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Resolution: standard / high Figure 2.
Overview of probe design: genomic coordination of TSSs and CAGE-TSSchip probes. The
upper four tracks are an arrangement example of full-length transcripts (cDNA) and
5'-ends of transcripts derived from various methods (cap analysis gene expression
[CAGE], 5'-expressed sequence tag [EST], and 5'-end of gene identification signature/gene
signature cloning [4]). Tag clusters (TC; green arrow) are the overlapping regions
of the 5'-ends. The most frequent transciption start site (TSS) for each TC is the
representative position (vertical line from TC arrows). Fragments for the probe design,
of 120-nucleotide long genomic sequences, starts from the representative position
of each TC fragment, shown by cyan arrows. If the fragment overlaps the 5'-end of
any exon-intron junction (diamond of cDNA and 5'-EST transcripts), the fragment skips
the intron to the next exon. According to the Agilent probe design service, the 60-nucleotide
appropriate region within each fragment would then be suggested for array probes (probe;
blue arrows). Details of probe preparation are available in Additional data file 8.
Katayama et al. Genome Biology 2007 8:R42 doi:10.1186/gb-2007-8-3-r42 |