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. 2016 Apr 14;4:e1828. doi: 10.7717/peerj.1828

Table 5. Comparison of fold change differences of 29 transcripts between EO and muscle measured by qRT-PCR and RNA-seq.

qRT-PCR measurements were normalized against the geometric means of two internal reference genes: rps11, and snrpb. For all qRT-PCR ratios, n = 4. Statistical analysis of the qRT-PCR dataset identified five significantly differentially expressed transcripts (p ≤ 0.05, designated ‘*’). All RNA-seq ratios (n = 1) were considered to be differentially expressed if the difference in transcript expression was more than 4-fold different between EO and muscle. †—To date, we have not resolved the identity of all fast-twitch and slow-twitch myosin heavy chain isoforms transcribed in muscle and EO of S. macrurus and therefore we did not include RNAseq data for myh-f and myh-s in this table.

(A) Sarcomeric structure
hsp70 hsp90a2 plec ank2 dmd cryaba actn2 myoz3 myom1 ckma ttnB myh10 mylk4 myh-f myh-s
qRT-PCR Fold-change 2.37 0.41 2.28 5.89* 1.26 1.03 0.77 0.72 0.35 0.38 0.66 3.88 0.90 0.22 0.02
Standard error 0.16 0.05 0.10 0.34 0.02 0.12 0.14 0.13 0.01 0.02 0.05 0.57 0.07 0.03 0.01
P-value 0.08 0.18 0.10 0.04 0.38 0.99 0.65 0.38 0.08 0.14 0.66 0.08 0.99 0.26 0.09
RNA-seq Fold-change 3.54 0.70 3.61 4.75 2.24 6.46 0.20 1.50 0.62 0.70 0.70 12.19 0.33