The DOI matches its Crossref record; 7 of the 7 references it cites were found in a registry or an index.
Correction: Initial sequencing and analysis of the human genome
Abstract
Nature 409 , 860 –921 (2001 ) . We have identified several items requiring correction or clarification in our paper on the sequencing of the human genome. • Six additional authors should have been included: Pieter de Jong, Joseph J. Catanese, and Kazutoyo Osoegawa (Department of Cancer Genetics, Roswell Park Cancer Institute, Buffalo, New York 14263, USA; present address: Children's Hospital Oakland Research Institute, 747 52nd street Oakland, California 94609, USA) and Hiroaki Shizuya, Sangdun Choi and Yu-Juin Chen (Division of Biology, California Institute of Technology, Pasadena, California 91125, USA).
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.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Most eukaryotic genomes contain a large number of interspersed repeats that by and large represent copies of transposable elements (TEs) at varying stages of evolutionary decay (Smit 1999;Consortium and International Human Genome Sequencing Consortium 2001;Jurka et al. 2007;Huang et al. 2012;Bourque et al. 2018).”
From RepeatModeler2 for automated genomic discovery of transposable element families (2020) · cites this paper as Consortium and International Human Genome Sequencing Consortium 2001
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
Consed: A Graphical Tool for Sequence Finishing
Gordon, D., Abajian, C., & Green, P. (1998) · Genome Research · doi:10.1101/gr.8.3.195 · Cited by 3,302
Microbial Genes in the Human Genome: Lateral Transfer or Gene Loss?
Salzberg, S. L., White, O., Peterson, J., & Eisen, J. A. (2001) · Science · doi:10.1126/science.1061036 · Cited by 326
Transduction of 3'-flanking sequences is common in L1 retrotransposition
Goodier, J. L. (2000) · Human Molecular Genetics · doi:10.1093/hmg/9.4.653 · Cited by 277
Multiple Isozymes of Heparan Sulfate/Heparin GlcNAcN-Deacetylase/GlcN N-Sulfotransferase
Aikawa, J.-I., Grobe, K., Tsujimoto, M., & Esko, J. D. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m009606200 · Cited by 237
Phylogenetic analyses do not support horizontal gene transfers from bacteria to vertebrates
Stanhope, M. J., Lupas, A. N., Italia, M. J., Koretke, K. K., Volker, C., & Brown, J. R. (2001) · Nature · doi:10.1038/35082058 · Cited by 226
Burgess, D. L., Gefrides, L. A., Foreman, P. J., & Noebels, J. L. (2001) · Genomics · doi:10.1006/geno.2000.6440 · Cited by 110
Roelofs, J., & Haastert, P. J. M. V. (2001) · Nature · doi:10.1038/35082627 · Cited by 80
Research works printed but not linked: 1
- Staden, R., Beal, K. F. & Bonfield, J. K. The Staden package. 1998. Methods Mol. Biol. 132, 115–130 (2000).
Cited by
Finishing the euchromatic sequence of the human genome
International Human Genome Sequencing Consortium (2004) · Nature · doi:10.1038/nature03001 · Cited by 4,971
Self-citationRepeatModeler2 for automated genomic discovery of transposable element families
Flynn, J. M., Hubley, R., Goubert, C., Rosen, J., Clark, A. G., Feschotte, C., & Smit, A. F. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1921046117 · Cited by 3,848
Polycystic Ovary Syndrome: An Evolutionary Adaptation to Lifestyle and the Environment
Parker, J., O’Brien, C., Hawrelak, J., & Gersh, F. L. (2022) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph19031336 · Cited by 114
“The mapping of the human genome in 2003 (84) and the publication of the human haplotype map (more than one million single nucleotide polymorphisms of common genetic variants) in 2005 (85), lead to the realisation that most DNA variation is shared by all humans and is inherited as blocks of linked genes (linkage disequ…”
BackgroundKatori, M., Shi, S., Ode, K. L., Tomita, Y., & Ueda, H. R. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2116729119 · Cited by 75
Metadata
- Authors
- International Human Genome Sequencing Consortium
- Venue
- Nature
- Published
- 2001-08-01
- Volume
- 412
- Issue
- 6846
- Pages
- 565-566
- ISSN
- 0028-0836
- 1476-4687
- PMC
- PMC8127813
- Cited by
- 92
- References
- 7
- Language
- en
- Licence
- creativecommons.org/licenses/by-nc-sa/3.0/ (tdm)
- creativecommons.org/licenses/by-nc-sa/3.0/ (vor)
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: Correction: Initial sequencing and analysis of the human genome. https://app.cochat.ai/papers/10.1038/35087627
- The paper
- International Human Genome Sequencing Consortium. (2001). Correction: Initial sequencing and analysis of the human genome. Nature. https://doi.org/10.1038/35087627
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.
