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Clinical sequencing of tumor is usually performed on formalin-fixed and paraffin-embedded samples and have many sequencing errors. We found that the majority of these errors are detected in chimeric read caused by single-strand DNA with micro-homology. Our filtering pipeline focuses on the uneven distribution of the artifacts in each read and removes such errors in formalin-fixed and paraffin-embedded samples without over-eliminating the true mutations detected in fresh frozen samples.
Package details |
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Author | Masachika Ikegami [aut, cre] |
Maintainer | Masachika Ikegami <ikegamitky@gmail.com> |
License | MIT + file LICENSE |
Version | 2.1.6 |
URL | https://github.com/MANO-B/MicroSEC/ |
Package repository | View on CRAN |
Installation |
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