Publication & Citation Trends
Publications
0 total
Clinical experience of using integrated whole genome and transcriptome sequencing as a framework for pediatric and adolescent acute myeloid leukemia diagnosis and risk assessment
Cited by 1
Semantic Scholar
Integrative proteogenomics and forward genetics reveals a novel mitotic vulnerability in triple-negative breast cancer.
Cited by 1
Semantic Scholar
CanID: a robust and accurate RNAseq Expression-based diagnostic classification scheme for pediatric malignancies
Cited by 0
Semantic Scholar
Integrated Whole Genome and Transcriptome Sequencing as a Framework for Pediatric and Adolescent AML Diagnosis and Risk Assessment
Cited by 1
Semantic Scholar
Comparison of Molecular Testing Methodologies for CIC-Rearranged Sarcomas.
Cited by 4
Semantic Scholar
Fast and sensitive detection of targeted gene fusions using frequency minimizers and fuzzy pattern matching with Fuzzion2
Cited by 1
Semantic Scholar
CanID: A Robust and Accurate RNA-seq Expression-based Diagnostic Classification Scheme for Pediatric Malignancies.
Cited by 0
Semantic Scholar
Abstract 7178: Advancing WGS and WTS diagnostic testing for pediatric leukemia: fast-tracking CNV, ploidy, and fusion oncogene detection in 5 days
Cited by 0
Semantic Scholar
Research Topics
Cancer Genomics and Diagnostics
(140)
RNA modifications and cancer
(51)
Genetic factors in colorectal cancer
(42)
Genomics and Rare Diseases
(40)
Genomics and Phylogenetic Studies
(32)
Affiliations
Università Cattolica del Sacro Cuore
Broad Institute
Human Genome Sciences (United States)
University of North Carolina at Chapel Hill
James S. McDonnell Foundation