1/6 @illumina just announced the $200 whole genome 🧬 The most powerful machines in the Novaseq X series can produce 20,000 genomes a year, so how can we make sense of all that data in #cancerresearch? COSMIC has the answers 💡 #IGF
2/6 🧬Rapidly prioritise genes which have evidence of a causal role in cancer with #COSMICCGC, and understand their biological role via our Hallmarks Annotation: bit.ly/3SFN1SO
3/6 🚘 Separate driver from passenger mutations with #COSMICCMC - where mutations are classified into tiers based on bioinformatic analysis from sources such as @clinvar #DnDs ratios and core-COSMIC data: bit.ly/3y5XoaO
4/6 💊 Track progress of drug trials or find out if there’s already a drug available to target a specific mutation with #COSMIC_Actionability : bit.ly/3LVjDWw
5/6 💊💻 No drugs available? Visualise the consequences of specific mutations in a 3D protein model and even view ‘druggability scores for pockets’ with #COSMIC3D: bit.ly/COSMIC3D 
6/6 With over 23,000,000 genomic variants from nearly 30,000 publications. COSMIC is the world’s most comprehensive database of somatic mutations in cancer🧬The perfect accompaniment to analyse any WGS samples, and boost the potential of your research 🚀
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