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Both libraries were sequenced using the Roche GS FLX + instrument.
Both libraries were sequenced by Illumina at BGI (Beijing, China).
Both libraries were sequenced using the C2 chemistry and C2-XL enzyme.
Both libraries were sequenced with MiSeq Reagent Kit v3 600 cycles (Illumina) on a MiSeq instrument.
A total of 753 clones from both libraries were sequenced and annotated, as summarized in Table 1.
Two separate cDNA libraries of short RNAs were generated from Medicago truncatula leaves and both libraries were sequenced by Solexa (Illumina).
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Both cDNA libraries were sequenced on an Illumina GA IIx sequencer, obtaining 35 bases long single reads from their 5′-ends.
Both parental libraries were sequenced in their own lanes, and hybrid pools 1 and 2 were each sequenced separately.
In total 16,476 ESTs from both cDNA libraries were sequenced, comprising 8,163 and 8,313 ESTs from libraries I and II, respectively.
For amplicon libraries, both 16S rDNA amplicon libraries were sequenced as part of an amplicon pool made from equal amounts of 24 other amplicon libraries.
Libraries were sequenced on both on HiSeq2500 and MiSeq Illumina sequencers Number of total miRNAs expected per million reads at three different thresholds of detection MicroRNA expression patterns can be tissue and cell specific.
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