SuperSAGE is a method of digital gene expression profiling that allows isolation of 26-bp tag fragments from expressed transcripts.
Of these, 2534 are from expressed sequences, equivalent to a non-redundant set of 2328 loci.
The spikes in this T = 3 structure resemble those in T = 4 shells crystallized from expressed protein.
A simple method, using urea at a sub-denaturing concentration, allows unbinding of Cpn60 from expressed protein.
Simple sequence repeats (SSRs) were investigated in the unigene sequences from expressed sequence tags (EST) of sweet orange (Citrus sinensis osbeck), trifoliate orange (Poncirus trifoliata Raf).
Here we present the 3-dimensional structures of the P22 assembly-naive portal formed from expressed subunits (gp1) and the intact tail machine purified from infectious virions.
LKR/SDH was identified from expressed sequence tags (EST) constructed from midgut cDNA libraries of H. longicornis.
In addition to amplification from expressed RNA, this relationship supports the conclusion that the amplicons represent truly expressed transcripts.
All small RNA fragments and the identified orthologs of known miRNAs from miRBase were screened from expressed sequence tag (EST) sequences using SOAP 2.0 program [42].
Evidence from expressed sequence tag, cDNA, genome-wide tiling and splicing microarray datasets demonstrate that alternative splicing occurs in >90% of genes [1] [3].
As each experiment was carried out in triplicate, each gene had three curves from PNA treatment and three curves from expressed antisense experiments.
