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Reproducibility of variant calls in replicate next generation sequencing experiments

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NIAID Data Ecosystem2026-03-10 收录
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In this study, we examined the reproducibility of nucleotide variant calls in replicate sequencing experiments of the same genomic DNA. We performed targeted sequencing of all known human protein kinase genes (kinome) (~3.3 Mb) using the SOLiD v4 platform. Seventeen breast cancer samples were sequenced in duplicate (n=14) or triplicate (n=3) to assess concordance of all calls and single nucleotide variant (SNV) calls.EGA study EGAS00001000826

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2017-07-26
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