| The NHGRI GWAS Catalog, a curated resource of SNP-trait associations | 2013/12/06 | English | 1,904 |
| Human Splicing Finder: an online bioinformatics tool to predict splicing signals | 2009/04/01 | English | 1,882 |
| CADD: predicting the deleteriousness of variants throughout the human genome | 2018/10/29 | English | 1,876 |
| The SWISS-PROT protein sequence database and its supplement TrEMBL in 2000 | 2000/01/01 | | 1,876 |
| ConSurf 2016: an improved methodology to estimate and visualize evolutionary conservation in macromolecules | 2016/05/10 | English | 1,876 |
| ARAGORN, a program to detect tRNA genes and tmRNA genes in nucleotide sequences | 2004/01/02 | English | 1,861 |
| tRNAscan-SE On-line: integrating search and context for analysis of transfer RNA genes | 2016/05/12 | English | 1,859 |
| Ensembl 2018 | 2017/11/16 | English | 1,859 |
| agriGO: a GO analysis toolkit for the agricultural community | 2010/04/30 | English | 1,824 |
| CDD/SPARCLE: functional classification of proteins via subfamily domain architectures | 2016/11/29 | English | 1,815 |
| A general method for isolation of high molecular weight DNA from eukaryotes | 1976/09/01 | English | 1,813 |
| Genomics of Drug Sensitivity in Cancer (GDSC): a resource for therapeutic biomarker discovery in cancer cells | 2012/11/22 | English | 1,809 |
| GeSeq – versatile and accurate annotation of organelle genomes | 2017/05/09 | English | 1,800 |
| PANTHER version 14: more genomes, a new PANTHER GO-slim and improvements in enrichment analysis tools | 2018/11/08 | English | 1,779 |
| The Subread aligner: fast, accurate and scalable read mapping by seed-and-vote | 2013/04/03 | English | 1,779 |
| The UNITE database for molecular identification of fungi: handling dark taxa and parallel taxonomic classifications | 2018/10/29 | English | 1,763 |
| STRING 8--a global view on proteins and their functional interactions in 630 organisms | 2009/01/01 | English | 1,754 |
| Improved microbial gene identification with GLIMMER | 1999/12/01 | | 1,741 |
| MEME: discovering and analyzing DNA and protein sequence motifs | 2006/07/01 | English | 1,741 |
| deepTools: a flexible platform for exploring deep-sequencing data | 2014/05/05 | English | 1,736 |
| The Gene Ontology resource: enriching a GOld mine | 2020/12/08 | English | 1,729 |
| HaploReg: a resource for exploring chromatin states, conservation, and regulatory motif alterations within sets of genetically linked variants | 2011/11/07 | English | 1,717 |
| WebGestalt 2019: gene set analysis toolkit with revamped UIs and APIs | 2019/05/22 | English | 1,712 |
| COSMIC: exploring the world's knowledge of somatic mutations in human cancer | 2014/10/29 | English | 1,703 |
| VISTA: computational tools for comparative genomics | 2004/07/01 | English | 1,702 |
| Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification | 2002/06/15 | | 1,698 |
| ClinVar: public archive of relationships among sequence variation and human phenotype | 2013/11/14 | English | 1,696 |
| DrugBank: a knowledgebase for drugs, drug actions and drug targets | 2007/11/29 | English | 1,685 |
| The Reactome Pathway Knowledgebase | 2017/11/14 | English | 1,676 |
| ClinVar: public archive of interpretations of clinically relevant variants | 2015/11/17 | English | 1,667 |