From: Jose B. <jb...@bt...> - 2009-09-18 11:15:37
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Hi: I've aligned some sanger and solexa reads to a reference genome with bwa. I've merged, sorted and pileuped the alignments. Now I have the bam and the pileup files. I would like to obtain a caf like alignment file (or a file with such information). The information not present in the pileup file is the name, nucleotide and quality of each individual read that contribute to the consensus. That information is very useful when reads originated from several individuals/samples are aligned. Is that posible? If it is not posible, could you give me some direction on how could I program such tool? Best regards, -- Jose M. Blanca Postigo Instituto Universitario de Conservacion y Mejora de la Agrodiversidad Valenciana (COMAV) Universidad Politecnica de Valencia (UPV) Edificio CPI (Ciudad Politecnica de la Innovacion), 8E 46022 Valencia (SPAIN) Tlf.:+34-96-3877000 (ext 88473) |