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We aligned the reads against the sesame reference genome sequence and only the uniquely mapped reads (70.2% of raw reads) in the reference genome (in total 1,269-fold read depth) were used for SNP calling. |
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We aligned the reads against the sesame reference genome sequence and only the uniquely mapped reads (70.2% of raw reads) in the reference genome (in total 1,269-fold read depth) were used for SNP calling. ÎÒÃǽáºÏÁËÖ¥ÂéµÄ²Î¿¼»ùÒò×éÐòÁеĶÁÂ룬£¨·¢ÏÖ£©²Î¿¼»ùÒòÖУ¨ËùÓÐ1269±¶¶ÁÈ¡Éî¶ÈÖУ©£¬Ö»ÓÐÌØÊâ»æÖÆµÄ¶ÁÂ루Ôʼ¶ÁÂëµÄ70.2%£©¿ÉÒÔ±»ÓÃÓÚSNP¼ÆËã |
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