Combining RT-PCR-seq and RNA-seq to catalog all genic elements encoded in the human genome

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Figure 8.
Figure 8.

Sensitivity of the RT-PCR-seq method. The RT-PCR-seq validation rates of exon–exon junctions are shown as a function of the abundance of the targeted transcript isoforms. The latter was ascertained by counting the number of validating reads detected in HBM RNA-seq experiments. The results obtained for the seven tissues used in both HBM RNA-seq and GENCODE RT-PCR-seq were considered (brain, heart, lung, testis, liver, kidney, and skeletal muscle) either separately (A) or merged together (B).

This Article

  1. Genome Res. 22: 1698-1710

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