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Exact(10)
Our detection rate for alternative transcript variants is expected to fall short of those estimates for two reasons.
However, neither of the two variants is expected to be inert by comparative genomic analysis.
Hence, in an expanding population an excess of low frequency variants is expected for all loci.
The identification of causative genetic variants is expected to be the starting point of RP treatment.
Increased power to detect genetic variants is expected using patients belonging to genetically more homogeneous subgroups, rather than analyzing more heterogeneous groupings.
Each variant-calling pipeline detects variants that others do not, and the accuracy of these discordant variants is expected to be low, but not zero.
Similar(50)
If heterozygosity was the cause of variation, two variants were expected at a nucleotide position in a stack of reads, and the expected frequency of each variant was 0.5.
Because most common alleles in human populations are already captured in dbSNP, novel variants are expected to be rare, and therefore much more likely to be found as heterozygotes.
However, the differences between both variants are expected to be small.
After the exomes of these four cases have been sequenced, many individual variants are expected to be found.
At least three variants are expected to be debuted tonight: one each for T-Mobile, AT&T, and Sprint.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com