𝗧𝗼𝗽 𝟯 𝗧𝗵𝗶𝗻𝗴𝘀 𝘁𝗼 𝗞𝗻𝗼𝘄 𝗔𝗯𝗼𝘂𝘁 𝘁𝗵𝗲 𝗦𝘂𝗿𝗲𝗦𝗲𝗾™ 𝗖𝗟𝗟 + 𝗖𝗡𝗩 𝗩𝟯 𝗣𝗮𝗻𝗲𝗹: 1. Enhanced gene coverage: The panel offers increased coverage for key genes like TP53, BTK, PLCG2, BCL2, and NRAS, aligning with the latest CLL research to provide a more comprehensive understanding of CLL progression. 2. High sensitivity and accuracy: The panel detects low-frequency SNVs and indels down to 1-2.5% VAF and CNVs down to 20% tumour estimation in the 5 most frequently aberrant regions, minimising the risk of missed variant calls. 3. Newly added internal reference DNA: This addition ensures accurate sample characterisation and increased lab efficiency by reducing inter-run variability. Check here for more details 👉 https://lnkd.in/e39WtpjN
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