What does short-read epigenomics miss?
A study using Fiber-seq on human brain tissue found ~20,000 accessible chromatin regions missed by short-read methods. Read our new blog to learn more⤵️
ow.ly/fqSm50Z1kzz#FiberSeq#Epigenomics
We're headed to San Diego for #PAG2026! 🌴
Visit booth 329 to talk with EpiCypher about Fiber-seq – our next-gen single-molecule chromatin profiling platform.
Let’s decode chromatin, one molecule at a time 🧬
#Epigenetics#Fiberseq#Genomics
Huge thanks to everyone who visited us on Day 1 of #ASHG2025! 👏 If you haven’t yet, swing by Booth 530 today to explore Fiber-seq – a multiomic long-read tech to co-profile chromatin, DNA methylation, and footprints.
#Epigenetics#FiberSeq#ASHG
Heading to #ASHG2025? Don’t miss Emily Madden’s talk:
🧬 “Unraveling Regulatory Architecture in Complex Genomic Regions Using Fiber-seq”
🗓️ Fri, Oct 17 | 10:15am ET
📍 CoLab Theater 1 (PacBio)
#Epigenetics#Fiberseq#Chromatin
Just announced: CUTANA™ Fiber-seq — a game-changing platform for multiomic profiling of chromatin accessibility, DNA methylation, protein footprints, and genetic variants in a single assay.
🔗 epicypher.com/resources/blog…#Epigenetics#Fiberseq#Chromatin
Going to Epigenetic Variation in Barcelona? 🇪🇸
Catch Dr. James Anderson’s talk on Fiber-seq 🧬, a multi-omic LRS method revealing chromatin, TFs, DNAme and haplotypes in one assay.
📍 Aug 14 | 🕘 9am CEST
#Epigenetics#FiberSeq#LRS
#PacBio is heading to #AGBT25 with updates on HiFi sequencing, Vega, and new applications like FiberSeq and DAF-seq. Learn how these innovations, along with the latest in SPRQ chemistry, are shaping the future of genomics. See you there! #AGBT2025