Genome Nexus (1) aggregates variant information from sources that are relevant to cancer research and clinical applications, (2) allows high-performance programmatic access to the aggregated data via ...
Gene annotation is one of the core mechanisms through which we decipher the information that is contained in genome sequences. Gene annotation is complicated by the existence of 'transcriptional ...
Interpretation of genomic variants in tumor samples still presents a challenge in research and the clinical setting. A major issue is that information for variant interpretation is fragmented across ...
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