bpaten
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First complete, gapless sequence of a human genome reveals hidden regions
Parts of the human genome now available to study for the first time are important for understanding genetic diseases, human diversity, and evolution.
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A new way to find genetic variations removes bias from human genotyping
Researchers at the UC Santa Cruz Genomics Institute have demonstrated an effective new tool for mapping genetic variants in sequencing data using ‘pangenomics’ instead of a single reference genome .
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New genome alignment tool empowers large-scale studies of vertebrate evolution
Important new studies of the evolution of birds and mammals relied on Progressive Cactus, a genome alignment tool developed at the UC Santa Cruz Genomics Institute.
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Eleven human genomes sequenced and assembled in nine days
The dawn of good, fast, and cheap human genome assembly has arrived, thanks in part to collaboration and innovation by an international team led by UC Santa Cruz researchers.
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NIH funds new centers to expand and diversify the human reference genome
The UC Santa Cruz Genomics Institute will play a leading role in the ambitious new Human Pangenome Reference Sequence Project.
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Breakthrough leads to sequencing of a human genome using a pocket-sized device
Nanopore sequencing technology, based on concepts pioneered at UC Santa Cruz, has revealed parts of the genome scientists had been unable to sequence before.
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BRCA Exchange aggregates publicly accessible data on breast cancer genes
UC Santa Cruz Genomics Institute led development of a web portal for patients, clinicians, and researchers.
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UC Santa Cruz Genomics Institute partners with Microsoft to accelerate biomedical research
The Microsoft partnership provides the Genomics Institute with access to new compute, data storage, and analysis capabilities.
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Keck Foundation awards UC Santa Cruz $2 million for human genome variation project
The Human Genome Variation Map being developed by the UCSC Genomics Institute will be a valuable new resource for medical researchers.
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UC Santa Cruz to lead effort to build a new map of human genetic variation
The Simons Foundation awarded UCSC up to $1 million to develop a comprehensive Human Genome Variation Map for scientific and medical research
