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@pwhmolhaem has been a member of Linktree for 3 years and joined in October 2022. Besides social media accounts, pwhmolhaem has populated their site with CUHK OneDrive, NGS QAP Evaluation Report, GNS testcode, GenQA- Genomics Quality Assessment Authentication, QIAGEN Digital Insights – Login (QCI), Sequence Variant Interpretation - ClinGen | Clinical Genome Resource, VarSome The Human Genomics Community, ANNOVAR Documentation, Myeloid Malignancy Variant Curation Expert Panel - ClinGen | Clinical Genome Resource, Evidence Repository - Clinical Genome Resources, Cancer Hotspots, Search Variants in ClinGen Allele Registry, CanVIG-UK Gene Specific Recommendations | CanGene-CanVar, The TP53 Database | ISB-CGC, (Germline) LOVD - An Open Source DNA variation database system, COSMIC - Catalogue of Somatic Mutations in Cancer, cBioPortal for Cancer Genomics, LitVar2 - NCBI - NLM - NIH, bibliome.ai, dbSNP - NCBI, gnomAD, ChimerDB, Mitelman Database: Chromosome Aberrations and Gene Fusions in Cancer, FusionGDB 2.0: fusion gene annotation update aided by deep learning, FGviewer: a tool for visualizing functional features of human fusion gene, fusioncatcher [description], Star Fusion [annots], Human hg19, Human hg38.