Search-and-replace genome editing without double-strand breaks or donor DNA | Nature
ClinGen — The Clinical Genome Resource | NEJM
Pecan PIE - St. Jude Cloud Documentation
![PDF] Development of a Comprehensive NGS Workflow for the Analysis of Tumor BRCA1 and BRCA2 Mutations and Large Rearrangements | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/c812052ee66937dd7c55bc0ab860a79cc9d29a6c/2-Figure1-1.png "PDF] Development of a Comprehensive NGS Workflow for the Analysis of Tumor BRCA1 and BRCA2 Mutations and Large Rearrangements | Semantic Scholar")
PDF] Development of a Comprehensive NGS Workflow for the Analysis of Tumor BRCA1 and BRCA2 Mutations and Large Rearrangements | Semantic Scholar
Simple ClinVar results section according to the three types of input... | Download Scientific Diagram
Comparison of locus-specific databases for BRCA1 and BRCA2 variants reveals disparity in variant classification within and among databases | SpringerLink
Screenshot from ClinVar: a consolidated view of interpretations for a... | Download Scientific Diagram
New & Improved ClinVar Annotations - VarSeq Software
ClinVar - ClinGen | Clinical Genome Resource
Enabling openness of valuable information resources: Curbing data subtractability and exclusion - Vassilakopoulou - 2019 - Information Systems Journal - Wiley Online Library
IJMS | Free Full-Text | Consolidated BRCA1/2 Variant Interpretation by MH BRCA Correlates with Predicted PARP Inhibitor Efficacy Association by MH Guide | HTML
Concordance of Genomic Variants in Matched Primary Breast Cancer, Metastatic Tumor, and Circulating Tumor DNA: The MIRROR Study | JCO Precision Oncology
BRCA Challenge: BRCA Exchange as a global resource for variants in BRCA1 and BRCA2
Sources of discordance among germ-line variant classifications in ClinVar | Genetics in Medicine
Sources of discordance among germ-line variant classifications in ClinVar | Genetics in Medicine
ClinGen — The Clinical Genome Resource | NEJM
Pathogenic single nucleotide variants in BIC and ClinVar | Download Table
Comparative analysis of BRCA1 and BRCA2 variants of uncertain significance in patients with breast cancer: a multifactorial probability-based model versus ACMG standards and guidelines for interpreting sequence variants | Genetics in Medicine
ClinGen — The Clinical Genome Resource | NEJM
IJMS | Free Full-Text | Consolidated BRCA1/2 Variant Interpretation by MH BRCA Correlates with Predicted PARP Inhibitor Efficacy Association by MH Guide | HTML
