The Diploid Genome Sequence of an Individual Human

Cited by (1,000)

Items 201–300 of 1,000

  1. Interpretation of Genomic Variants Using a Unified Biological Network Approach
    Ekta Khurana, Yao Fu, Jieming Chen, Mark Gerstein · 2013 · PLoS Computational Biology
  2. The draft genome of the carcinogenic human liver fluke Clonorchis sinensis
    Xiaoyun Wang, Wenjun Chen, Yan Huang, Jiufeng Sun, Jingtao Men, Hailiang Liu, Fang Luo, Lei Guo, Xiaoli Lv, Chuanhuan Deng et al. · 2011 · Genome biology
  3. High-throughput genome scaffolding from in vivo DNA interaction frequency
    Noam Kaplan, Job Dekker · 2013 · Nature Biotechnology
  4. Genes, mutations, and human inherited disease at the dawn of the age of personalized genomics
    D.N. Cooper, Jian‐Min Chen, Edward V. Ball, Katy Howells, Matthew E. Mort, Andrew D. Phillips, Nadia A Chuzhanova, Michael Krawczak, Hildegard Kehrer‐Sawatzki, Peter D. Stenson · 2010 · Human Mutation
  5. The clinical context of copy number variation in the human genome
    Charles Lee, Stephen W. Scherer · 2010 · Expert Reviews in Molecular Medicine
  6. Intentions to receive individual results from whole-genome sequencing among participants in the ClinSeq study
    Flavia M. Facio, Haley R. Eidem, Tyler C. Fisher, Stephanie P. Brooks, Amy Linn, Kimberly A. Kaphingst, Leslie G. Biesecker, Barbara Bowles Biesecker · 2012 · European Journal of Human Genetics
  7. From Human Genetics and Genomics to Pharmacogenetics and Pharmacogenomics: Past Lessons, Future Directions
    Daniel W. Nebert, Ge Zhang, Elliot S. Vesell · 2008 · Drug Metabolism Reviews
  8. The pursuit of genome-wide association studies: where are we now?
    Chee‐Seng Ku, En Yun Loy, Yudi Pawitan Y, Kee Seng Chia · 2010 · Journal of Human Genetics
  9. Depletion of the AD Risk Gene SORL1 Selectively Impairs Neuronal Endosomal Traffic Independent of Amyloidogenic APP Processing
    Allison Knupp, Swati Mishra, Refugio A. Martinez, Jacquelyn E. Braggin, Marcell P. Szabo, Chizuru Kinoshita, Dale W. Hailey, Scott A. Small, Suman Jayadev, Jessica E. Young · 2020 · Cell Reports
  10. Mining and Development of Novel SSR Markers Using Next Generation Sequencing (NGS) Data in Plants
    Sima Taheri, Thohirah Lee Abdullah, Mohd Yusop Rafii, Mohamed Musa Hanafi, Mahbod Sahebi, Parisa Azizi, Redmond Ramin Shamshiri · 2018 · Molecules
  11. The presenilin-1 ΔE9 mutation results in reduced γ-secretase activity, but not total loss of PS1 function, in isogenic human stem cells
    Woodruff, Grace, Young, Jessica E., Martinez, Fernando J., Buen, Floyd, Gore, Athurva, Kinaga, Jennifer, Li, Zhe, Yuan, Shauna H., Zhang, Kun, Goldstein, Lawrence S.B. · 2013 · Cell Reports
  12. Advantages and limitations of next‐generation sequencing technologies: A comparison of electrophoresis and non‐electrophoresis methods
    Daniel G. Hert, Christopher P. Fredlake, Annelise E. Barron · 2008 · Electrophoresis
  13. Hybrid selection of discrete genomic intervals on custom-designed microarrays for massively parallel sequencing
    Emily C. Hodges, Michelle G. Rooks, Zhenyu Xuan, Arindam Bhattacharjee, D. Benjamin Gordon, Leonardo Brizuela, William Richard McCombie, Gregory J. Hannon · 2009 · Nature Protocols
