Additional file 3.
Transcripts with different representation between male and female libraries. To calculate the fold difference in the representation of unigenes between the two libraries, we used the number of reads from each library normalized by the library size (in number of reads) as a measure of the transcript abundance. Of the 101 unigenes differently represented, 57 was either male or female specific and the fold change was calculated assuming a value of 1 in the library with no reads. Positive and negative values represent a highest number of reads in the female and male libraries, respectively. Only unigenes represented by at least 20 reads were included.
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Carvalho et al. BMC Genomics 2010 11:695 doi:10.1186/1471-2164-11-695