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Alignments of the parent genes and CG proteins were generated using the Emboss Needle program (http://emboss.sourceforge.net/) with default options.
All pairs of proteins were aligned using the EMBOSS needle program [ 23] and those with more than 30% sequence identity were connected in the paralogy network (see Methods).
We aligned these protein sequences with human protein sequences using the Emboss Needle program (which implements the Needleman-Wunsch algorithm [ 27]) to extract identity, similarity and gap values for each rhesus protein model.
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ORFs were identified by using the EMBOSS software (version 5.0.0; emboss.sourceforge.net).net
GC content was calculated using the EMBOSS geecee program.
(G + C) content was calculated using the eMBOSS geecee program http://inn-temp.weizmann.ac.il/cgi-bin/emboss/geecee[ 63].
Sequences were translated to amino acids using the Emboss Transeq web application [ 87].
Sequence analysis was performed using the Emboss software suite [ 37], Clustal W [ 38] and 3DCoffee [ 39].
Sequence manipulation was carried out using the EMBOSS suite of programmes [ 54].
Introns were assigned by aligning the unigenes with the melon genomic sequence using the Emboss: est2genome [ 105].
Primer pairs were matched against bovine sequence from GenBank, NT and BTGI databases using the EMBOSS [ 26] primersearch tool.
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