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Old 10-16-2021, 01:23 PM   #1
Location: San Francisco, CA

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Post Benchmark data sets and best practices for WGS/WES somatic mutation detection

The FDA-led MAQC-IV/SEQC2 Consortium has published the data descriptor paper, i.e., Zhao Y. et al. Sci Data (2021), detailing the multi-center multi-platform whole-genome and whole-exome sequencing data sets for the breast cancer cell line HCC1395 and and its B lymphocyte-derived matched normal HCC1395BL. The genomic DNA was produced in a single batch by ATCC to ensure sample homogeneity. The following are some of the Consortium's papers that used those data sets:

Find all of SEQC2's publications:

Last edited by lethalfang; 11-09-2021 at 11:32 AM.
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cancer ngs, cancer sequencing, somatic mutations

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