This population genetics study used Terra to identify mitochondrial variants in 56K+ whole genomes from the gnomAD database using a scalable GATK workflow.
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End-to-end testing of tools and pipelines in practice and at scale; inspired by “Ten simple rules for large-scale data processing” (Fungtammasan 2022).
This prostate cancer study used Terra to process exome sequencing and single-cell RNAseq data with automated workflows.
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Lead Educator Robert Majovski presents a listicle of 8 key resources that can help Terra newcomers and veterans alike get the most out of the Terra platform.
Samantha Zarate of the Schatz Lab takes us behind the scenes of the large-scale analysis that demonstrated the benefits of the new T2T-CHM13 reference genome for variant calling.
Dr. Kiran Garimella gives an overview of MAS-ISO-seq, a new method for generating a lot more data per run with long-read sequencing technologies such as PacBio, and shares a workspace that demonstrates the method's data processing.
An overview of data and analysis resources provided by the BRAIN Initiative Cell Census Network (BICCN) via the Neuroscience Multi-omic Archive (NeMO) and Terra
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