The following articles provide background information about Personalis’ technologies and founders. For additional information, see our extensive list of peer-reviewed publications.
In a report in Genome Medicine last week, researchers from human genome sequencing firm Personalis shared results from their comparison of different tools for translating genomic variant data into a syntax that can be referenced across legacy transcriptomic or proteomic reports. Overall, they found there was "significant inconsistency," both from tool to tool and in comparison to existing databases.
Personalis to support ongoing research efforts to demonstrate that Argos’ lead product candidate, rocapuldencel-T, specifically targets patients’ tumor-specific neoantigens without the need to identify them first.
"This effort will help us continue to hone the neoantigen prediction methods we are using in our neoantigen-based personalized cancer vaccines partnerships and immunotherapy diagnostics," Dr. Richard Chen, Personalis' chief scientific officer said in an email to the San Francisco Business Times. "This work has the potential to be truly transformative.”
Quest Diagnostics to Enhance Diagnosis of Pediatric Neurological Disorders with Exclusive Whole Exome Sequencing from Personalis
Proprietary Neurome™ service provides insight into the genetic causes of neurological disorders so parents and health care providers can develop personalized care strategies
Next-generation sequencing has facilitated an explosion in clinical genetic testing, and for some patients with unknown disorders for which there were previously no genetic tests available, exome sequencing is now an option.