  14. High-resolution human genome structure by single-molecule analysis
    Brian P. Teague, Michael S. Waterman, Steven Goldstein, Konstantinos D. Potamousis, Shiguo Zhou, Susan Reslewic, Deepayan Sarkar, Anton Valouev, Christopher Churas, Jeffrey M. Kidd et al. · 2010 · Proceedings of the National Academy of Sciences
  15. The immunoglobulin heavy chain locus: genetic variation, missing data, and implications for human disease
    Corey T. Watson, Felix J. Breden · 2012 · Genes and Immunity
  16. Evolution of an adenocarcinoma in response to selection by targeted kinase inhibitors
    Steven J.M. Jones, Janessa J. Laskin, Yvonne Y. Li, Obi L. Griffith, Jianghong An, Mikhail Bilenky, Yaron S.N. Butterfield, Timothée Cezard, Eric Chuah, Richard Corbett et al. · 2010 · Genome biology
  17. Genetic architecture of colorectal cancer
    Ulrike Peters, Stephanie A. Bien, Niha Zubair · 2015 · Gut
  18. Novel variation and de novo mutation rates in population-wide de novo assembled Danish trios
    Søren Besenbacher, SiYang Maggie Liu, José M. G. Izarzugaza, Jakob Grove, Kirstine Belling, Jette Bork‐Jensen, Shujia Huang, Thomas D. Als, Shengting Li, Rachita Yadav et al. · 2015 · Nature Communications
  19. What's in a name? Y chromosomes, surnames and the genetic genealogy revolution
    Turi E. King, Mark A. Jobling · 2009 · Trends in Genetics
  20. Copy number variation in the bovine genome
    João Fadista, Bo Thomsen, Lars‐Erik Holm, Christian Bendixen · 2010 · BMC Genomics
  21. A geometric approach for classification and comparison of structural variants
    Suzanne Sindi, Elena Helman, Ali Bashir, Benjamin J. Raphael · 2009 · Bioinformatics
  22. Archaic human ancestry in East Asia
    Pontus Skoglund, Mattias Jakobsson · 2011 · Proceedings of the National Academy of Sciences
  23. Prediction of individual genetic risk of complex disease
    Naomi R. Wray, Michael Edward Goddard, Peter M. Visscher · 2008 · Current Opinion in Genetics & Development
  24. Bacteria-Human Somatic Cell Lateral Gene Transfer Is Enriched in Cancer Samples
    David R. J. Riley, Karsten B. Sieber, Kelly M. Robinson, James Robert White, Ashwinkumar Ganesan, Syrus Nourbakhsh, Julie C. Dunning Hotopp · 2013 · PLoS Computational Biology
  25. Multiple personal genomes await
    J. Craig Venter · 2010 · Nature
  26. Genomic microarrays in mental retardation: from copy number variation to gene, from research to diagnosis
    Lisenka E.L.M. Vissers, Bert B A De Vries, Joris A. Veltman · 2009 · Journal of Medical Genetics
  27. MicroRNAs and the skin: Tiny players in the body's largest organ
    Michael S. Sand, Thilo Gambichler, Daniel Sand, Marina Skrygan, Peter Josef Altmeyer, Falk G. Bechara · 2008 · Journal of Dermatological Science
  28. Genomic drift and copy number variation of sensory receptor genes in humans
    Masafumi Nozawa, Yoshihiro Kawahara, Masatoshi Nei · 2007 · Proceedings of the National Academy of Sciences
  29. A Wide Extent of Inter-Strain Diversity in Virulent and Vaccine Strains of Alphaherpesviruses
    MORIAH LOUISE SZPARA, Yolanda R. Tafuri, Lance R. Parsons, S. Rafi Shamim, Kevin J. Verstrepen, Matthieu Legendre, Lynn W. Enquist · 2011 · PLoS Pathogens
