) on vaccine production and then distribution - the main thing I know is it is very complex both in actually doing it and regulation, but this is where the drama is worldwide. All wind to the sails of the production sites.
The impact on the developing world of lower vaccine supply is going to be ... harsh. Watching the Delta wave propagate through the largely unvaccinated India, and the impact of people and healthcare delivery is awful.
This means improving vaccine production and its supply globally is the single most important thing that can happen over the next months.
In developed countries with vaccine supply, there seems to be two phases: vaccinating the vast majority of high risk individuals and a large proportion of others, and then titrating infection across this population at a sensible rate.
The Delta variant has enough infectivity/transmission in a largely vaccinated society for there to be another wave "on top" - Israel having achieved something like community immunity with Alpha is now navigating this Delta-on-vaccination wave.
Other countries are approaching this from the other side of increasing vaccination and titrating out NPIs - the country I know best here is the UK, and it seems this strategy looks sensible but with an angst filled last titration step of release with poor messaging and tactics
Most of Western Europe will be in broadly the same place as Israel and UK sometime over this summer (or already there); France's somewhat lower vaccine uptake makes their navigation of the summer probably the most complex in Western Europe.
However, there are other countries in Europe which really need to accelerate their vaccine delivery before the faster transmitting Delta wave crashes over them. The growth in infection in UK and Netherlands just shows how much faster Delta is vs Alpha or the earlier variants.
Australia + New Zealand - which had an excellent elimination + quarantine scheme at start of the pandemic now need to transition to this high vaccination strategy - the elimination + quarantine is harder to hold vs Delta (as seen in Sydney now) and is not a mid term strategy
Here vaccine hesitancy (spiced with the weird anti-vax conspiracy theories) needs to be overcome, ideally without having to have serious transmission and healthcare impact to "make it real".
But the developed world country I worry about the most is the US. By the numbers the US vaccination level is reasonable if slowing; but the aggregate numbers I think hides a stronger regional variation, and in particular a larger number of at risk people not vaccinated.
Other people will know the numbers and drivers better than me, but from afar this is both the complexity of reaching marginalised communities in the US + also the alignment of anti-vax sentiment to partisan politics. The latter gets the press; the former is probably as important.
Again, one might expect that the reality of people going into hospital at high rate will be the backstop to get over vaccine hesitancy, but I worry about just the speed and momentum of infection compared to how fast one can turn around vaccination rates.
I think therefore the US is going to have a tough summer - in particular in the South and Midwest - and the frustrating is that this is all so avoidable.
But the developed world problems - even this - are small in the context of the global problem of vaccine supply. Plenty of complex production issues at the heart of this; then logistics and with politics stirred in across this.
We are definitely not out of the pandemic yet.

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More from @ewanbirney

5 Aug
Had another moment of "well, yes, but people *are* different" and "you geneticists use continental groups in your analysis" as we skirted around discussions of ethnicity / race in health impacts. TL;DR Partially correct but the underlying mindset that ethnicity=genetics is wrong
Let's deal with the correct things first. Yes, people are different partly (sometimes mainly) due to genetics. Visibly, eg height, weight, hair colour, skin colour, smoking habits + invisibly, eg cholesterol levels, heart trabeculation levels, likelihood of getting breast cancer
Some of these visible differences we integrate into the gestalt assessment of ourselves and others for ethnicity, as represented by self identified ethnicity boxes which people tick, eg "Black British, White English, British Indian, British xxx", gloriously variable by society
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4 Aug
Ah. I love the smell of freshly baked data/analysis, well controlled false discovery rate (QQ plot) and just ... so many results. Which of the thousands of beautiful stars in the sky does one pull out to discuss? Biology is so endless and wonderful in its detail...
... to alter (butcher?) a passage from a far far wiser and more thoughtful man than me....
It is interesting to contemplate a tangled set of genetic results, associated to both well known genes and entirely anonymous regions of the genome, stories from physiology of old and hints of new insights, and to reflect ...
Read 5 tweets
4 Aug
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There is, for me, a similar history of technology / medicine about the complex introduction of Xrays into medicine (I blogged about this 6 years - (! 6 years!) ago - ewanbirney.com/2015/10/genomi…
The journey of Xrays from spanking new whizzy technology to routine part of medicine is surprisingly complex - it involves twists and turns, inappropriate use of technology "just for fun" (echos of 23andme), and non obvious advocates for the uptake of the technology.
Read 4 tweets
22 Jul
A personal view point on the #AlphaFold announcement today from the @DeepMind and @emblebi team, part of @embl. TL;DR - I am *still* pinching myself about this.
When @demishassabis and the AlphaFold team first presented the results from CASP to me last November I genuinely almost fell off my chair. I think I swore quite a bit (in a British way) in amazement.
One of the reasons was I knew how rigorous CASP was - 20 years ago people published all sorts of "solving the folding problem" which then... didn't work beyond the training set. CASP cleverly used the fact that there are genuinely unknown structures each year solved by experiment
Read 15 tweets
28 Jun
*trumpets* A new preprint by colleagues in @PHE_uk from @isaperena's group and myself (my first infectious epidemiology paper!) on single source transmission of COVID19 using viral genotyping to understand relative risk of transmission settings. papers.ssrn.com/sol3/papers.cf…
Background; we have known for a long time that there is overdispersion of SARS-CoV-2 transmission; some estimates are that 20% of settings/events account for 80% of transmission. Understanding where these transmission events occur is important for non-pharmaceutical interventions
Furthermore, if we can be confident of spotting these individual small-scale super-spreading events and inform other individuals who are at risk of infection at the same time we can highlight people who are at the higher risk for infection, eg, asking them to get a test.
Read 23 tweets
21 Jun
A group of us (@minouye271, @JenniferRaff, @aylwyn_scally @AdamRutherford and myself) have written a piece on the language we use in genetics; untangling from previous sometimes racist language and being more precise and less harmful. We welcome feedback. arxiv.org/abs/2106.10041
There are some straightforward 'stop using this term' aspects (the use of "Caucasian" for example); there are some complex "what does this term mean" (ethnicity labels, the ethnicity/race duality in US vs just ethnicity in UK / Europe) and then technical stuff on GWAS >>
The technical piece is about how we describe the common place GWAS protocol of subselecting a group people in cohorts for association analysis; a reminder that the standard process has two steps to achieve pseudo-randomisation of non-genetic factors to genetic factors
Read 14 tweets

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