The Diploid Genome Sequence of an Individual Human

Levy, Samuel, Sutton, Granger, Ng, Pauline C, Feuk, Lars, Halpern, Aaron L, Walenz, Brian P, Axelrod, Nelson, Huang, Jiaqi +23 more·2007·PLoS Biology

Cited by (1,000)

Items 501–600 of 1,000

  1. Accurate Distinction of Pathogenic from Benign CNVs in Mental Retardation
    Jayne Y. Hehir‐Kwa, Nienke Wieskamp, Caleb Webber, Rolph Pfundt, Han G. Brunner, Christian Gilissen, Bert B A De Vries, Chris P. Ponting, Joris A. Veltman · 2010 · PLoS Computational Biology
  2. Ethical Endgames: Broad Consent for Narrow Interests; Open Consent for Closed Minds
    Jan Reinert Karlsen, Jan Helge Solbakk, Søren Holm · 2011 · Cambridge Quarterly of Healthcare Ethics
  3. IntSIM: An Integrated Simulator of Next-Generation Sequencing Data
    Xiguo Yuan, Junying Zhang, Liying Yang · 2016 · IEEE Transactions on Biomedical Engineering
  4. CENPT bridges adjacent CENPA nucleosomes on young human α-satellite dimers
    Jitendra Thakur, Steven Henikoff · 2016 · Genome Research
  5. Application of next generation sequencing to molecular diagnosis of inherited diseases.
    Wei Zhang, H. Cui, L. Wong · 2014 · Topics in current chemistry
  6. Restriction Fragment Length Polymorphism Analysis of PCR-Amplified Fragments (PCR-RFLP) and Gel Electrophoresis - Valuable Tool for Genotyping and Genetic Fingerprinting
    Henrik Berg · 2012 · InTech eBooks
  7. Microsatellite Instability in Pediatric High Grade Glioma Is Associated with Genomic Profile and Differential Target Gene Inactivation
    Marta Viana‐Pereira, Alicia Lee, Sergey Popov, Dorine A. Bax, Safa Al‐Sarraj, Leslie Bridges, João Noberto Stávale, Darren R. Hargrave, Chris Jones, Rui Manuel Reis · 2011 · PLoS ONE
  8. The human genome: a multifractal analysis
    Pedro A. Moreno, Patricia E. Vélez, Émber Ubéimar Martínez Flor, Luis E Garreta, Néstor Díaz, Siler Amador, Irene Tischer, José Manuel Gutiérrez, Ashwinikumar K. Naik, Fabián Tobar-Tosse et al. · 2011 · BMC Genomics
  9. Data structures and compression algorithms for high-throughput sequencing technologies
    Kenneth Daily, Paul Rigor, Scott Christley, Xiaohui S. Xie, Pierre Baldi · 2010 · BMC Bioinformatics
  10. Sequencing and analysis of an Irish human genome
    Pin Tong, James G. D. Prendergast, Amanda J. Lohan, Susan Mary Farrington, Simon Cronin, Nial Friel, Daniel G. Bradley, Orla M. Hardiman, A.C.O. Evans, James F. Wilson et al. · 2010 · Genome biology
  11. High-throughput molecular analysis in lung cancer: insights into biology and potential clinical applications
    Sebahat Ocak, Martin L. Sos, Roman Kurt Thomas, Pierre P. Massion · 2009 · European Respiratory Journal
  12. Novel multi-nucleotide polymorphisms in the human genome characterized by whole genome and exome sequencing
    Jeffrey Rosenfeld, Anil K. Malhotra, Todd Lencz · 2010 · Nucleic Acids Research
  13. Different Facets of Copy Number Changes: Permanent, Transient, and Adaptive
    Sweta Mishra, Johnathan R. Whetstine · 2016 · Molecular and Cellular Biology
  14. Evaluation of hybrid and non-hybrid methods for de novo assembly of nanopore reads
    Ivan Sović, Krešimir Križanović, Karolj Skala, Mile Šikić · 2016 · Bioinformatics
  15. A classical revival: Human satellite DNAs enter the genomics era
    Nicolas Altemose · 2022 · Seminars in Cell and Developmental Biology
  16. Investigation and Functional Characterization of Rare Genetic Variants in the Adipose Triglyceride Lipase in a Large Healthy Working Population
