Researchers at UC Santa Cruz introduce the first-ever method for analyzing RNA sequencing data genome-wide using a “pantranscriptome.”

The UCSC Genome Browser is now part of the first list of Global Core Biodata Resources—a collection of 37 resources whose long-term funding and sustainability is critical to life science and biomedical research worldwide.

A new study led by scientists at UC Santa Cruz and published in the journal Proceedings of the National Academy of Sciences (PNAS) points to introners, one of several proposed mechanisms for the creation of introns, as an explanation for the origins of most introns across species.

A team of engineers and scientists at UC Santa Cruz has developed a new method for remote automation of the growth of cerebral organoids – miniature, three-dimensional models of brain tissue grown from stem cells.

As detailed in new research, UC Santa Cruz researchers have developed a method for using remote-controlled, internet-connected microscopes to enable students anywhere in the world to participate in designing and carrying out biology experiments.

Assistant Professor of Biomolecular Engineering Daniel Kim won a four-year, $792,000 Research Scholar award from the American Cancer Society to support his work in developing RNA liquid biopsy technology to diagnose cancer early on.

UC Santa Cruz Baskin School of Engineering Professor Richard (Ed) Green was a major contributor to the Neanderthal Genome Project , the leader of which, Svante Pääbo, received the 2022 Nobel Prize in Physiology or Medicine.

UC Santa Cruz Assistant Professor of Biomolecular Engineering and Associate Director for Human Pangenomics at the UCSC Genomics Institute Karen Miga joined former President Bill Clinton, U2 lead singer Bono, and Director-General of the World Health Organization (WHO) Tedros Ghebreyesus to talk about the greatest health challenges and opportunities the world is currently facing. 

This Tuesday, September 20 at 1:30 PST, Karen Miga will speak during the conference’s closing plenary session, joining Bill Clinton, Lin Manuel Miranda, Dolores Huerta, and more.

The UC Santa Cruz Genomics Institute will partner with California State University, Monterey Bay (CSUMB) and the University of Puerto Rico, Río Piedras Campus to mentor and provide genomics research experience for students from these two hispanic-serving institutions.

More than a quarter century since the first patents were filed, the UCSC researchers who pioneered nanopore sequencing reflect on the impact of their invention

An analysis of millions of SARS-CoV-2 genomes finds that recombination of the virus is uncommon, but when it occurs, it is most often in the spike protein region, the area which allows the virus to attach to and infect host cells.

A new study finds that a key genetic mutation that occurs early on in cancer alters RNA “dark matter” and causes the release of previously unknown RNA biomarkers for cancer early detection.

A new program out of the UC Santa Cruz Genomics Institute involves students in an effort to measure changes in biodiversity and ultimately prevent them.

The California Conservation Genomics Project (CCGP) is a state-funded initiative with a single goal: to produce the most comprehensive, multispecies genomic dataset ever assembled to help manage regional biodiversity.

10 million sequences of COVID-19’s genomic code have now been organized into a phylogenetic tree in the UC Santa Cruz SARS-CoV-2 Browser, which is the largest tree of genomic sequences of a single species ever assembled.

Karen Miga, assistant professor of biomolecular engineering at UC Santa Cruz, was named one of the 100 most influential people of 2022 by TIME. The honor was announced on May 23.

The UC Santa Cruz Genomics Institute is collaborating with Amazon Web Services (AWS) to allow researchers to quickly and efficiently execute bioinformatics pipelines on AWS’s global cloud infrastructure.

As COVID-19 continues to mutate, software developed and maintained at the University of California, Santa Cruz’s Genomics Institute will now be at the core of the primary tool used by health officials worldwide to track the spread of variants in their community. It is now the default software behind the ubiquitously used tool Pangolin, replacing previous software to more accurately assign genomic samples of COVID-19 to a known branch on the virus’s family tree.  

Parts of the human genome now available to study for the first time are important for understanding genetic diseases, human diversity, and evolution.