Additional file 5.
SNVs detected by mapping SOLiD sequences against melon transcriptome. All SNVs detected in all eight resequenced pools are included, their position in the reference transcriptome available in http://melogene.net webcite, their allelic frequency in each group are detailed. Alleles in reads from genotypes previously sequenced with Sanger and 454 are also indicated.
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Blanca et al. BMC Genomics 2012 13:280 doi:10.1186/1471-2164-13-280