Drug resistance mutations in HIV: new bioinformatics approaches and challenges
Current Opinion in Virology, ISSN: 1879-6257, Vol: 51, Page: 56-64
2021
- 32Citations
- 147Captures
Metric Options: CountsSelecting the 1-year or 3-year option will change the metrics count to percentiles, illustrating how an article or review compares to other articles or reviews within the selected time period in the same journal. Selecting the 1-year option compares the metrics against other articles/reviews that were also published in the same calendar year. Selecting the 3-year option compares the metrics against other articles/reviews that were also published in the same calendar year plus the two years prior.
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations32
- Citation Indexes32
- 32
- CrossRef21
- Captures147
- Readers147
- 147
Review Description
Drug resistance mutations appear in HIV under treatment pressure. Resistant variants can be transmitted to treatment-naive individuals, which can lead to rapid virological failure and can limit treatment options. Consequently, quantifying the prevalence, emergence and transmission of drug resistance is critical to effectively treating patients and to shape health policies. We review recent bioinformatics developments and in particular describe: (1) the machine learning approaches intended to predict and explain the level of resistance of HIV variants from their sequence data; (2) the phylogenetic methods used to survey the emergence and dynamics of resistant HIV transmission clusters; (3) the impact of deep sequencing in studying within-host and between-host genetic diversity of HIV variants, notably regarding minority resistant variants.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S1879625721001073; http://dx.doi.org/10.1016/j.coviro.2021.09.009; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85120160775&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/34597873; https://linkinghub.elsevier.com/retrieve/pii/S1879625721001073; https://dx.doi.org/10.1016/j.coviro.2021.09.009
Elsevier BV
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