We still have space available in our upcoming Variant Detection workshop (virtual with live instruction – Jan. 27–29). This hands-on workshop introduces the core concepts and tools used to identify and analyze genetic variants from high-throughput sequencing data.

Topics include Linux and high-performance computing (HPC) basics, high-throughput sequencing fundamentals, reference alignment and quality control, variant calling models and pipelines (GATK, Freebayes, BCFtools), and variant call filtering, comparison, and annotation. This workshop is designed for beginners—no prior bioinformatics experience required.

Learn more & register here: https://bioinformatics.uconn.edu/cbc-workshops/

WHERE: Virtual (MS Teams | recordings distributed)

WHEN: 10:00 AM – 2:00 PM EST

COST: $400 (University of Connecticut affiliates, including UConn Health) | $500 (external participants)

Registration is first come, first served. No application process.

Questions? E-mail cbcsupport@helpspotmail.com