ERASE-Seq Ultralow Frequency Variant Detection Analytical Validation
收藏NIAID Data Ecosystem2026-05-25 收录
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资源简介：
The data in this project contain raw Illumina fastq reads representing targeted cancer amplicon sequencing. The DNA samples sequenced are either pure cell line extractions or mixtures of cell lines containing ultralow frequency spiked variants. Detection of the ultralow frequency spiked variants is used to validate the accuracy of the ERASE-Seq method and algorithm in ultralow frequency SNV and indel detection.
创建时间：
2018-01-30