    Stefan Coassin, Martina Schweiger, Anita Kloss‐Brandstätter, Claudia Lamina, Margot Haun, Gertraud Erhart, Bernhard Paulweber, Yusof Rahman, Simon Edward Olpin, Heimo Wolinski et al. · 2010 · PLoS Genetics
  17. Mechanisms of Formation of Structural Variation in a Fully Sequenced Human Genome
    Andy Wing Chun Pang, Ohsuke Migita, Jeffrey R. MacDonald, Lars Feuk, Stephen W. Scherer · 2012 · Human Mutation
  18. Alpha-CENTAURI: assessing novel centromeric repeat sequence variation with long read sequencing
    Volkan Sevi̇m, Ali Bashir, Chen-Shan Chin, Karen H. Miga · 2016 · Bioinformatics
  19. Advances of genotyping-by-sequencing in fisheries and aquaculture
    Yanhe Li, Han‐Ping Wang · 2017 · Reviews in Fish Biology and Fisheries
  20. Large vs small genomes in Passiflora: the influence of the mobilome and the satellitome
    Mariela Sader, Magdalena Vaio, Luiz Augusto Cauz‐Santos, Marcelo Carnier Dornelas, Maria Lúcia Carneiro Vieira, Natoniel Franklin de Melo, Andrea Pedrosa‐Harand · 2021 · Planta
  21. Human genomic disease variants: A neutral evolutionary explanation
    Joel T. Dudley, Yuseob Kim, Li Liu, Glenn J. Markov, Kristyn Gerold, Rong Chen, Atul Janardhan Butte, Sudhir Kumar · 2012 · Genome Research
  22. The Road from Next-Generation Sequencing to Personalized Medicine
    Manuel L. Gonzalez‐Garay · 2014 · Personalized Medicine
  23. The promise and reality of personal genomics
    Bryndís Yngvadóttir, Daniel G. MacArthur, Han‐Jun Jin, Chris Tyler‐Smith · 2009 · Genome biology
  24. Genetic determinants of phenotypic diversity in humans
    Nazli G Rahim, Olivier Harismendy, Eric J. Topol, Kelly A. Frazer · 2008 · Genome biology
  25. Comprehensive characterization of horse genome variation by whole‐genome sequencing of 88 horses
    Vidhya Jagannathan, Vinzenz Gerber, Stefan Rieder, Jens Tetens, Georg Erwin Thaller, Cord Drögemüller, Tosso Leeb · 2018 · Animal Genetics
  26. Construction of Human Antibody Gene Libraries and Selection of Antibodies by Phage Display
    André Frenzel, Jonas Kügler, Sonja Wilke, Thomas Schirrmann, Michael Hust · 2013 · Methods in molecular biology
  27. Induced pluripotent stem cells: A new tool to confront the challenge of neuropsychiatric disorders
    Flora Maria Vaccarino, Hanna Elizabeth Stevens, Arif Murat Kocabas, Dean Palejev, Anna M. Szekely, Elena L. Grigorenko, Sherman M. Weissman · 2011 · Neuropharmacology
  28. An Efficient Fluorescence Resonance Energy Transfer (FRET) between Pyrene and Perylene Assembled in a DNA Duplex and Its Potential for Discriminating Single‐Base Changes
    Hiromu Kashida, Tomohiko Takatsu, Koji Sekiguchi, Hiroyuki Asanuma · 2010 · Chemistry - A European Journal
  29. Planning the Human Variome Project: The Spain report
    Jim Kaput, Richard G.H. Cotton, Lauren Hardman, Michael S. Watson, Aida I. Al Aqeel, Jumana Yousuf Al-Aama, Fahd Al‐Mulla, Santos Alonso, Stefan Aretz, Arleen D. Auerbach et al. · 2009 · Human Mutation
  30. The impact of network biology in pharmacology and toxicology
    Gianni Panagiotou, Olivier Taboureau · 2012 · SAR and QSAR in environmental research
  31. Replication of alpha-satellite DNA arrays in endogenous human centromeric regions and in human artificial chromosome
    Indri Erliandri, Haiqing Fu, Megumi Nakano, Jung-Hyun Kim, Karen H. Miga, Mikhail A. Liskovykh, William C. Earnshaw, Hiroshi Masumoto, Natalay Kouprina, Mirit I. Aladjem et al. · 2014 · Nucleic Acids Research
  32. SNPs in MicroRNA Binding Sites as Prognostic and Predictive Cancer Biomarkers