  30. Frequent and Efficient Use of the Sister Chromatid for DNA Double-Strand Break Repair during Budding Yeast Meiosis
    Tamara Goldfarb, Michael Lichten · 2010 · PLoS Biology
  31. The Characterization of Twenty Sequenced Human Genomes
    Kimberly Pelak, Kevin V. Shianna, Dongliang Ge, Jessica M. Maia, Mingfu Zhu, Jason P. Smith, Elizabeth T. Cirulli, Jacques Fellay, Samuel P. Dickson, Curtis E. Gumbs et al. · 2010 · PLoS Genetics
  32. Natural Selection Affects Multiple Aspects of Genetic Variation at Putatively Neutral Sites across the Human Genome
    Kirk E. Lohmueller, Anders Albrechtsen, Yingrui Li, Su Yeon Kim, Thorfinn Sand Korneliussen, Nicolas Vinckenbosch, Geng Tian, Emilia Huerta‐Sánchez, Alison F. Feder, Niels Grarup et al. · 2011 · PLoS Genetics
  33. Ensembl Genome Browser
    Xosé M. Fernández, Ewan Birney · 2009 · Springer eBooks
  34. Assessing structural variation in a personal genome—towards a human reference diploid genome
    Adam C. English, William J. Salerno, Oliver A. Hampton, Claudia G. Gonzaga-Jauregui, Shruthi Ambreth, Deborah Ritter, Christine R. Beck, Caleb Davis, Mahmoud Dahdouli, Singer Ma et al. · 2015 · BMC Genomics
  35. SNP detection and genotyping from low-coverage sequencing data on multiple diploid samples
    Si Quang Le, Richard Michael Durbin · 2010 · Genome Research
  36. Genomic sequencing of single microbial cells from environmental samples
    Thomas Ishoey, Tanja Woyke, Ramūnas Stepanauskas, Mark A. Novotny, Roger S. Lasken · 2008 · Current Opinion in Microbiology
  37. Deterministic and Stochastic Allele Specific Gene Expression in Single Mouse Blastomeres
    Fuchou Tang, Cátálin Bárbácioru, Ellen Nordman, Siqin Bao, Caroline Guat Lay Lee, Xiaohui Wang, Brian Benjamin Tuch, Édith Heard, Kaiqin Lao, M. Azim Surani · 2011 · PLoS ONE
  38. Molecular genetic studies of complex phenotypes
    Ali J. Marian · 2011 · Translational research
  39. The next-generation sequencing technology and application
    Xiaoguang Zhou, Lufeng Ren, Qingshu Meng, Yuntao Li, Yude Yu, Jun Myoung Yu · 2010 · Protein & Cell
  40. Characterization of missing human genome sequences and copy-number polymorphic insertions
    Jeffrey M. Kidd, Nick Sampas, Francesca Antonacci, Tina Graves, Robert S. Fulton, Hillary S. Hayden, Can Alkan, Maika Malig, Mario Ventura, Giuliana Giannuzzi et al. · 2010 · Nature Methods
  41. Pharmacogenetics and pharmacogenomics of anticancer agents
    R. Stephanie Huang, Mark J. Ratain · 2009 · CA A Cancer Journal for Clinicians
  42. Identification of copy number variations and common deletion polymorphisms in cattle
    Joon Seol Bae, Hyun Sub Cheong, Lyoung Hyo Kim, Suk NamGung, Tae Joon Park, Ji-Yong Chun, Yongha Kim, Charisse Flerida A. Pasaje, Jin Sol Lee, Hyoung Doo Shin · 2010 · BMC Genomics
  43. Pervasive Multinucleotide Mutational Events in Eukaryotes
    Daniel R. Schrider, Jonathan Hourmozdi, Matthew W. Hahn · 2011 · Current Biology
  44. Analysis of copy number variants and segmental duplications in the human genome: Evidence for a change in the process of formation in recent evolutionary history
