Research. Insights. Real talk on genomics.
Science-first content from the researchers building the tools.
How to Transition from SNP Arrays to Sequencing in Your Breeding Program
SNP arrays have served plant breeding well. But fixed marker sets can't detect structural variants, rare alleles, or complex polyploid regions. Here's what the transition to long-read sequencing actually looks like and why you don't need to rebuild your program to start.
Your Revio Is Ready. Is Your Lab?
HiFi library prep for a PacBio Revio takes a full day of bench time for 8 samples. At scale, it's weeks. Here's what in-house prep is actually costing your lab.
What Short-Read Sequencing is Costing Your Breeding Program, and What the Data Shows
At matched sequencing depth, short-read low-pass sequencing covered 17% of the peanut genome. Long-read low-pass sequencing covered 55%. A head-to-head study of 127 breeding lines shows what plant breeders are missing with current methods — and what changes when you switch.
You Don't Have a Data Problem. You Have a Resolution Problem.
Over the past decade, plant breeding has undergone a data revolution. Sequencing costs have dropped, datasets have grown, and genomic tools are now embedded in modern breeding programs.
And yet—many of the most important traits remain frustratingly difficult to resolve.
Why?
The Tone Knob Nobody Touches
I spent 30 years writing songs with the tone knob open. I never thought I needed to do anything different…
We Launched, We Delivered, and We're Grateful: A Note From Veil's President
The team at Veil has a big debt of gratitude we'd like to share with the world, and we want to start by saying thank you. Thank you to the investors, clients, colleagues, and friends who have put their faith in us and the mission we are on…