    Carina Preskill, Joanne Barnes Weidhaas · 2013 · Critical Reviews™ in Oncogenesis
  33. Identification of indels in next-generation sequencing data
    Aakrosh Ratan, Thomas L. Olson, Thomas P. Loughran, Webb Miller · 2015 · BMC Bioinformatics
  34. Types of DNA methylation status of the interspersed repetitive sequences for LINE-1, Alu, HERV-E and HERV-K in the neutrophils from systemic lupus erythematosus patients and healthy controls
    Patadon Sukapan, Paramate Promnarate, Yingyos Avihingsanon, Apiwat Mutirangura, Nattiya Hirankarn · 2014 · Journal of Human Genetics
  35. No Evidence of Increased Mutation Rates at Microsatellite Loci in Offspring of A-Bomb Survivors
    Mieko Kodaira, Haruko Ryo, N Kamada, Kyoji Furukawa, N. Takahashi, Hideaki Nakajima, Taisei Nomura, Nori Nakamura · 2010 · Radiation Research
  36. Mutation Rate Distribution Inferred from Coincident SNPs and Coincident Substitutions
    Philip L. F. Johnson, Ines Hellmann · 2011 · Genome Biology and Evolution
  37. Nine things to remember about human genome diversity
    Guido Barbujani, Silvia Ghirotto, Francesca Tassi · 2013 · Tissue Antigens
  38. A time-invariant principle of genome evolution
    Subhajyoti De, M. Madan Babu · 2010 · Proceedings of the National Academy of Sciences
  39. DNA methylation of human endogenous retrovirus in systemic lupus erythematosus
    Jeerawat Nakkuntod, Pattadon Sukkapan, Yingyos Avihingsanon, Apiwat Mutirangura, Nattiya Hirankarn · 2013 · Journal of Human Genetics
  40. Personalized genomic disease risk of volunteers
    Manuel L. Gonzalez‐Garay, Amy L. McGuire, Stacey Pereira, C. Thomas Caskey · 2013 · Proceedings of the National Academy of Sciences
  41. Genome at Juncture of Early Human Migration: A Systematic Analysis of Two Whole Genomes and Thirteen Exomes from Kuwaiti Population Subgroup of Inferred Saudi Arabian Tribe Ancestry
    Osama A Alsmadi, Sumi Elsa John, Gaurav Thareja, Prashantha Hebbar, Dinu Antony, Kazem Behbehani, Thangavel Alphonse Thanaraj · 2014 · PLoS ONE
  42. Increased de novo copy number variants in the offspring of older males
    Traute Flatscher‐Bader, Claire J. Foldi, Suyinn Chong, E. Whitelaw, R J Moser, Thomas H.J. Burne, Darryl Walter Eyles, John Joseph McGrath · 2011 · Translational Psychiatry
  43. Transcriptional analysis of endocrine disruption using zebrafish and massively parallel sequencing
    Michael E. Baker, Gary Hardiman · 2014 · Journal of Molecular Endocrinology
  44. Haplotype phasing of whole human genomes using bead-based barcode partitioning in a single tube
    Fan Zhang, Lena Christiansen, Jerushah Thomas, Dmitry Pokholok, Ros Jackson, Natalie Morrell, Yannan Zhao, Melissa M. Wiley, Emily Welch, Erich B. Jaeger et al. · 2017 · Nature Biotechnology
  45. Description and pilot results from a novel method for evaluating return of incidental findings from next-generation sequencing technologies
    Katrina A.B. Goddard, Evelyn P. Whitlock, Jonathan S. Berg, Marc S. Williams, Elizabeth M. Webber, Jennifer Webster, Jennifer S Lin, Kasmintan A. Schrader, Doug E Campos-Outcalt, Kenneth Offit et al. · 2013 · Genetics in Medicine
  46. Structural and Functional Restraints on the Occurrence of Single Amino Acid Variations in Human Proteins
    Sungsam Gong, Tom L. Blundell · 2010 · PLoS ONE
  47. Theory and Algorithms for the Haplotype Assembly Problem
    Russell S. Schwartz · 2010 · Communications in Information and Systems
  48. MATE-CLEVER: Mendelian-inheritance-aware discovery and genotyping of midsize and long indels
