The DOI matches its Crossref record; 6 of the 6 references it cites were found in a registry or an index.
Using DECIPHER v2.0 to Analyze Big Biological Sequence Data in R
Open accessAbstract
In recent years, the cost of DNA sequencing has decreased at a rate that has outpaced improvements in memory capacity.It is now common to collect or have access to many gigabytes of biological sequences.This has created an urgent need for approaches that analyze sequences in subsets without requiring all of the sequences to be loaded into memory at one time.It has also opened opportunities to improve the organization and accessibility of information acquired in sequencing projects.The DECIPHER package offers solutions to these problems by assisting in the curation of large sets of biological sequences stored in compressed format inside a database.This approach has many practical advantages over standard bioinformatics workflows, and enables large analyses that would otherwise be prohibitively time consuming.
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
Gapped BLAST and PSI-BLAST: a new generation of protein database search programs
Altschul, S. (1997) · Nucleic Acids Research · doi:10.1093/nar/25.17.3389 · Cited by 73,302
Reducing the Effects of PCR Amplification and Sequencing Artifacts on 16S rRNA-Based Studies
Schloss, P. D., Gevers, D., & Westcott, S. L. (2011) · PLoS ONE · doi:10.1371/journal.pone.0027310 · Cited by 2,112
DECIPHER: harnessing local sequence context to improve protein multiple sequence alignment
Wright, E. S. (2015) · BMC Bioinformatics · doi:10.1186/s12859-015-0749-z · Cited by 385
Self-citationCompression of next-generation sequencing reads aided by highly efficient de novo assembly
Jones, D. C., Ruzzo, W. L., Peng, X., & Katze, M. G. (2012) · Nucleic Acids Research · doi:10.1093/nar/gks754 · Cited by 161
Data compression for sequencing data
Deorowicz, S., & Grabowski, S. (2013) · Algorithms for Molecular Biology · doi:10.1186/1748-7188-8-25 · Cited by 85
Wandelt, S., Bux, M., & Leser, U. (2014) · Current Bioinformatics · doi:10.2174/1574893609666140516010143 · Cited by 56
Cited by
Design and testing of a humanized porcine donor for xenotransplantation
Anand, R. P., Layer, J. V., Heja, D., Hirose, T., Lassiter, G., Firl, D. J., Paragas, V. B., Akkad, A., Chhangawala, S., Colvin, R. B., et al. (2023) · Nature · doi:10.1038/s41586-023-06594-4 · Cited by 302
Microbial composition and functional diversity differ across urban green infrastructure types
Gill, A. S., Purnell, K., Palmer, M. I., Stein, J., & McGuire, K. L. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.00912 · Cited by 64
Lecoeuvre, A., Ménez, B., Cannat, M., Chavagnac, V., & Gérard, E. (2021) · The ISME Journal · doi:10.1038/s41396-020-00816-7 · Cited by 62
Keskitalo, A., Aatsinki, A.-K., Kortesluoma, S., Pelto, J., Korhonen, L., Lahti, L., Lukkarinen, M., Munukka, E., Karlsson, H., & Karlsson, L. (2021) · Stress · doi:10.1080/10253890.2021.1895110 · Cited by 44
Castro-Severyn, J., Pardo-Esté, C., Mendez, K. N., Fortt, J., Marquez, S., Molina, F., Castro-Nallar, E., Remonsellez, F., & Saavedra, C. P. (2021) · Microbiology Spectrum · doi:10.1128/spectrum.00444-21 · Cited by 36
Metadata
- Authors
- Wright, E.
- Venue
- The R Journal
- Publisher
- The R Foundation
- Published
- 2016
- Volume
- 8
- Issue
- 1
- Pages
- 352
- ISSN
- 2073-4859 (ISSN-L)
- OpenAlex
- W2785846143
- Cited by
- 1,016
- References
- 6
- FWCI
- 9.63
- Type
- journal article
- Language
- en
- Open access
- hybrid
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
How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Using DECIPHER v2.0 to Analyze Big Biological Sequence Data in R. https://app.cochat.ai/papers/10.32614/rj-2016-025
- The paper
- Wright, E. (2016). Using DECIPHER v2.0 to Analyze Big Biological Sequence Data in R. The R Journal. https://doi.org/10.32614/rj-2016-025
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.