The DOI matches its Crossref record; 41 of the 41 references it cites were found in a registry or an index.
Genome-wide Single-Cell Analysis of Recombination Activity and De Novo Mutation Rates in Human Sperm
Open accessAbstract
SUMMARY Meiotic recombination and de novo mutation are the two main contributions towards gamete genome diversity, and many questions remain about how an individual human’s genome is edited by these two processes. Here, we describe a high-throughput method for single-cell whole-genome analysis which was used to measure the genomic diversity in one individual’s gamete genomes. A microfluidic system was used for highly parallel sample processing and to minimize non-specific amplification. High-density genotyping results from 91 single cells were used to create a personal recombination map, which was consistent with population-wide data at low resolution but revealed significant differences from pedigree data at higher resolution. We used the data to test for meiotic drive and found evidence for gene conversion. High throughput sequencing on 31 single cells was used to measure the frequency of large-scale genome instability, and deeper sequencing of eight single cells revealed de novo mutation rates with distinct characteristics.
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
A haplotype map of the human genome
The International HapMap Consortium (2005) · Nature · doi:10.1038/nature04226 · Cited by 5,858
Tumour evolution inferred by single-cell sequencing
Navin, N., Kendall, J., Troge, J., Andrews, P., Rodgers, L., McIndoo, J., Cook, K., Stepansky, A., Levy, D., Esposito, D., et al. (2011) · Nature · doi:10.1038/nature09807 · Cited by 2,598
The complete genome of an individual by massively parallel DNA sequencing
Wheeler, D. A., Srinivasan, M., Egholm, M., Shen, Y., Chen, L., McGuire, A., He, W., Chen, Y.-J., Makhijani, V., Roth, G. T., et al. (2008) · Nature · doi:10.1038/nature06884 · Cited by 1,838
The Diploid Genome Sequence of an Individual Human
Levy, S., Sutton, G., Ng, P. C., Feuk, L., Halpern, A. L., Walenz, B. P., Axelrod, N., Huang, J., Kirkness, E. F., Denisov, G., et al. (2007) · PLoS Biology · doi:10.1371/journal.pbio.0050254 · Cited by 1,778
A Fine-Scale Map of Recombination Rates and Hotspots Across the Human Genome
Myers, S., Bottolo, L., Freeman, C., McVean, G., & Donnelly, P. (2005) · Science · doi:10.1126/science.1117196 · Cited by 1,134
PRDM9 Is a Major Determinant of Meiotic Recombination Hotspots in Humans and Mice
Baudat, F., Buard, J., Grey, C., Fledel-Alon, A., Ober, C., Przeworski, M., Coop, G., & de Massy, B. (2010) · Science · doi:10.1126/science.1183439 · Cited by 1,026
The origins, patterns and implications of human spontaneous mutation
Crow, J. F. (2000) · Nature Reviews Genetics · doi:10.1038/35049558 · Cited by 928
Wong, C. C., Loewke, K. E., Bossert, N. L., Behr, B., De Jonge, C. J., Baer, T. M., & Pera, R. A. R. (2010) · Nature Biotechnology · doi:10.1038/nbt.1686 · Cited by 783
Self-citationConception to ongoing pregnancy: the 'black box' of early pregnancy loss
Macklon, N. S. (2002) · Human Reproduction Update · doi:10.1093/humupd/8.4.333 · Cited by 783
Drive Against Hotspot Motifs in Primates Implicates the PRDM9 Gene in Meiotic Recombination
Myers, S., Bowden, R., Tumian, A., Bontrop, R. E., Freeman, C., MacFie, T. S., McVean, G., & Donnelly, P. (2010) · Science · doi:10.1126/science.1182363 · Cited by 683
Clinical assessment incorporating a personal genome
Ashley, E. A., Butte, A. J., Wheeler, M. T., Chen, R., Klein, T. E., Dewey, F. E., Dudley, J. T., Ormond, K. E., Pavlovic, A., Morgan, A. A., et al. (2010) · The Lancet · doi:10.1016/s0140-6736(10)60452-7 · Cited by 674
Self-citationSingle-Cell Exome Sequencing Reveals Single-Nucleotide Mutation Characteristics of a Kidney Tumor
Xu, X., Hou, Y., Yin, X., Bao, L., Tang, A., Song, L., Li, F., Tsang, S., Wu, K., Wu, H., et al. (2012) · Cell · doi:10.1016/j.cell.2012.02.025 · Cited by 667
Self-citationSiva, N. (2008) · Nature Biotechnology · doi:10.1038/nbt0308-256b · Cited by 622
High-resolution mapping of meiotic crossovers and non-crossovers in yeast
Mancera, E., Bourgon, R., Brozzi, A., Huber, W., & Steinmetz, L. M. (2008) · Nature · doi:10.1038/nature07135 · Cited by 613
Fine-scale recombination rate differences between sexes, populations and individuals
Kong, A., Thorleifsson, G., Gudbjartsson, D. F., Masson, G., Sigurdsson, A., Jonasdottir, A., Walters, G. B., Jonasdottir, A., Gylfason, A., Kristinsson, K. T., et al. (2010) · Nature · doi:10.1038/nature09525 · Cited by 582
Variation in genome-wide mutation rates within and between human families
the 1000 Genomes Project (2011) · Nature Genetics · doi:10.1038/ng.862 · Cited by 581
Germ-line mutations of the APC gene in 53 familial adenomatous polyposis patients.