    Tobias Marschall, Iman Hajirasouliha, Alexander Schönhuth · 2013 · Bioinformatics
  49. Next-generation sequencing to identify genetic causes of cardiomyopathies
    N. Norton, Duanxiang Li, R. Hershberger · 2012 · Current Opinion in Cardiology
  50. An evolutionary perspective on Y‐chromosomal variation and male infertility
    Chris Tyler‐Smith · 2008 · International Journal of Andrology
  51. James Watson's genome sequenced at high speed
    Meredith Wadman · 2008 · Nature
  52. Molecular and clinical analyses of 16q24.1 duplications involving FOXF1 identify an evolutionarily unstable large minisatellite
    Avinash V. Dharmadhikari, Tomasz Gambin, Przemysław Szafrański, Wenjian Cao, Frank J. Probst, Weihong Jin, Ping Fang, Krzysztof Gogolewski, Anna Gambin, Jaya K. George‐Abraham et al. · 2014 · BMC Medical Genetics
  53. Genome-wide deserts for copy number variation in vertebrates
    Takashi T Makino, Aoife McLysaght, Masakado Kawata · 2013 · Nature Communications
  54. Mapping the human protein interactome
    Daniel Figeys · 2008 · Cell Research
  55. Lymphoid tissue inducer cells: bridges between the ancient innate and the modern adaptive immune systems
    Peter J. L. Lane, Fiona M. McConnell, David R. Withers, Fabrina Gaspal, Manoj Kumar Saini, Graham Anderson · 2009 · Mucosal Immunology
  56. Using mobile sequencers in an academic classroom
    Sophie Zaaijer, Yaniv Erlich · 2016 · eLife
  57. The History of DNA Sequencing / ISTORIJAT SEKVENCIRANJA DNK
    Miodrag Gužvić · 2013 · Journal of Medical Biochemistry
  58. Genome-wide copy number variations in Oryza sativa L.
    Ping Yu, Caihong Wang, Qun Jie Xu, Yue Feng, Xiaoping Yuan, Hanyong Yu, Yi-Ping Wang, Sheng-Xiang Tang, Xinghua Wei · 2013 · BMC Genomics
  59. The YH database: the first Asian diploid genome database
    Gang Li, Lijia Ma, C. Song, Z. Yang, X. Wang, H. Huang, Yanping Li, Ran Li, X. Zhang, Huanming Yang et al. · 2008 · Nucleic Acids Research
  60. Mapping the human reference genome's missing sequence by three-way admixture in Latino genomes.
    G. Genovese, R. Handsaker, Heng Li, E. Kenny, S. Mccarroll · 2013 · American Journal of Human Genetics
  61. Haplotype-assisted accurate non-invasive fetal whole genome recovery through maternal plasma sequencing
    Sheng‐Pei Chen, Huijuan Ge, Xuebin Wang, Xiaoyu Pan, Xiaotian Yao, Xuchao Li, Chunlei Zhang, Fang Chen, Fuman Jiang, Peipei Li et al. · 2013 · Genome Medicine
  62. Communicating results in post-Belmont era biomonitoring studies: Lessons from genetics and neuroimaging research
    Rachel A. Morello-Frosch, Julia Varshavsky, Max Liboiron, Phil Brown, Julia Green Brody · 2014 · Environmental Research
  63. Functional Genomics Applied to Cardiovascular Medicine
    Thomas P. Cappola, Kenneth B. Margulies · 2011 · Circulation
  64. RelocaTE2: a high resolution transposable element insertion site mapping tool for population resequencing
    Jinfeng Chen, Travis Wrightsman, Susan R. Wessler, Jason Stajich · 2017 · PeerJ
  65. Now is the Time for a Postracial Medicine: Biomedical Research, the National Institutes of Health, and the Perpetuation of Scientific Racism
    Javier Perez-Rodriguez, Alejandro de la Fuente · 2017 · The American Journal of Bioethics
  66. Quantitative Analysis of Single Nucleotide Polymorphisms within Copy Number Variation
    Soohyun Lee, Simon Kasif, Zhiping Weng, Charles R. Cantor · 2008 · PLoS ONE
  67. The thousand‐dollar genome
    Howard Wolinsky · 2007 · EMBO Reports
  68. Challenges in Medical Applications of Whole Exome/Genome Sequencing Discoveries
