Clinical sequencing of tumor is usually performed on formalin-fixed and paraffin-embedded (FFPE) 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 microhomology. Our filtering pipeline focuses on the uneven distribution of the artifacts in each read and removes such errors in FFPE samples without over-eliminating the true mutations detected in fresh frozen samples.
Version: | 1.1.3 |
Depends: | R (≥ 3.4.0) |
Imports: | tidyr, openxlsx, data.table, R.utils, stringr, magrittr, dplyr, gtools, Biostrings, GenomicAlignments, Rsamtools, GenomeInfoDb, BiocGenerics |
Suggests: | BSgenome.Hsapiens.UCSC.hg38, BSgenome.Hsapiens.UCSC.hg19, BSgenome.Mmusculus.UCSC.mm10, knitr, rmarkdown |
Published: | 2020-12-02 |
Author: | Masachika Ikegami [aut, cre] |
Maintainer: | Masachika Ikegami <ikegamitky at gmail.com> |
BugReports: | https://github.com/MANO-B/MicroSEC/issues |
License: | MIT + file LICENSE |
URL: | https://github.com/MANO-B/MicroSEC/ |
NeedsCompilation: | no |
Materials: | README |
CRAN checks: | MicroSEC results |
Reference manual: | MicroSEC.pdf |
Vignettes: |
my-vignette |
Package source: | MicroSEC_1.1.3.tar.gz |
Windows binaries: | r-devel: MicroSEC_1.1.3.zip, r-release: MicroSEC_1.1.3.zip, r-oldrel: MicroSEC_1.1.3.zip |
macOS binaries: | r-release: MicroSEC_1.1.3.tgz, r-oldrel: not available |
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