非实体 发表于 2025-3-26 23:20:51
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Statistical Methods for the Analysis of Next Generation Sequencing Data from Paired Tumor-Normal Sarutinized with unprecedented resolution and sensitivity. In this chapter, we discuss statistical methods that have been proposed to detect somatic variations at the DNA level using paired tumor and normal sequencing data, including single nucleotide alterations (SNAs) and copy number alterations (CN教唆 发表于 2025-3-27 08:56:57
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Somnath Datta,Dan NettletonProvides statistical tools for working with the latest research data in NGS.Contains chapters written by leading statisticians in the field of NGS.Useful for students and researchers that work in biomhurricane 发表于 2025-3-27 15:50:04
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https://doi.org/10.1007/978-3-319-07212-8Copy Number Variation; DNA; Genomics; Isoform Expression Detection; RNA; Sequencing Data不整齐 发表于 2025-3-28 07:10:22
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