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Additionally, larval transcription profiles in abalone show that the expression of many transcripts are affected by interactions with exogenous cues such as settlement substrate [62], and in urchins, may be the target of extensive selective pressure [63].
But the transcript capture method has long been viewed as most likely to give a very incomplete picture of the human gene repertoire, because many transcripts are made rarely and in minute quantities by specialized cells.
In fact, only ~10 20% of transcripts are reverse transcribed with current methods and many transcripts are not full-length [9].
Many transcripts are dramatically changed and there is a high level of consistency among the different RNA samples when examining those that are markedly altered (see Text S1).
Interestingly, many transcripts are common among EVs released from different cancer cell types [ 98].
According to Dinger et al., [ 54], many transcripts are categorized as bifunctional RNAs.
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Many transcripts were differentially expressed between embryonic and postnatal OB (unpublished data).
In contrast, many transcripts were repressed at 6 hours, at both of the tested temperatures (Figure 5).
Although many transcripts were encoded unknown function, we still found significant enrichment of GO terms in molecular function including binding, metabolism and transport.
When we compared the "gold standard" to our initial gene build, many transcripts were missing.
Many transcripts were peaking around known optimal fruit stages for flavor production.
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