    Philip M. Kim, Hugo Y. K. Lam, Alexander Eckehart Urban, Jan O. Korbel, Jason P. Affourtit, Fabian Grubert, Xueying Chen, Sherman M. Weissman, Michael P. Snyder, Mark Gerstein · 2008 · Genome Research
  45. The challenges and importance of structural variation detection in livestock
    Derek M. Bickhart, George E. Liu · 2014 · Frontiers in Genetics
  46. Extensive Copy-Number Variation of the Human Olfactory Receptor Gene Family
    Janet M. Young, RaeLynn M. Endicott, Sean S Parghi, Megan Walker, Jeffrey M. Kidd, Barbara J. Trask · 2008 · The American Journal of Human Genetics
  47. On Jim Watson's APOE status: genetic information is hard to hide
    Dale R. Nyholt, Chang‐En Yu, Peter M. Visscher · 2008 · European Journal of Human Genetics
  48. Extensive genomic and transcriptional diversity identified through massively parallel DNA and RNA sequencing of eighteen Korean individuals
    Young Seok Ju, Jong‐Il Kim, Sheehyun Kim, Dongwan Hong, Hansoo Park, Jong-Yeon Shin, Seungbok Lee, Won‐Chul Lee, Su-Jung Kim, Saet-Byeol Yu et al. · 2011 · Nature Genetics
  49. UMD‐Predictor: A High‐Throughput Sequencing Compliant System for Pathogenicity Prediction of any Human cDNA Substitution
    David Salgado, Jean‐Pierre Desvignes, Ghadi Raï, Arnaud Blanchard, Morgane Miltgen, Amélie Pinard, Nicolas Lévy, Gwenaëlle Collod‐Béroud, Christophe Béroud · 2016 · Human Mutation
  50. Personal genome sequencing: current approaches and challenges
    Michael P. Snyder, Jiang Du, Mark Gerstein · 2010 · Genes & Development
  51. Genomics Really Gets Personal: How Exome and Whole Genome Sequencing Challenge the Ethical Framework of Human Genetics Research
    H. Tabor, Benjamin E. Berkman, S. Hull, M. Bamshad · 2011 · American Journal of Medical Genetics. Part A
  52. Omics Technologies, Data and Bioinformatics Principles
    Maria Victoria Schneider, Sandra E. Orchard · 2011 · Methods in molecular biology
  53. MicroRNAs in skin and wound healing
    Jaideep Banerjee, Yuk Cheung Chan, Chandan K. Sen · 2010 · Physiological Genomics
  54. An integrative probabilistic model for identification of structural variation in sequencing data
    Suzanne Sindi, Selim Önal, Luke Peng, Hsin-Ta Wu, Benjamin J. Raphael · 2012 · Genome biology
  55. Enhancer deletions of the SHOX gene as a frequent cause of short stature: the essential role of a 250 kb downstream regulatory domain
    J Chen, Gabi Wildhardt, Zeyan Zhong, R Röth, B Weiss, Daniela Steinberger, Jochen Decker, Werner Friedrich Blum, Gudrun Rappold · 2009 · Journal of Medical Genetics
  56. Epigenetic Control of Retrotransposon Expression in Human Embryonic Stem Cells
    Ángela Macia, Martín Muñoz-López, José Luis Cortés, Robert K. Hastings, Santiago Morell, Gema Lucena-Aguilar, Juan Antonio Marchal, Richard M. Badge, Jose Luis Garcia-Perez · 2010 · Molecular and Cellular Biology
  57. Introduction: Race, Genetics, and Disease
    Joan H. Fujimura, Troy Duster, Ramya M. Rajagopalan · 2008 · Social Studies of Science
  58. Structural variation in two human genomes mapped at single-nucleotide resolution by whole genome de novo assembly