Miyoshi, Y., Ando, H., Nagase, H., Nishisho, I., Horii, A., Miki, Y., Mori, T., Utsunomiya, J., Baba, S., & Petersen, G. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.10.4452 · Cited by 566
Single-Cell Exome Sequencing and Monoclonal Evolution of a JAK2-Negative Myeloproliferative Neoplasm
Hou, Y., Song, L., Zhu, P., Zhang, B., Tao, Y., Xu, X., Li, F., Wu, K., Liang, J., Shao, D., et al. (2012) · Cell · doi:10.1016/j.cell.2012.02.028 · Cited by 541
Self-citationA common sequence motif associated with recombination hot spots and genome instability in humans
Myers, S., Freeman, C., Auton, A., Donnelly, P., & McVean, G. (2008) · Nature Genetics · doi:10.1038/ng.213 · Cited by 447
Single-molecule sequencing of an individual human genome
Pushkarev, D., Neff, N. F., & Quake, S. R. (2009) · Nature Biotechnology · doi:10.1038/nbt.1561 · Cited by 442
Self-citationCoop, G., Wen, X., Ober, C., Pritchard, J. K., & Przeworski, M. (2008) · Science · doi:10.1126/science.1151851 · Cited by 368
Whole-genome molecular haplotyping of single cells
Fan, H. C., Wang, J., Potanina, A., & Quake, S. R. (2011) · Nature Biotechnology · doi:10.1038/nbt.1739 · Cited by 325
Self-citationIntense and highly localized gene conversion activity in human meiotic crossover hot spots
Jeffreys, A. J., & May, C. A. (2004) · Nature Genetics · doi:10.1038/ng1287 · Cited by 295
Nanoliter Reactors Improve Multiple Displacement Amplification of Genomes from Single Cells
Marcy, Y., Ishoey, T., Lasken, R. S., Stockwell, T. B., Walenz, B. P., Halpern, A. L., Beeson, K. Y., Goldberg, S. M. D., & Quake, S. R. (2007) · PLoS Genetics · doi:10.1371/journal.pgen.0030155 · Cited by 286
Self-citationStrong male-driven evolution of DNA sequences in humans and apes
Makova, K. D., & Li, W.-H. (2002) · Nature · doi:10.1038/416624a · Cited by 252
Sequence Variants in the RNF212 Gene Associate with Genome-Wide Recombination Rate
Kong, A., Thorleifsson, G., Stefansson, H., Masson, G., Helgason, A., Gudbjartsson, D. F., Jonsdottir, G. M., Gudjonsson, S. A., Sverrisson, S., Thorlacius, T., et al. (2008) · Science · doi:10.1126/science.1152422 · Cited by 219
Decontamination of MDA Reagents for Single Cell Whole Genome Amplification
Woyke, T., Sczyrba, A., Lee, J., Rinke, C., Tighe, D., Clingenpeel, S., Malmstrom, R., Stepanauskas, R., & Cheng, J.-F. (2011) · PLoS ONE · doi:10.1371/journal.pone.0026161 · Cited by 205
Human recombination hot spots hidden in regions of strong marker association
Jeffreys, A. J., Neumann, R., Panayi, M., Myers, S., & Donnelly, P. (2005) · Nature Genetics · doi:10.1038/ng1565 · Cited by 171
Human Male Recombination Maps for Individual Chromosomes
Sun, F., Oliver‐Bonet, M., Liehr, T., Starke, H., Ko, E. M., RADEMAKER, A. W., Navarro, J., Benet, J., & Martin, R. H. (2004) · The American Journal of Human Genetics · doi:10.1086/382138 · Cited by 132
Twelve new patients with 13q deletion syndrome: Genotype–phenotype analyses in progress
Quēlin, C., Bendavid, C., Dubourg, C., Rochebrochard, C. D. L., Lucas, J., Henry, C., Jaillard, S., Loget, P., Lœuillet, L., Lacombe, D., et al. (2008) · European Journal of Medical Genetics · doi:10.1016/j.ejmg.2008.10.002 · Cited by 130
Digital MDA for enumeration of total nucleic acid contamination
Blainey, P. C., & Quake, S. R. (2010) · Nucleic Acids Research · doi:10.1093/nar/gkq1074 · Cited by 125
Self-citationEvidence for Extensive Transmission Distortion in the Human Genome
