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Neofunctionalization, drift, and genetic conflict appear to have driven a near complete loss of sequence similarity among modern tetherin genes and their sister genes.
The results prove that the extraction of dog hair mitochondrial DNA can easily be automated to provide sufficient DNA yield for the amplification of a forensically useful long mitochondrial DNA fragment or alternatively two short fragments with minimal loss of sequence in case of degraded samples.
Third, groups G1 to G3 are characterized by specific gain or loss of sequence patterns.
In S. anglica allopolyploidy induced few changes in genome structure, but there is epigenetic reprogramming [5], [9], while in Senecio [10], [11] and Tragopogon [12] allopolyploids there are substantial genetic changes including loss of sequence (genomic DNA profiles) and perturbations to the transcriptome (cDNA profiles).
If the loss of sequence data can be afforded, reads with high error rates (for example containing low base quality scores or ambiguous bases) and short reads should be filtered prior to using DeconSeq to ensure high accuracy of the contaminant classifications.
This indicates a duplication of a region containing this structure followed by loss of sequence.
Similar(20)
CNV can be a tandem or inverted duplication or may involve complex gain or loss of sequences at multiple sites within the genome [2].
Loss of sequences at 5q was linked to allele loss at 17p with a single exception.
Sequence analyses reveal single nucleotide changes, loss of sequences and, surprisingly, acquisition of unique genomic insertions.
Loss of sequences from human chromosome 10q has been reported in several different cancers.
The largest loss of sequences occurred at the first filtering step (complexity and size-range) with many of these sequences likely representing partial degradation products of mRNAs.
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