    Yingrui Li, Hancheng Zheng, Ruibang Luo, Honglong Wu, Hongmei Zhu, Ruiqiang Li, Hongzhi Cao, Boxin Wu, Shujia Huang, Haojing Shao et al. · 2011 · Nature Biotechnology
  59. Human chromosome‐specific aneuploidy is influenced by DNA‐dependent centromeric features
    Marie Dumont, Riccardo Gamba, Pierre Gestraud, Sjoerd J. Klaasen, Joseph T Worrall, Sippe G. de Vries, Vincent G. Boudreau, Catalina Salinas‐Luypaert, Paul S. Maddox, Susanne M. A. Lens et al. · 2019 · The EMBO Journal
  60. Consensus generation and variant detection by Celera Assembler
    Gennady Denisov, Brian P. Walenz, Aaron L. Halpern, Jason Rafe Miller, Nelson Axelrod, Samuel Levy, Granger Sutton · 2008 · Bioinformatics
  61. Human inversions and their functional consequences
    Marta Puig, Sònia Casillas, Sergi Villatoro, Mario Cáceres · 2015 · Briefings in Functional Genomics
  62. A human scFv antibody generation pipeline for proteome research
    Michael Hust, Torsten Meyer, Bernd Voedisch, Torsten Rülker, Holger Thie, Aymen El-Ghezal, Martina Inga Kirsch, Mark Schütte, Saskia Helmsing, Doris Meier et al. · 2010 · Journal of Biotechnology
  63. Genetics and Genomics for the Prevention and Treatment of Cardiovascular Disease: Update
    Santhi K. Ganesh, Donna K. Arnett, Themistocles L. Assimes, Craig T. Basson, Aravinda Chakravarti, Patrick T. Ellinor, Mary B. Engler, Elizabeth Goldmuntz, David M. Herrington, Ray E. Hershberger et al. · 2013 · Circulation
  64. Salivary Genomics, Transcriptomics and Proteomics: The Emerging Concept of the Oral Ecosystem and their Use in the Early Diagnosis of Cancer and other Diseases
    T Fábián, P Fejérdy, Péter Csermely · 2008 · Current Genomics
  65. Characteristics of de novo structural changes in the human genome
    Wigard P. Kloosterman, Laurent C. Francioli, Fereydoun Hormozdiari, Tobias Marschall, Jayne Y. Hehir‐Kwa, Abdel Abdellaoui, Eric-Wubbo Lameijer, Matthijs H. Moed, Vyacheslav Koval, Ivo Renkens et al. · 2015 · Genome Research
  66. Contribution of rare and common variants determine complex diseases—Hirschsprung disease as a model
    Maria M. Alves, Yunia Sribudiani, Rutger W. W. Brouwer, Jeanne Amiel, Guillermo Antiñolo, Salud Borrego, Isabella Ceccherini, Aravinda Chakravarti, Raquel M. Fernández, María-Mercé García-Barceló et al. · 2013 · Developmental Biology
  67. Methods for Genomic Partitioning
    Emily H. Turner, Sarah Boon Hsi Ng, Deborah A. Nickerson, Jay Shendure · 2009 · Annual Review of Genomics and Human Genetics
  68. Pseudomitochondrial genome haunts disease studies: Table 1
    Y-G Yao, Q-P Kong, Antonio Salas, H-J Bandelt · 2008 · Journal of Medical Genetics
  69. Integrity of the human centromere DNA repeats is protected by CENP-A, CENP-C, and CENP-T
    Simona Giunta, Hironori Funabiki · 2017 · Proceedings of the National Academy of Sciences
  70. The Alzheimer’s gene SORL1 is a regulator of endosomal traffic and recycling in human neurons
    Swati Mishra, Allison Knupp, Marcell P. Szabo, Charles A. Williams, Chizuru Kinoshita, Dale W. Hailey, Yuliang Wang, Olav M. Andersen, Jessica E. Young · 2022 · Cellular and Molecular Life Sciences
  71. Clinical Utility of Contemporary Molecular Cytogenetics
