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While Simple Sequence Repeats (SSRs) are extremely useful genetic markers, recent advances in technology have produced a shift toward use of single nucleotide polymorphisms (SNPs).
Originally designed as a prototype to support forensic use of single nucleotide polymorphisms (SNPs), FROG-kb provides a freely accessible web interface that facilitates forensic practice and can be useful for teaching and research.
One of the promising methods for analysis of the human genome and identification of genes and genomic regions contributing to phenotypes is the use of single nucleotide polymorphisms (SNPs).
This suggests the use of single nucleotide polymorphism array data is not necessarily a significant bias.
Recent progress in technology for plant genomics has led to the escalation in use of single nucleotide polymorphism (SNP) markers in DNA fingerprinting.
The analytical methods used to process the 15 generated RNA-Seq datasets require the use of single nucleotide activities instead of read mappings.
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The oligonucleotide occurrence was calculated using shift of single nucleotide window.
Although full genome sequence data are typically not available for nonmodel species, evaluations of adaptive variation have recently been addressed using analyses of single nucleotide polymorphism (SNP) loci (Willing et al. 2010; Matala et al. 2011; Hohenlohe et al. 2010).
Genomewide linkage studies are tending toward the use of single-nucleotide polymorphisms (SNPs) as the markers of choice.
The relatively high cost and limited marker density of these methods led to the use of single-nucleotide polymorphisms (SNPs) as the current preferred genotyping system.
The use of single-nucleotide polymorphisms (SNPs) as markers of genetic variation for phylogenetic analysis has been described in many studies [ 23– 28].
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