Zöllner, S. K., Wen, X., Hanchard, N. A., Herbert, M., Ober, C., & Pritchard, J. K. (2004) · The American Journal of Human Genetics · doi:10.1086/381131 · Cited by 117
Sperm aneuploidy rates in younger and older men
Luetjens, C. M., Rolf, C., Gassner, P., Werny, J. E., & Nieschlag, E. (2002) · Human Reproduction · doi:10.1093/humrep/17.7.1826 · Cited by 116
Determinism and stochasticity during maturation of the zebrafish antibody repertoire
Jiang, N. J., Weinstein, J. A., Penland, L., White, R. A., III, Fisher, D. S., & Quake, S. R. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1014277108 · Cited by 107
Self-citationLi, J., Harris, R. A., Cheung, S. W., Coarfa, C., Jeong, M., Goodell, M. A., White, L. D., Patel, A., Kang, S.-H. L., Shaw, C. A., et al. (2012) · PLoS Genetics · doi:10.1371/journal.pgen.1002692 · Cited by 91
Mismatch repair proteins as sensors of alkylation DNA damage
Wang, J. Y. J., & Edelmann, W. (2006) · Cancer Cell · doi:10.1016/j.ccr.2006.05.013 · Cited by 87
Self-citationPolymorphic Variation in Human Meiotic Recombination
Cheung, V. G., Burdick, J. T., Hirschmann, D., & Morley, M. P. (2007) · The American Journal of Human Genetics · doi:10.1086/512131 · Cited by 85
High-Resolution Recombination Patterns in a Region of Human Chromosome 21 Measured by Sperm Typing
Tiemann‐Boege, I., Calabrese, P. P., Cochran, D. M., Sokol, R. Z., & Arnheim, N. (2006) · PLoS Genetics · doi:10.1371/journal.pgen.0020070 · Cited by 78
Webb, A. J., Berg, I. L., & Jeffreys, A. J. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804933105 · Cited by 73
Estimating Meiotic Gene Conversion Rates From Population Genetic Data
Gay, J., Myers, S., & McVean, G. (2007) · Genetics · doi:10.1534/genetics.107.078907 · Cited by 65
Experimental Generation of SNP Haplotype Signatures in Patients with Sickle Cell Anaemia
Menzel, S., Qin, J., Vasavda, N., Thein, S. L., & Ramakrishnan, R. (2010) · PLoS ONE · doi:10.1371/journal.pone.0013004 · Cited by 10
Cited by
Mapping the Mouse Cell Atlas by Microwell-Seq
Han, X., Wang, R., Zhou, Y., Fei, L., Sun, H., Lai, S., Saadatpour, A., Zhou, Z., Chen, H., Ye, F., et al. (2018) · Cell · doi:10.1016/j.cell.2018.02.001 · Cited by 1,597
The Technology and Biology of Single-Cell RNA Sequencing
Kolodziejczyk, A. A., Kim, J. K., Svensson, V., Marioni, J. C., & Teichmann, S. A. (2015) · Molecular Cell · doi:10.1016/j.molcel.2015.04.005 · Cited by 1,487
Single-cell genome sequencing: current state of the science
Gawad, C., Koh, W., & Quake, S. R. (2016) · Nature Reviews Genetics · doi:10.1038/nrg.2015.16 · Cited by 1,334
Self-citationSingle-cell sequencing-based technologies will revolutionize whole-organism science
Shapiro, E., Biezuner, T., & Linnarsson, S. (2013) · Nature Reviews Genetics · doi:10.1038/nrg3542 · Cited by 1,177
Genome-Wide Detection of Single-Nucleotide and Copy-Number Variations of a Single Human Cell
Zong, C., Lu, S., Chapman, A. R., & Xie, X. S. (2012) · Science · doi:10.1126/science.1229164 · Cited by 1,154
Metadata
- Authors
- Wang, J., Fan, H. C., Behr, B., & Quake, S. R.
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 2012-07
- Volume
- 150
- Issue
- 2
- Pages
- 402-412
- ISSN
- 0092-8674 (ISSN-L)
- OpenAlex
- W1997666780
- Cited by
- 511
- References
- 41
- FWCI
- 57.55
- Type
- journal article
- Language
- en
- Open access
- bronze
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
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.