@EcoEvoEvoEco @Jenn_Coughlan @DanielBolnick theory here: https://t.co/m8rgxxLTMS if you have 2N haplotypes in panel, the power gains to be had by sequencing greater than 2N coverage are negligible. of course there is no benefit to lowering coverage... but
Next journal club papers: The Statistics of Bulk Segregant Analysis Using Next Generation Sequencing and QTLseqr: An R Package for Bulk Segregant Analysis with Next‐Generation Sequencing https://t.co/F86aP575oY https://t.co/tzpiaXJzf9
Bulk Segregant Analysis Using Next Generation Sequencing http://t.co/9dEPAR6CJ0
Next-Generation Bulk Segregant Analysis http://t.co/oZK9OWPz