[HELICONIUS] FWD: Working group on genomics of repeated adaptation
James Mallet
jmallet at oeb.harvard.edu
Mon Sep 16 22:51:17 BST 2024
NB Arnaud Martin wanted this forwarded to the Heliconius mailing list
From: Samuel Yeaman <samuel.yeaman at ucalgary.ca>
Date: Mon, Sep 16, 2024 at 9:44 AM
Subject: Working group on genomics of repeated adaptation
To: [clipped]
Hi all,
I’m interested in organizing a working group to study the genomic basis
of adaptation using studies of repeated patterns across species – I
think at some point I’ve chatted with you about this (or if I didn’t, I
intended to), so I hope you’re still interested. The big goal is to see
if we can find broad patterns that allow us to test predictions of
population genetic theory, described in more detail here:
https://yeamanlab.weebly.com/repadapt.html
The approach would be to bring together groups of researchers that each
have genomic data on one or a few species in various parts of the big
tree of life that are comparatively well studied (e.g., brassicas,
compositae, mammals, fish, insects, etc), ideally with >5 species per
group, and hopefully many more (as well as additional data in
repositories). Each group will identify a few leaders to conduct the
analysis, which would include calling variants using a common method for
each species in the group, reconstructing orthology relationships,
applying tests to detect signatures of selection within each species
(e.g. selective sweeps, GEA scans), and then making comparisons across
species using PicMin – basically, repeating the methods we used in these
two papers:
https://doi.org/10.1101/2024.04.02.587814
https://doi.org/10.1038/s41559-024-02514-5
A first step is just to see how many genes each group can find that
repeatedly drive adaptation and explore any patterns of enrichment
within these genes, and then start to compare notes among groups and see
if we can say anything more generally about overall patterns that
do/don’t conform to predictions. From there, there are many possible
extensions.
Suitable datasets:
At this point, as the methods rely upon calling orthology using genic
regions, we need to use sequencing datasets that have reads directly in
genic regions (WGS, seqcap, poolseq), with a reasonable quality
annotated reference genome (or one in a closely related species.
Unfortunately RADseq/GBS won’t work well for this, but an eventual goal
could be to update methods to use signatures at the closest-sequenced
site to a gene. At a minimum, there should be enough individuals within
a species to allow detection of selective sweeps, but ideally it would
be nice to also have lots of populations sampled to enable GEA scans.
The aim of this initial meeting is to make connections among
researchers, form groups, and decide on methods and timelines. To give
time to plan ahead, I’m aiming for the first meeting on Tuesday October
22nd at 9am Mountain time/3pm UCT. The meeting will be on zoom (link:
https://ucalgary.zoom.us/j/8570569393) and will be recorded for anyone
that can’t make it.
In preparation for the meeting (and especially if you can’t make the
meeting but would like to participate) please add details of suitable
datasets to this spreadsheet:
https://docs.google.com/spreadsheets/d/1Jr28SWvfVt52pT1lqpfqIQyylyFrzn-NuHGBmX9D-0g/edit?usp=sharing
(not all details need to be filled in now – just getting an estimate of
the number of species in each group and the contributors would be very
helpful)
Eventually, I hope to organize a workshop in Banff where we can get
together and compare results and synthesize/write papers, and perhaps
draft grant applications for deepening/broadening the study.
Importantly: I’ve almost certainly overlooked lots of people that would
have appropriate data and would be interested in contributing to
this…please forward this email to them!
Cheers,
Sam
Ps. I’m also recruiting a PhD student, if you know any interested
candidates:
https://yeamanlab.weebly.com/uploads/5/7/9/5/57959825/phd_position_2024.pdf
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