Blog
This blog features voices from PacBio — and our partners and colleagues — discussing the latest research, publications, and updates about HiFi sequencing.
Blog
New Isoform-Level Transcriptome Reference Helps Shrimp Industry Ward Off Disease
One of the fastest growing global foods is also one of its most vulnerable. Without an adaptive immune system, the Pacific white shrimp, Litopenaeus vannamei, rely on cellular and humoral…
Two New Reference Genomes Expand Potential for Millet as Super Cereal Crop
The modern world might benefit from a return to our ancient roots by expanding the cultivation of one of the first domesticated crops, broomcorn millet. Foodies will appreciate that the…
New Progress in Representing Population Diversity in Human Genomes
We’re seeing real progress in efforts to better characterize genomic population diversity. That’s particularly good news in light of mounting concerns about the implications of having genomic databases that over-represent…
From the Smallest Organisms to the Most Complex, the Future is Bright for Plant & Animal Sequencing
For the thousands of scientists who attended The Plant and Animal Genome Conference in San Diego this January, the sentiment seemed to be “ask not if PacBio is for you,…
AGBT 2019: First Look at Early Access Results from the Sequel II System
The PacBio team was honored to have the opportunity to give several talks at this year’s Advances in Genome Biology & Technology conference. If you weren’t able to be there,…
GIAB Expands Variant Call Sets with SMRT Sequencing Results
You may have missed last week’s Advances in Genome Biology & Technology conference in sunny Marco Island, Fla., but you definitely shouldn’t miss the two posters presented there by Justin…
Scientists Uncover Epilepsy-Causing Structural Variant with SMRT Sequencing
A new publication in the Journal of Human Genetics describes an impressive effort to identify the pathogenic variant causing progressive myoclonic epilepsy in two siblings. The scientific team used SMRT…
Unsolved Mysteries: Sequencing to Solve Neurologic Disease with Structural Rearrangements
Please join us in congratulating Kristen Sund from Cincinnati Children’s Hospital Medical Center for winning our 2018 Structural Variation SMRT Grant Program! Her proposal to use SMRT Sequencing to pinpoint…
Asian Aquaculture Industry Benefits From Two New Genome Assemblies
With their large brains, sophisticated sense organs and complex nervous systems, cephalopods could teach us a thing or two about learning, memory, and adaptability. But despite their evolutionary, biological, and…
Service Providers: Boost Your Reach with a Simple Marketing Strategy
Getting the word out about your services is a surefire way to get more interest — and ultimately more projects — into your pipeline. The good news is, it doesn’t…
Scientists Produce Valuable New Human Structural Variation Resource Using SMRT Sequencing
In an effort to produce a comprehensive list of structural variants in the human genome, scientists from the University of Washington, the University of Chicago, Washington University, and Ohio State…
Q&A: Scientists Discovered Somatic Recombination in the Brain. Now What?
The recent Nature paper describing the first evidence of somatic gene recombination in the human brain has been getting so much attention that we went back to the lab’s PI…
One For All: HiFi Long Reads for de Novo Assembly and Comprehensive Variant Detection
UPDATED August 12, 2019 This paper is now published in Nature Biotechnology. ORIGINAL POST January 15, 2019 We’re excited to report on new SMRT Sequencing advances that will ultimately help…
Webinar Recap: SMRT Sequencing offers Many Advantages for Microbial Research
According to many, PacBio is the new “gold standard” in microbial sequencing. Chief Scientific Officer Jonas Korlach notes that its ability to simultaneously provide long sequencing reads (genome contiguity), high…
Scientists Resolve Epilepsy-Causing Repeat Expansion with Sequel System
Scientists in Japan report using the unique properties of SMRT Sequencing to detect a structural variant (SV) responsible for a hereditary form of epilepsy. The 4.6 kb intronic repeat insertion…