The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
DrivR-Base: A Feature Extraction Toolkit For Variant Effect Prediction Model Construction
Open accessPreprint — published as 10.1093/bioinformatics/btae197
Abstract
Motivation: Recent advancements in sequencing technologies have led to the discovery of numerous variants in the human genome. However, understanding their precise roles in diseases remains challenging due to their complex functional mechanisms. Various methodologies have emerged to predict the pathogenic significance of these genetic variants. Typically, these methods employ an integrative approach, leveraging diverse data sources that provide critical insights into genomic function. Despite the abundance of publicly available data sources and databases, the process of navigating, extracting, and pre-processing features for machine learning models can be daunting. Furthermore, researchers often invest substantial effort in feature extraction, only to later discover that these features lack informativeness. Results: In this paper, we present DrivR-Base , an innovative resource that efficiently extracts and integrates molecular information (features) for single nucleotide variants from a wide range of databases and tools, including AlphaFold, ENCODE, and Variant Effect Predictor . The resulting features can be used as input for machine learning models designed to predict the pathogenic impact of human genome variants in disease. Moreover, these feature sets have applications beyond this, including haploinsufficiency prediction and the development of drug repurposing tools. We describe the resource’s development, practical applications, and potential for future expansion and enhancement. Availability and Implementation: DrivR-Base source code is available at https://github.com/amyfrancis97/DrivR-Base .
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Highly accurate protein structure prediction with AlphaFold
Jumper, J., Evans, R., Pritzel, A., Green, T., Figurnov, M., Ronneberger, O., Tunyasuvunakool, K., Bates, R., Žídek, A., Potapenko, A., et al. (2021) · Nature · doi:10.1038/s41586-021-03819-2 · Cited by 43,764
Research works printed but not linked: 32
- Adzhubei, I. , Jordan, D. M. , and Sunyaev, S. R. (2013). Predicting functional effect of human missense mutations using polyphen-2. Current protocols in human genetics / editorial board, Jonathan L. Haines … [et al.], 0 7:Unit7.20. · DOI · Paper page
- 10.1093/nar/28.1.235 · DOI · Paper page
- 2022, Variant pathogenic prediction by locus variability: the importance of the current picture of evolution, European Journal of Human Genetics, 30, 555, 10.1038/s41431-021-01034-1 · DOI
- Campbell, C. and Ying, Y. (2011). Learning with Support Vector Machines. Morgan Clay-pool Publishers. · DOI
- Cheng, J. , Novati, G. , Pan, J. , Bycroft, C. , Žemgulytė, A. , Applebaum, T. , Pritzel, A. , Wong, L. H. , Zielinski, M. , Sargeant, T. , Schneider, R. G. , Senior, A. W. , Jumper, J. , Hassabis, D. , Kohli, P. , and Žiga Avsec (2023). Accurate proteome-wide missense variant effect prediction with alphamissense. Science, 381. · DOI · Paper page
- 10.1093/bioinformatics/btv735 · DOI
- 10.1093/nar/gkx915 · DOI
- 10.1038/nature11247 · DOI · Paper page
- Frazer, J. , Notin, P. , Dias, M. , Gomez, A. , Min, J. K. , Brock, K. , Gal, Y. , and Marks, D. S. (2021). Disease variant prediction with deep generative models of evolutionary data. Nature 2021 599:7883, 599:91–95. · DOI · Paper page
- 10.1093/nar/gkn597 · DOI
- 1992, Exhaustive matching of the entire protein sequence database, Science (New York, N.Y, 256, 1443, 10.1126/science.1604319 · DOI
- 10.1073/pnas.89.22.10915 · DOI · Paper page
- 2022, The use of genomic variants to drive drug repurposing for chronic hepatitis b, Biochemistry and Biophysics Reports, 31, 101307, 10.1016/j.bbrep.2022.101307 · DOI
- 1992, The rapid generation of mutation data matrices from protein sequences, Computer applications in the biosciences : CABIOS, 8, 275
- 10.1016/0014-5793(94)80429-X · DOI
- 10.1093/nar/gkg922 · DOI
- 10.1093/nar/gkx951 · DOI
- 10.1101/gr.229102. Article published online before print in May 2002 · DOI · Paper page
- 10.1186/s13059-015-0866-z · DOI · Paper page
- 10.1093/bioinformatics/16.9.760 · DOI
- 10.1186/1471-2105-13-1 · DOI
- Pollard, K. S. , Hubisz, M. J. , Rosenbloom, K. R. , and Siepel, A. (2009). Detection of non-neutral substitution rates on mammalian phylogenies. Genome Research, 20:gr.097857.109. · DOI · Paper page
- 10.1093/bioinformatics/btu703 · DOI
- 10.1093/nar/gky1016 · DOI · Paper page
- 2017, Cscape: a tool for predicting oncogenic single-point mutations in the cancer genome, Scientific Reports 2017 7:1, 7, 1
- 10.1038/nature08473 · DOI · Paper page
- 10.1016/j.cell.2018.09.045 · DOI · Paper page
- 10.1093/bioinformatics/btv009 · DOI
- 10.1101/gr.3715005 · DOI · Paper page
- Sun, H. and Yu, G. (2019). New insights into the pathogenicity of non-synonymous variants through multi-level analysis. Scientific Reports, 9. · DOI
- 10.1093/nar/gkg296 · DOI
- Woodruff, D. S. (2001). Populations, species, and conservation genetics. Encyclopedia of Biodiversity, page 811. · DOI
Metadata
- Authors
- Francis, A., Campbell, C., & Gaunt, T.
- Affiliations
- University of Bristol (GB)
- Corresponding author
- Francis, Amy
- Venue
- Bioinformatics
- Publisher
- openRxiv
- Published
- 2024-01-17
- Volume
- 40
- Issue
- 4
- ISSN
- 1367-4803 (ISSN-L)
- PMC
- PMC11057939
- OpenAlex
- W4394711091
- Cited by
- 1
- References
- 1
- Citations by year
- 2026: 1
- FWCI
- 0.26
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- cc-by
- Locations
- Bioinformatics (publishedVersion, cc-by)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Funders
- Cancer Research UK (C18281/, C18281/A30905)
- University of Bristol (MC_UU_00032/03)
- Medical Research Council (MC_UU_00032/3, MC_UU_00032/03)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genomics and Rare Diseases
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
- Keywords
- feature extraction, single nucleotide variants, variant effect prediction, pathogenicity prediction, AlphaFold protein structure, variant effect predictors, drug repurposing, Docker containers, reproducibility
- MeSH terms
- Machine Learning, Humans, Software, Genetic Variation, Genome, Human, Computational Biology, Polymorphism, Single Nucleotide, Genomics, Databases, Genetic
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review