摘要
To obtain a primary overview of gene diversity and expression pattern inLycoris longituba, 4,992 ESTs (Expressed Sequence Tags) from L. longituba bud were se-quenced and4,687 cleaned ESTs were used for gene expression analysis. Clustered by the PHRAP program, 967contigs and 1,343 singlets were obtained. Blast search showed that 179 contigs and 227 singlets(totally 1,066 ESTs) had homologues in GenBank and 3,621 ESTs were novel.
To obtain a primary overview of gene diversity and expression pattern inLycoris longituba, 4,992 ESTs (Expressed Sequence Tags) from L. longituba bud were se-quenced and4,687 cleaned ESTs were used for gene expression analysis. Clustered by the PHRAP program, 967contigs and 1,343 singlets were obtained. Blast search showed that 179 contigs and 227 singlets(totally 1,066 ESTs) had homologues in GenBank and 3,621 ESTs were novel.
基金
Hi-tech Research &Development Program of China (863 Program, No. 2002AA241051) and Science & Technology Program for Agriculture Development of Shanghai.
