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Proceedings of the USENIX ... Annual Technical Conference. USENIX Technical Conference
|
September 28, 2011
Free Factories: Unified Infrastructure for Data Intensive Web Services
Alexander Wait Zaranek, Tom Clegg, Ward Vandewege, et al.
Plos Genetics
|
June 10, 2010
A survey of genomic traces reveals a common sequencing error, RNA editing, and DNA editing
Alexander Wait Zaranek, Erez Y Levanon, Tomer Zecharia, et al.
Bioinformatics (Oxford, England)
|
June 25, 2009
Swift: primary data analysis for the Illumina Solexa sequencing platform
Nava Whiteford, Tom Skelly, Christina Curtis, et al.
Genome Research
|
June 16, 2009
Multiplex padlock targeted sequencing reveals human hypermutable CpG variations
Jin Billy Li, Yuan Gao, John Aach, et al.
Gigascience
|
October 12, 2016
The whole genome sequences and experimentally phased haplotypes of over 100 personal genomes
Qing Mao, Serban Ciotlos, Rebecca Yu Zhang, et al.
Nature
|
July 13, 2012
Accurate whole-genome sequencing and haplotyping from 10 to 20 human cells
Brock A Peters, Bahram G Kermani, Andrew B Sparks, et al.
Lancet (London, England)
|
May 4, 2010
Clinical assessment incorporating a personal genome
Euan A Ashley, Atul J Butte, Matthew T Wheeler, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 17, 2012
A public resource facilitating clinical use of genomes
Madeleine P Ball, Joseph V Thakuria, Alexander Wait Zaranek, et al.
Nature
|
July 10, 2009
A highly annotated whole-genome sequence of a Korean individual
Jong-Il Kim, Young Seok Ju, Hansoo Park, et al.
Science (New York, N.Y.)
|
November 7, 2009
Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays
Radoje Drmanac, Andrew B Sparks, Matthew J Callow, et al.
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Search research articles
Search
Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
Proceedings of the USENIX ... Annual Technical Conference. USENIX Technical Conference
|
September 28, 2011
Free Factories: Unified Infrastructure for Data Intensive Web Services
Alexander Wait Zaranek, Tom Clegg, Ward Vandewege, et al.
Plos Genetics
|
June 10, 2010
A survey of genomic traces reveals a common sequencing error, RNA editing, and DNA editing
Alexander Wait Zaranek, Erez Y Levanon, Tomer Zecharia, et al.
Bioinformatics (Oxford, England)
|
June 25, 2009
Swift: primary data analysis for the Illumina Solexa sequencing platform
Nava Whiteford, Tom Skelly, Christina Curtis, et al.
Genome Research
|
June 16, 2009
Multiplex padlock targeted sequencing reveals human hypermutable CpG variations
Jin Billy Li, Yuan Gao, John Aach, et al.
Gigascience
|
October 12, 2016
The whole genome sequences and experimentally phased haplotypes of over 100 personal genomes
Qing Mao, Serban Ciotlos, Rebecca Yu Zhang, et al.
Nature
|
July 13, 2012
Accurate whole-genome sequencing and haplotyping from 10 to 20 human cells
Brock A Peters, Bahram G Kermani, Andrew B Sparks, et al.
Lancet (London, England)
|
May 4, 2010
Clinical assessment incorporating a personal genome
Euan A Ashley, Atul J Butte, Matthew T Wheeler, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 17, 2012
A public resource facilitating clinical use of genomes
Madeleine P Ball, Joseph V Thakuria, Alexander Wait Zaranek, et al.
Nature
|
July 10, 2009
A highly annotated whole-genome sequence of a Korean individual
Jong-Il Kim, Young Seok Ju, Hansoo Park, et al.
Science (New York, N.Y.)
|
November 7, 2009
Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays
Radoje Drmanac, Andrew B Sparks, Matthew J Callow, et al.
Page
of 1