    Bassem A. Bejjani, Lisa G. Shaffer · 2008 · Annual Review of Genomics and Human Genetics
  72. An MCMC algorithm for haplotype assembly from whole-genome sequence data
    Vikas Bansal, Aaron L. Halpern, Nelson Axelrod, Vineet Bafna · 2008 · Genome Research
  73. Optimal algorithms for haplotype assembly from whole-genome sequence data
    Dan He, Arthur Choi, Knot Pipatsrisawat, Adnan Y. Darwiche, Eleazar Eskin · 2010 · Bioinformatics
  74. Whole-genome and whole-exome sequencing in neurological diseases
    Jia Nee Foo, Jianjun Liu, Eng‐King Tan · 2012 · Nature Reviews Neurology
  75. PRISM: Pair-read informed split-read mapping for base-pair level detection of insertion, deletion and structural variants
    Yue Jiang, Yadong Wang, Michael Brudno · 2012 · Bioinformatics
  76. HapCompass: A Fast Cycle Basis Algorithm for Accurate Haplotype Assembly of Sequence Data
    Derek Aguiar, Sorin Istrail · 2012 · Journal of Computational Biology
  77. Unravelling the genetics of inherited retinal dystrophies: Past, present and future
    Suzanne Broadgate, Jing Yu, Susan M. Downes, Stephanie Halford · 2017 · Progress in Retinal and Eye Research
  78. Phage Display for the Generation of Antibodies for Proteome Research, Diagnostics and Therapy
    Thomas Schirrmann, Torsten Meyer, Mark Schütte, André Frenzel, Michael Hust · 2011 · Molecules
  79. Detection and characterization of novel sequence insertions using paired-end next-generation sequencing
    Iman Hajirasouliha, Fereydoun Hormozdiari, Can Alkan, Jeffrey M. Kidd, İnanç Birol, Evan E. Eichler, S. Cenk Şahinalp · 2010 · Bioinformatics
  80. Non-crossover gene conversions show strong GC bias and unexpected clustering in humans
    Amy L. Williams, Giulio Genovese, Thomas D. Dyer, Nicolas Altemose, Katherine Truax, Goo Jun, Nick J. Patterson, Simon Robert Myers, Joanne E. Curran, Ravi Duggirala et al. · 2015 · eLife
  81. Efficient identification of Y chromosome sequences in the human and Drosophila genomes
    Antonio Bernardo Carvalho, Andrew G. Clark · 2013 · Genome Research
  82. The human Major Histocompatibility Complex as a paradigm in genomics research
    Claire Vandiedonck, Julian Charles Knight · 2009 · Briefings in Functional Genomics and Proteomics
  83. DNA replication timing and higher-order nuclear organization determine single nucleotide substitution patterns in cancer genomes
    Lin L. Liu, S. De, F. Michor · 2013 · Nature Communications
  84. Informed consent for whole genome sequencing: A qualitative analysis of participant expectations and perceptions of risks, benefits, and harms
    Holly K. Tabor, Jacquie Stock, Tracy Brazg, Margaret J. McMillin, Karin M. Dent, Joon‐Ho Yu, Jay Shendure, Michael J. Bamshad · 2012 · American Journal of Medical Genetics Part A
  85. The Promise of Radio Analytics: A Future Paradigm of Wireless Positioning, Tracking, and Sensing
    Beibei Wang, Qinyi Xu, Chen Chen, Feng Zhang, K. J. Ray Liu · 2018 · IEEE Signal Processing Magazine
  86. Proteogenomics
    Santosh Renuse, Raghothama Chaerkady, Akhilesh Pandey · 2010 · PROTEOMICS
  87. A Palindrome-Mediated Recurrent Translocation with 3:1 Meiotic Nondisjunction: The t(8;22)(q24.13;q11.21)
