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The empty capsid structure suggests a mechanism for transcript release from actively transcribing particles.
Until recently probe sets were not designed for transcript specificity.
This allows comparison of QTL controlling metabolite accumulation with eQTL for transcript levels.
Allelic gene structure variations and alternative splicing are responsible for transcript structure variations.
TC stands for transcript cluster ID.
Scripture was used for transcript reconstruction.
ATH1 array was used for transcript profiling.
RNA samples were used for transcript sequencing and SNP calling.
The same technique was used for transcript analyses.
This study used three different criteria for transcript selection.
No PCR product was obtained for transcript T2.
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