Currently this is capped at reporting 10 citations per paper. But this will be fixed soon.
Here we show how to get the total counts per original paper:
library(dplyr)
# here we remove duplicates if there are any of the same titles of citing papers for each original paper and then get a count of the number of rows for each original paper (aka how many times it is cited)
citations %>%
distinct(original_paper, cite_titles, .keep_all = TRUE) %>%
count(original_paper)## # A tibble: 1 × 2
## original_paper n
## <chr> <int>
## 1 Inverting the model of genomics data sharing with the NHGRI Genomic Dat… 10Column information:
original_paper shows papers that we have captured
citation information aboutcite_titles shows papers that cite the original
paperlinkscolumn shows the link for the paper that cites the
original paper (the cite_titles papers).knitr::kable(citations)| original_paper | cite_titles | links |
|---|---|---|
| Inverting the model of genomics data sharing with the NHGRI Genomic Data Science Analysis,… | Deciphering the impact of genomic variation on function | https://www.nature.com/articles/s41586-024-07510-0 |
| Inverting the model of genomics data sharing with the NHGRI Genomic Data Science Analysis,… | The Human Pangenome Project: a global resource to map genomic diversity | https://www.nature.com/articles/s41586-022-04601-8 |
| Inverting the model of genomics data sharing with the NHGRI Genomic Data Science Analysis,… | The Galaxy platform for accessible, reproducible, and collaborative data analyses: 2024 update | https://academic.oup.com/nar/article-abstract/52/W1/W83/7676834 |
| Inverting the model of genomics data sharing with the NHGRI Genomic Data Science Analysis,… | [HTML][HTML] A draft human pangenome reference | https://www.nature.com/articles/s41586-023-05896-x |
| Inverting the model of genomics data sharing with the NHGRI Genomic Data Science Analysis,… | The complete sequence of a human Y chromosome | https://www.nature.com/articles/s41586-023-06457-y |
| Inverting the model of genomics data sharing with the NHGRI Genomic Data Science Analysis,… | The Galaxy platform for accessible, reproducible and collaborative biomedical analyses: 2022 update | https://academic.oup.com/nar/article-abstract/50/W1/W345/6572001 |
| Inverting the model of genomics data sharing with the NHGRI Genomic Data Science Analysis,… | The Galaxy platform for accessible, reproducible and collaborative biomedical analyses: 2018 update | https://academic.oup.com/nar/article-abstract/46/W1/W537/5001157 |
| Inverting the model of genomics data sharing with the NHGRI Genomic Data Science Analysis,… | A complete reference genome improves analysis of human genetic variation | https://www.science.org/doi/abs/10.1126/science.abl3533 |
| Inverting the model of genomics data sharing with the NHGRI Genomic Data Science Analysis,… | [HTML][HTML] Current trends, limitations and future research in the fungi? | https://link.springer.com/article/10.1007/s13225-023-00532-5 |
| Inverting the model of genomics data sharing with the NHGRI Genomic Data Science Analysis,… | Scalable Nanopore sequencing of human genomes provides a comprehensive view of haplotype-resolved variation and methylation | https://www.nature.com/articles/s41592-023-01993-x |