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NGS has several diagnostic advantages in heterogeneous diseases; that is, all known genes can be effectively sequenced and interpreted simultaneously.
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How these two processes are interlinked, how to design and implement interventions that contribute to the two processes, and how they are effectively sequenced remain a major research gap.
This algorithm is correct since the sequences found are effectively sequences of steps which produce the desired final marking.
Previously published reports [ 11, 39] have shown that mRNAs are also found in isolated exosome fractions and may be effectively quantitated through sequencing.
By utilizing the FSVQ, the inter-frame dependencies within source sequence can be effectively exploited and no side information needs to be transmitted.
Consistent with these publications, our results also indicated that relatively short reads from Illumina paired-end sequencing can be effectively assembled and used for novel gene discovery and SSR marker development in non-model organism.
Consistent with these reports, the results from this research also suggested that short reads from Illumina sequencing can be effectively assembled and used for gene identification and SSR marker development in non-model organisms.
The results showed that signals for 19 out of 20 tested genes were detected, demonstrating the high quality of the assembled results, and also indicating that relatively short reads from Illumina sequencing can be effectively assembled and used for novel gene discovery.
As with other recent studies [ 5, 7, 15, 16], our results indicate that short reads from 454 sequencing runs can be effectively assembled and used to readily characterize the gene space of non-model organisms.
It is important to be aware of the sequence versatility of fulvestrant so that it may be effectively and appropriately incorporated into the endocrine sequence cascade.
We demonstrate herein that this can be effectively accomplished using sequence-specific DNAzymes [ 39- 43].
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