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Our method integrates information from all sequenced samples, thus avoiding loss of alleles due to low coverage. Moreover, it increases the statistical power to uncover sequencing or alignment errors <doi:10.1093/plphys/kiad191>.
Package details |
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Author | Rafael Campos-Martin [cre] (<https://orcid.org/0000-0002-1395-8571>), Sophia Schmickler [aut], Manish Goel [ctb], Korbinian Schneeberger [aut], Achim Tresch [aut] |
Bioconductor views | GenomeAnnotation HiddenMarkovModel Sequencing |
Maintainer | Rafael Campos-Martin <rfael.mpi@gmail.com> |
License | GPL (>= 2) |
Version | 2.1.0 |
Package repository | View on CRAN |
Installation |
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