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. 2007 May 9;8:113. doi: 10.1186/1471-2164-8-113

Table 1.

Bioinformatics scheme for identifying novel transcripts

Steps in the scheme Number of sequences
Removed Remaining
Starting set of 5' placenta ESTs 12,614
PipeBLASTN (automated BLASTN analysis) 10,235 2,379
In silico extension of 5' ESTs with public cattle ESTs, followed by PipeBLASTN 581 1,798
3' reads from single-pass sequencing using anchored oligodT primer 618 1,180
PipeBLASTN of 3' reads 404 776
Assembly of 3' and extended 5' mates NAa 493
Full-clone sequencing of unassembled 3' ESTs NA 283
In silico extension of 493 mate-pairs followed by PipeBLASTN 171 322
In silico extension of 283 primer-walked clones, followed by PipeBLASTN 232 51
Working set of divergent homologs and novel transcripts (322+51) NA 373
TBLASTX against UniGene databases to separate novel transcripts from divergent homologs 75 298
In silico extension followed by PipeBLASTN using updated databases to yield final set of NTs. 134 164
Screening for internal poly A tracts 73 91

a NA; not applicable.