Google Scholar Mentions

This tracks the cumulative number of mentions of the keywords anvil nhgri on Google Scholar. For example, for 2026 only, we’d see the number of hits with the following url: https://scholar.google.com/scholar?hl=en&as_sdt=0%2C21&as_ylo=2026&q=anvil+nhgri&btnG=

This data is fairly small and static, and is thus stored in the data/ directory.

Preview

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…    10

Data information

Column information:

  • original_paper shows papers that we have captured citation information about
  • cite_titles shows papers that cite the original paper
  • linkscolumn 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