TY - JOUR A1 - Osato, Naoki A1 - Itoh, Masayoshi A1 - Konno, Hideaki A1 - Kondo, Shinji A1 - Shibata, Kazuhiro A1 - Carninci, Piero A1 - Shiraki, Toshiyuki A1 - Shinagawa, Akira A1 - Arakawa, Takahiro A1 - Kikuchi, Shoshi A1 - Sato, Kouji A1 - Kawai, Jun A1 - Hayashizaki, Yoshihide T1 - A Computer-Based Method of Selecting Clones for a Full-Length cDNA Project: Simultaneous Collection of Negligibly Redundant and Variant cDNAs Y1 - 2002/07/01 JF - Genome Research JO - Genome Research SP - 1127 EP - 1134 DO - 10.1101/gr.75202 VL - 12 IS - 7 UR - http://genome.cshlp.org/content/12/7/1127.abstract N2 - We describe a computer-based method that selects representative clones for full-length sequencing in a full-length cDNA project. Our method classifies end sequences using two kinds of criteria, grouping, and clustering. Grouping places together variant cDNAs, family genes, and cDNAs with sequencing errors. Clustering separates those cDNA clones into distinct clusters. The full-length sequences of the clones selected by grouping are determined preferentially, and then the sequences selected by clustering are determined. Grouping reduced the number of rice cDNA clones for full-length sequencing to 21% and mouse cDNA clones to 25%. Rice full-length sequences selected by grouping showed a 1.07-fold redundancy. Mouse full-length sequences showed a 1.04-fold redundancy, which can be reduced by ∼30% from the selection using our previous method. To estimate the coverage of unique genes, we used FANTOM (Functional Annotation of RIKEN Mouse cDNA Clones) clusters (the RIKEN Genome Exploration Research Group 2001). Grouping covered almost all unique genes (93% of FANTOM clusters), and clustering covered all genes. Therefore, our method is useful for the selection of appropriate representative clones for full-length sequencing, thereby greatly reducing the cost, labor, and time necessary for this process.[The programs used in this paper are available online at http://genome.gsc.riken.go.jp/software/2C.] ER -