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The package offers functions to process multiple ChIP-seq BAM files and detect allele-specific events. Computes allele counts at individual variants (SNPs/SNVs), implements extensive QC steps to remove problematic variants, and utilizes a bayesian framework to identify statistically significant allele- specific events. BaalChIP is able to account for copy number differences between the two alleles, a known phenotypical feature of cancer samples.
Package details |
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Author | Ines de Santiago, Wei Liu, Ke Yuan, Martin O'Reilly, Chandra SR Chilamakuri, Bruce Ponder, Kerstin Meyer, Florian Markowetz |
Bioconductor views | Bayesian ChIPSeq Sequencing Software |
Maintainer | Ines de Santiago <inesdesantiago@gmail.com> |
License | Artistic-2.0 |
Version | 1.16.0 |
Package repository | View on Bioconductor |
Installation |
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