    Ali J. Marian · 2012 · Trends in Cardiovascular Medicine
  69. How Segmental Duplications Shape Our Genome: Recent Evolution of ABCC6 and PKD1 Mendelian Disease Genes
    Orsolya Symmons, András Váradi, Tamás Arányi · 2008 · Molecular Biology and Evolution
  70. A Male with Unilateral Microphthalmia Reveals a Role for TMX3 in Eye Development
    Ryan Chao, Linda M Nevin, Pooja Agarwal, Jan Riemer, Xiaoyang Bai, Allen D. Delaney, Matthew Akana, Nelson JimenezLopez, Tanya Bardakjian, Adele S. Schneider et al. · 2010 · PLoS ONE
  71. Association Studies in an Era of Too Much Information
    Joseph Loscalzo · 2007 · Circulation
  72. Entailing the Next-Generation Sequencing and Metabolome for Sustainable Agriculture by Improving Plant Tolerance
    Muhammad Furqan Ashraf, Dan Hou, Quaid Hussain, Muhammad Imran, Jialong Pei, Mohsin Ali, Aamar Shehzad, Muhammad Anwar, Ali Noman, Muhammad Waseem et al. · 2022 · International Journal of Molecular Sciences
  73. Genes, culture, and scientific racism
    K. Lala, Marcus W. Feldman · 2024 · Proceedings of the National Academy of Sciences of the United States of America
  74. Next-generation sequencing of vertebrate experimental organisms
    Dann Turner, Thomas Keane, Ian M. Sudbery, David J. Adams · 2009 · Mammalian Genome
  75. Local alignment of two-base encoded DNA sequence
    Nils Homer, Barry Merriman, Stanley F. Nelson · 2009 · BMC Bioinformatics
  76. Single-Stranded Annealing Induced by Re-Initiation of Replication Origins Provides a Novel and Efficient Mechanism for Generating Copy Number Expansion via Non-Allelic Homologous Recombination
    Kenneth J. Finn, Joachim J. Li · 2013 · PLoS Genetics
  77. Human copy number polymorphic genes
    Jeffrey A. Bailey, Jeffrey M. Kidd, Evan E. Eichler · 2008 · Cytogenetic and Genome Research
  78. Genetic basis of transcriptome differences between the founder strains of the rat HXB/BXH recombinant inbred panel
    Marieke Simonis, Santosh S. Atanur, Sam E.V. Linsen, Victor Guryev, Frans-Paul Ruzius, Laurence Gamé, Nico R. Lansu, Ewart de Bruijn, Sebastiaan van Heesch, Steven J.M. Jones et al. · 2012 · Genome biology
  79. Selection of Recombinant Antibodies from Antibody Gene Libraries
    Michael Hust, André Frenzel, Thomas Schirrmann, Stefan Dübel · 2013 · Methods in molecular biology
  80. The haplo-spliceo-transcriptome: common variations in alternative splicing in the human population
    Brenton R. Graveley · 2007 · Trends in Genetics
  81. Population sequencing of two endocannabinoid metabolic genes identifies rare and common regulatory variants associated with extreme obesity and metabolite level
    Olivier Harismendy, Vikas Bansal, Gaurav Bhatia, Masakazu Nakano, Michael Scott, Xiaoyun Wang, Colette Dib, Edouard Turlotte, Jack C. Sipe, Sarah Murray et al. · 2010 · Genome biology
  82. Genome sequence and global sequence variation map with 5.5 million SNPs in Chinese rhesus macaque
    Xiaodong Fang, Yanfeng Zhang, Rui Zhang, Lixin Yang, Ming Li, Kaixiong Ye, Xiaosen Guo, Jun Wang, Bing Su · 2011 · Genome biology
  83. LINE-1 and Alu Methylation Patterns in Lymph Node Metastases of Head and Neck Cancers
    Nakarin Kitkumthorn, Somboon Keelawat, Prakasit Rattanatanyong, Apiwat Mutirangura · 2012 · Asian Pacific Journal of Cancer Prevention
  84. Nature’s Genetic Gradients and the Clinical Phenotype
    Ali J. Marian · 2009 · Circulation Cardiovascular Genetics
  85. High-speed and high-ratio referential genome compression
