検索結果 - Mark Chaisson
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lra: A long read aligner for sequences and contigs 著者: Jingwen Ren, Mark Chaisson
出版事項 2021Artigo -
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Short read fragment assembly of bacterial genomes 著者: Mark Chaisson, Pavel A. Pevzner
出版事項 2007Artigo -
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Genetic variation and the de novo assembly of human genomes 著者: Mark Chaisson, Richard K. Wilson, Evan E. Eichler
出版事項 2015Revisão -
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Reconstructing complex regions of genomes using long-read sequencing technology 著者: John Huddleston, Swati Ranade, Maika Malig, Francesca Antonacci, Mark Chaisson, Lawrence Hon, Peter H. Sudmant, Tina Graves, Can Alkan, Megan Y. Dennis, Richard K. Wilson, Stephen W. Turner, Jonas Korlach, Evan E. Eichler
出版事項 2014Artigo -
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Resolving the complexity of the human genome using single-molecule sequencing 著者: Mark Chaisson, John Huddleston, Megan Y. Dennis, Peter H. Sudmant, Maika Malig, Fereydoun Hormozdiari, Francesca Antonacci, Urvashi Surti, Richard Sandstrom, Matthew Boitano, Jane M. Landolin, J Stamatoyannopoulos, Michael W. Hunkapiller, Jonas Korlach, Evan E. Eichler
出版事項 2014Artigo -
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Discovery and genotyping of structural variation from long-read haploid genome sequence data 著者: John Huddleston, Mark Chaisson, Karyn Meltz Steinberg, Wes Warren, Kendra Hoekzema, David Gordon, Tina A. Graves-Lindsay, Katherine M. Munson, Zev Kronenberg, Laura Vives, Paul Peluso, Matthew Boitano, Chen-Shin Chin, Jonas Korlach, Richard K. Wilson, Evan E. Eichler
出版事項 2016Artigo -
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Long-read sequence assembly of the gorilla genome 著者: David Gordon, John Huddleston, Mark Chaisson, C. Hill, Zev Kronenberg, Katherine M. Munson, Maika Malig, Archana N. Raja, Ian T. Fiddes, LaDeana Hillier, Christopher Dunn, Carl Baker, Joel Armstrong, Mark Diekhans, Benedict Paten, Jay Shendure, Richard K. Wilson, David Haussler, Chen-Shan Chin, Evan E. Eichler
出版事項 2016Artigo -
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Fully phased human genome assembly without parental data using single-cell strand sequencing and long reads 著者: David Porubský, Peter Ebert, Peter A. Audano, Mitchell R. Vollger, William T. Harvey, Pierre Marijon, Jana Ebler, Katherine M. Munson, Melanie Sorensen, Arvis Sulovari, Marina Haukness, Maryam Ghareghani, Peter M. Lansdorp, Benedict Paten, Scott E. Devine, Ashley D. Sanders, Charles Lee, Mark Chaisson, Jan O. Korbel, Evan E. Eichler, Tobias Marschall
出版事項 2020Artigo -
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Expectations and blind spots for structural variation detection from long-read assemblies and short-read genome sequencing technologies 著者: Xuefang Zhao, Ryan L. Collins, Wan‐Ping Lee, Alexandra M. Weber, Yukyung Jun, Qihui Zhu, Ben Weisburd, Yongqing Huang, Peter A. Audano, Harold Wang, Mark Walker, Chelsea Lowther, Jack Fu, Mark Gerstein, Scott E. Devine, Tobias Marschall, Jan O. Korbel, Evan E. Eichler, Mark Chaisson, Charles Lee, Ryan E. Mills, Harrison Brand, Michael E. Talkowski
出版事項 2021Artigo -
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Scalable Nanopore sequencing of human genomes provides a comprehensive view of haplotype-resolved variation and methylation 著者: Mikhail Kolmogorov, Kimberley J. Billingsley, Mira Mastoras, Melissa Meredith, Jean Monlong, Ryan Lorig-Roach, Mobin Asri, Pilar Álvarez Jerez, Laksh Malik, Ramita Dewan, Xylena Reed, Rylee M. Genner, Kensuke Daida, Sairam Behera, Kishwar Shafin, Trevor Pesout, Jeshuwin Prabakaran, P. Carnevali, Jianzhi Yang, Arang Rhie, Sonja W. Scholz, Bryan J. Traynor, Karen H. Miga, Miten Jain, Winston Timp, Adam M. Phillippy, Mark Chaisson, Fritz J. Sedlazeck, Cornelis Blauwendraat, Benedict Paten
出版事項 2023Pré-impressão -
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Scalable Nanopore sequencing of human genomes provides a comprehensive view of haplotype-resolved variation and methylation 著者: Mikhail Kolmogorov, Kimberley J. Billingsley, Mira Mastoras, Melissa Meredith, Jean Monlong, Ryan Lorig-Roach, Mobin Asri, Pilar Álvarez Jerez, Laksh Malik, Ramita Dewan, Xylena Reed, Rylee M. Genner, Kensuke Daida, Sairam Behera, Kishwar Shafin, Trevor Pesout, Jeshuwin Prabakaran, P. Carnevali, Jianzhi Yang, Arang Rhie, Sonja W. Scholz, Bryan J. Traynor, Karen H. Miga, Miten Jain, Winston Timp, Adam M. Phillippy, Mark Chaisson, Fritz J. Sedlazeck, Cornelis Blauwendraat, Benedict Paten
出版事項 2023Artigo
関連主題
Biology
Genetics
Gene
Genome
Computational biology
Human genome
Computer science
Structural variation
Gene expression
Reference genome
DNA sequencing
Genotype
Haplotype
Single-nucleotide polymorphism
Transcriptome
1000 Genomes Project
Evolutionary biology
Sequence assembly
Human genetic variation
Whole genome sequencing
Algorithm
Indel
Tandem repeat
Allele
Hybrid genome assembly
Physics
Programming language
Astrophysics
Contig
Database