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Unlike chromosome cores, subtelomeres recombine ectopically, permitting sequence exchange or modification between different chromosomes, introducing diversity.
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While template reads come from DNA strands that are primed by a leader adapter and passed through the pore, the complement reads are generated only if a second adapter (hairpin adapter) is present in the same DNA fragment, thus permitting sequencing both strands of a single molecule in a concatenated manner.
These techniques permit sequence analysis with scoring matrices at speeds that are several times faster than existing programs.
On a database of 12 177 alignment blocks, our techniques permit sequence analysis at a speed of 225 residues/s for a p threshold of 10-6, and 541 residues/s for a p threshold of 10-20.
One such approach is the Smith-Waterman algorithm [ 3], which permits sequence ambiguity, but also provides high accuracy and flexibility, although not with high processing speed.
R-gene evolution is thought to be facilitated by the formation of R-gene clusters, which permit sequence exchanges via recombinatorial mispairing and generate high haplotypic diversity.
In addition, it was not possible to acquire ADC and MRS data on every occasion because of a number of problems including hardware failure and an inability to acquire sufficient signal to permit sequence optimisation.
To address this problem, a multi-objective hybrid control design methodology is developed that employs the corresponding mode-specific controller in each mode, and organizes a rapid and smooth steady-state switching, or transfer, between these controllers to permit sequencing of the operating modes, as necessary.
This began with a rigorous check that the existing consents and/or research ethics approval attached to the samples also permitted sequencing in a project such as UK10K, and the deposition of data in the EGA.
Meanwhile, the QTL study using ddRAD - sequencing permitted sequencing of over 1000 individuals in a single HiSeq 2000 lane [ 13].
For this low stringency search, we used an evalue ≤ 0.01, required at least a 40percentt match between the query sequences and the hit, and permitted sequences with unidentified nucleotides ('N') in their coding and LTR sequences.
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