    Molly B. Sheridan, Takema Kato, Chad R. Haldeman‐Englert, G. Reza Jalali, Jeff M. Milunsky, Ying S. Zou, Ruediger Klaes, G. Gimelli, Stefania Gimelli, Robert M. Gemmill et al. · 2010 · The American Journal of Human Genetics
  88. Identification of novel FMR1 variants by massively parallel sequencing in developmentally delayed males
    Stephen C. Collins, Steven M. Bray, Joshua A. Suhl, David J. Cutler, Bradford W. Coffee, Michael E. Zwick, Stephen T. Warren · 2010 · American Journal of Medical Genetics Part A
  89. Systematic discovery of complex insertions and deletions in human cancers
    Kai Ye, Jiayin Wang, Reyka G. Jayasinghe, Eric-Wubbo Lameijer, Joshua F. McMichael, Jie Ning, Michael D. McLellan, Mingchao Xie, Song Cao, Venkata D. Yellapantula et al. · 2015 · Nature Medicine
  90. The discovery of human genetic variations and their use as disease markers: past, present and future
    Chee‐Seng Ku, En Yun Loy, Agus Salim, Yudi Pawitan Y, Kee Seng Chia · 2010 · Journal of Human Genetics
  91. Whole-genome sequencing and comprehensive variant analysis of a Japanese individual using massively parallel sequencing
    Akihiro Fujimoto, Hidewaki Nakagawa, Naoya Hosono, Kaoru Nakano, Tetsuo Abe, Keith A. Boroevich, Masao Nagasaki, Rui Yamaguchi, Tetsuo Shibuya, Michiaki Kubo et al. · 2010 · Nature Genetics
  92. Detection of Clinically Relevant Copy Number Variants with Whole-Exome Sequencing
    Joep de Ligt, Philip M. Boone, Rolph Pfundt, Lisenka E.L.M. Vissers, Todd Richmond, Joel M. Geoghegan, Kathleen O'Moore, Nicole de Leeuw, Christine J. Shaw, Han G. Brunner et al. · 2013 · Human Mutation
  93. Searching NCBI's dbSNP Database
    Medha Bhagwat · 2010 · Current Protocols in Bioinformatics
  94. High-Resolution Copy-Number Variation Map Reflects Human Olfactory Receptor Diversity and Evolution
    Yehudit Hasin-Brumshtein, Tsviya Olender, Miriam Khen, Claudia G. Gonzaga-Jauregui, Philip M. Kim, Alexander Eckehart Urban, Michael P. Snyder, Mark Gerstein, Doron Lancet, Jan O. Korbel · 2008 · PLoS Genetics
  95. Understanding Incidental Findings in the Context of Genetics and Genomics
    Mildred K. Cho · 2008 · The Journal of Law Medicine & Ethics
  96. Charting the genetic interaction map of a cell
    Michael Costanzo, Anastasia Baryshnikova, Chad L. Myers, Brenda Andrews, Charles M. Boone · 2010 · Current Opinion in Biotechnology
  97. Advances in molecular technology and their impact on fisheries genetics
    Lorenz Hauser, James E. Seeb · 2008 · Fish and Fisheries
  98. Human genome diversity: frequently asked questions
    Guido Barbujani, Vincenza Colonna · 2010 · Trends in Genetics
  99. Ultralow-input single-tube linked-read library method enables short-read second-generation sequencing systems to routinely generate highly accurate and economical long-range sequencing information
    Zhoutao Chen, Long Pham, Tsai-Chin Wu, Guoya Mo, Yu Xia, Peter L. Chang, Devin K. Porter, Tấn Đức Phan, Huu Che, Hao Tran et al. · 2020 · Genome Research
  100. Human genetics and genomics a decade after the release of the draft sequence of the human genome
    Nasheen Naidoo, Yudi Pawitan Y, Richie Soong, D.N. Cooper, Chee‐Seng Ku · 2011 · Human Genomics