COL11A1 mutations in cutaneous squamous cell carcinoma [WES]
收藏NIAID Data Ecosystem2026-03-13 收录
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https://www.ncbi.nlm.nih.gov/sra/SRP326537
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资源简介:
Whole exome sequencing was used to identify frequent COL11A1 mutations in cutaneous squamous cell carcinoma (cSCC). Overall design: Genomic DNA was then isolated from human cSCC using the DNeasy Blood and Tissue kit (Qiagen) according to the manufacturer's instructions. Sequencing libraries were prepared using the Agilent SureSelect Human All Exon V5 (51Mb) target enrichment for whole exome capture and sequenced on the Illumina HiSeq platform with 2x100nt paired-end reads.
创建时间:
2021-10-26



