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An introduction to the predictors of pathogenic point mutations

Single nucleotide variation is a change in a single nucleotide in a sequence irrespective of the frequency of the variation. Single nucleotide variants (SNVs) play a very important role in causing several diseases such as the tumor, cancer, etc. Many efforts have been made to identify the SNVs which were initially based on identifying non-synonymous mutations in coding regions of the genomes. Continue reading “An introduction to the predictors of pathogenic point mutations” »

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BiR: Impact report – July 2016 & More

As we improve the quality of articles and as we are nearing our first collective birthday, Bioinformatics Review has expanded its reach, opening new avenues. The progress is summarised as below: We have partnered with London Business Conference Group to be official media partner for Discovery Informatics and Analytics Summit 2016 Our scientific articles are starting… Keep Reading

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