ANNOVAR (3): 更新COSMIC 数据库(v70+) - 郑泽鑫的博客
GenIO
ClinGen Allele Registry links information about genetic variants - Pawliczek - 2018 - Human Mutation - Wiley Online Library
GitHub - fanyucai1/annovar
WGSA: an annotation pipeline for human genome sequencing studies | Journal of Medical Genetics
Quick Start-Up Guide - ANNOVAR Documentation
PPLine: An Automated Pipeline for SNP, SAP, and Splice Variant Detection in the Context of Proteogenomics | Journal of Proteome Research
CSTAR ::
ANNOVAR - Wikipedia
From raw reads to variants - ppt download
OpenVar: functional annotation of variants in non-canonical open reading frames | Cell & Bioscience | Full Text
Please update cosmic90 prepare_annovar_user.pl · Issue #77 · WGLab/doc- ANNOVAR · GitHub
Quick Start-Up Guide - ANNOVAR Documentation
COSMIC - QIAGEN Digital Insights
Preparation for Somatic Mutation Annotator
Workflow for bioinformatics analysis of the DNA sequencing data.... | Download Scientific Diagram
Tutorial
Cosmic Annotation is not parsed correctly · Issue #83 · WGLab/doc-ANNOVAR · GitHub
Frontiers | CCAS: One-stop and comprehensive annotation system for individual cancer genome at multi-omics level
Correction: Whole-exome sequencing of BRCA-negative breast cancer patients and case–control analyses identify variants associated with breast cancer susceptibility,Human Genomics - X-MOL
Frontiers | Identifying Actionable Variants Using Capture-Based Targeted Sequencing in 563 Patients With Non-Small Cell Lung Carcinoma
New Release: COSMIC v97 and Actionability v7 Now Available - QIAGEN Digital Insights
ANNOVAR - Wikipedia
ANNOVAR & web-ANNOVAR Software | QIAGEN
ANNOVAR - Wikipedia
Cosmic v90 normalization MNVs · Issue #132 · WGLab/doc-ANNOVAR · GitHub
Example: Analysis of the distribution of somatic variants in cancer with respect to 3D protein structure and interacting interfaces