    Yuansheng Liu, Hui Peng, Limsoon Wong, Jinyan Li · 2017 · Bioinformatics
  86. Polymorphisms in the hepatic lipase gene affect plasma HDL-cholesterol levels in a Turkish population
    Uğur Hodoğlugil, David W. Williamson, Robert W. Mahley · 2009 · Journal of Lipid Research
  87. BAK1 gene variation and abdominal aortic aneurysms
    Bruce Gottlieb, Lorraine E. Chalifour, Benjamin Mitmaker, Nathan Sheiner, Daniel I. Obrand, Cherrie Abraham, Melissa Meilleur, Tomoko Sugahara, Ghassan Bkaily, Morris Schweitzer · 2009 · Human Mutation
  88. Human genome at ten: The sequence explosion
    2010 · Nature
  89. A genome-wide scan for copy number variations using high-density single nucleotide polymorphism array in Simmental cattle
    Yang Wu, Huizhong Fan, Shengyun Jing, Jiangwei Xia, Yan Chen, Lupei Zhang, Xue Gao, Junya Li, Huijiang Gao, Hongyan Ren · 2015 · Animal Genetics
  90. Validation and Genotyping of Multiple Human Polymorphic Inversions Mediated by Inverted Repeats Reveals a High Degree of Recurrence
    Cristina Aguado, Magdalena Gayà‐Vidal, Sergi Villatoro, Meritxell Oliva, David Izquierdo, Carla Giner-Delgado, Víctor Edwin Oré Montalvo, Judit García‐González, Alexander Martinez‐Fundichely, Laia Capilla et al. · 2014 · PLoS Genetics
  91. Massively Parallel Sequencing of Chikso (Korean Brindle Cattle) to Discover Genome-Wide SNPs and InDels
    Jung-Woo Choi, Xiaoping Liao, Sairom Park, Heoyn-Jeong Jeon, Won‐Hyong Chung, Paul Stothard, Yeon-Soo Park, Jeongkoo Lee, Kyung‐Tai Lee, Sang‐Hwan Kim et al. · 2013 · Molecules and Cells
  92. Sequencing and assembly of highly heterozygous genome of Vitis vinifera L. cv Pinot Noir: Problems and solutions
    Andrey Zharkikh, Michela Troggio, Dmitry Pruss, Alessandro Cestaro, Glenn Eldrdge, Massimo Pindo, Jeff T. Mitchell, Silvia Vezzulli, Satish Bhatnagar, Paolo Fontana et al. · 2008 · Journal of Biotechnology
  93. GenHap: a novel computational method based on genetic algorithms for haplotype assembly
    Andrea Tangherloni, Simone Spolaor, Leonardo Rundo, Marco Salvatore Nobile, Paolo Cazzaniga, Giancarlo Mauri, Píetro Lió, Ivan Merelli A, Daniela Besozzi · 2019 · BMC Bioinformatics
  94. Twenty-First Century Precision Medicine in Oncology: Genomic Profiling in Patients With Cancer
    Mitesh J. Borad, Patricia Mucci LoRusso · 2017 · Mayo Clinic Proceedings
  95. Intellectual Disability & Rare Disorders: A Diagnostic Challenge
    Malin Kvarnung, Ann Nordgren · 2017 · Advances in experimental medicine and biology
  96. Ranbow: A fast and accurate method for polyploid haplotype reconstruction
    M-Hossein Moeinzadeh, Jun Mo Yang, Evgeny Muzychenko, Giuseppe Gallone, David Heller, Knut Reinert, Stefan A. Haas, Martin Vingron · 2020 · PLoS Computational Biology
  97. OrthoCluster
    Xinghuo Zeng, Matthew J. Nesbitt, Jian Pei, Ke Wang, Ismael A. Vergara, Nansheng Chen · 2008 · International Conference on Extending Database Technology (EDBT)
  98. Bi-Directional SIFT Predicts a Subset of Activating Mutations
    William Lee, Yan Zhang, Kiran Mukhyala, Robert A. Lazarus, Zemin Zhang · 2009 · PLoS ONE
  99. Performance of High-Throughput Sequencing for the Discovery of Genetic Variation Across the Complete Size Spectrum
    Andy Wing Chun Pang, Jeffrey R. MacDonald, Ryan K. C. Yuen, Vanessa M. Hayes, Stephen W. Scherer · 2013 · G3 Genes Genomes Genetics
  100. SPUMONI 2: improved classification using a pangenome index of minimizer digests
    Omar Ahmed, Massimiliano Rossi, Travis Gagie, Christina A. Boucher, Ben Langmead · 2023 · Genome biology