The use of exome capture RNA-seq for highly degraded RNA with application to clinical cancer sequencing

(Downloading may take up to 30 seconds. If the slide opens in your browser, select File -> Save As to save it.)

Click on image to view larger version.

Figure 2.
Figure 2.

Similarity of poly(A) and capture transcriptomes from intact RNA. Properties of fragments from both types of libraries. Separate bars (colors) for each replicate in A,C,D. (A) Alignment rates and library strand-specificity (% fragments aligned to the transcribed strand). (B) Types of genomic alignment regions by fraction of assigned fragments and fraction of discovered variants. (C) Efficiency of rRNA depletion (% fragments aligning to ribosomal RNA). (D) Overrepresentation of poly(A) and poly(T) hexamers. (E) Global concordance of detected genes and called variants within all exonic regions. (F) Fraction of assigned reads by biological gene category.

This Article

  1. Genome Res. 25: 1372-1381

Preprint Server