Downloads provided by UsageCounts
doi: 10.5281/zenodo.50492
The Variant Effect Predictor determines the effect of genomic variants (SNPs, insertions, deletions, CNVs or structural variants) on genes, transcripts, and protein sequence, as well as regulatory regions. This zip file contains v84 of the VEP script with the BioPerl and Ensembl API dependencies included. http://www.ensembl.org/vep
Function analysis, variant, annotation, effect, snp, Genetic variation, Genomics
Function analysis, variant, annotation, effect, snp, Genetic variation, Genomics
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 0 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Average | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Average | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Average |
| views | 37 | |
| downloads | 2 |

Views provided by UsageCounts
Downloads provided by UsageCounts