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. 2016 Nov 28;45(5):e34. doi: 10.1093/nar/gkw1086

Figure 1.

Figure 1.

The individual steps that make up the sCNAphase workflow. (A) Each panels shows an individual process used by sCNAphase to characterize the copy number profile from matched tumor and normal pairs. (B) The B-allele frequencies (BAFs) from a region of chromosome 8 from the HCC1143 breast cancer cell-line. (C) The application of phasing to the BAF data makes it possible to identify parental-haplotype frequencies (PHFs), regions composed of 40 adjacent germline, heterozygous single nucleotide polymorphisms (SNPs). Each PHF increase the power of this analysis and makes it possible to better reflect the copy number profile of this region. (D) Application of the sCNAphase pipeline to the phased data, calls specific copy number changes.