The phrase "affordable variant" is correct and usable in written English.
It can be used when referring to a less expensive option or version of a product or service.
Example: "The company has released an affordable variant of their flagship smartphone, making it accessible to a wider audience."
Alternatives: "budget-friendly option" or "cost-effective alternative."
Establishment of large collections of DNA samples from lupus patients and controls, along with advances in technology that have made large scale studies of genetic variants more affordable, have led to successful genome-wide association studies (GWAS) supported by government agencies, foundations, industry and academic centers [ 7- 10].
Recently hypothesis free genome wide approaches became affordable and identified novel genetic variants in pathways not being suspected to be involved in the development of these lesions previously.
With the generation and analysis of NGS data becoming more accessible and affordable, a comprehensive catalog of variants for most (if not all) vision-related traits seems a viable prospect.
As Facebook's data scientists explain, "the original variant in support of Affordable Care Act (aka Obamacare) was propagated primarily by liberals, while those mentioning government and taxes slanted conservative.
The main advantage of the candidate SNP approach is that such studies are affordable, as only a limited number of variants are studied and a relatively small sample size can be used.
The concept presents an affordable assistance potential for development of new products variants along the product emergence process (PEP).
Nevertheless, the detection of rare and unique variants via direct sequencing has become more affordable with the advancement of next-generation methods.
In recent years, massively parallel DNA (i.e. next generation) sequencing has become increasingly affordable [ 18], enabling the discovery of causative DNA variants in rare genetic diseases [ 19- 21] and providing new insights into carcinogenesis and autoimmunity [ 22- 32].
Have a glass of sangria — there's a bracingly tart variant made with beer — or one of the many affordable Spanish wines.
The cost of whole genome sequencing (WGS) may soon become affordable and the WGS approach will enable the discovery of both common and rare variants in the genome.
