991![Mapping and De Novo Assembly of Long Barcoded Molecule of DNA from a Cancer Genome J. Reifenberger, Z. Dzakula, V. Dergachev, T. Anantharaman, A. Hastie, S. Chan, H. Cao ! BioNano Genomics, San Diego, CA, USA! ! Mapping and De Novo Assembly of Long Barcoded Molecule of DNA from a Cancer Genome J. Reifenberger, Z. Dzakula, V. Dergachev, T. Anantharaman, A. Hastie, S. Chan, H. Cao ! BioNano Genomics, San Diego, CA, USA! !](https://www.pdfsearch.io/img/1d5682f818c0cb77f6ccb665e8ae1807.jpg) | Add to Reading ListSource URL: www.bionanogenomics.comLanguage: English - Date: 2015-02-19 13:11:33
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992![Case Study :: Mount Sinai Precise Sizing and SMRT Sequencing Offer Unprecedented Read Length for Clinical Studies At the Icahn Institute for Genomics and Multiscale Biology, scientists use automated DNA sizing together Case Study :: Mount Sinai Precise Sizing and SMRT Sequencing Offer Unprecedented Read Length for Clinical Studies At the Icahn Institute for Genomics and Multiscale Biology, scientists use automated DNA sizing together](https://www.pdfsearch.io/img/b00f1a2c514996df953bab47c60b1f95.jpg) | Add to Reading ListSource URL: www.sagescience.comLanguage: English - Date: 2014-04-25 15:39:25
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993![Mapping the “Dark Matter” of Genome – Long Repeats, Structural Variations in Complex Cancer Genome with Nanochannel Technology A Hastie1, E Lam1, A Pang1, W Andrews1, T Anantharaman1, T Chan1, M Saghibini1, H Sadow Mapping the “Dark Matter” of Genome – Long Repeats, Structural Variations in Complex Cancer Genome with Nanochannel Technology A Hastie1, E Lam1, A Pang1, W Andrews1, T Anantharaman1, T Chan1, M Saghibini1, H Sadow](https://www.pdfsearch.io/img/d435a0902a033858082022e4de26002e.jpg) | Add to Reading ListSource URL: www.bionanogenomics.comLanguage: English - Date: 2015-05-04 16:12:35
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994![Cytosine methylation is a chemical modification of DNA which can be faithfully inherited. contrarily to base substitution mutations, this DNA modification does not change the pairing properties of the modified base. C-me Cytosine methylation is a chemical modification of DNA which can be faithfully inherited. contrarily to base substitution mutations, this DNA modification does not change the pairing properties of the modified base. C-me](https://www.pdfsearch.io/img/27522afef0dc8f7ef780c7d34225db1b.jpg) | Add to Reading ListSource URL: biologyinternational.orgLanguage: English - Date: 2011-03-04 12:57:55
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995![Vol 444 | 16 November 2006 | doi:nature05336 ARTICLES Analysis of one million base pairs of Neanderthal DNA Richard E. Green1, Johannes Krause1, Susan E. Ptak1, Adrian W. Briggs1, Michael T. Ronan2, Jan F. Simon Vol 444 | 16 November 2006 | doi:nature05336 ARTICLES Analysis of one million base pairs of Neanderthal DNA Richard E. Green1, Johannes Krause1, Susan E. Ptak1, Adrian W. Briggs1, Michael T. Ronan2, Jan F. Simon](https://www.pdfsearch.io/img/f73657f38601819d6ccdd23e9d1c47de.jpg) | Add to Reading ListSource URL: bioinformatica.uab.esLanguage: English - Date: 2007-05-08 05:35:18
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996![Dear colleagues, we warmly welcome you to the 5th Workshop of Genetic Epidemiology in the Hotel St. Georg, Bad Aibling (see below). We are looking forward to compelling talks and discussions. Dear colleagues, we warmly welcome you to the 5th Workshop of Genetic Epidemiology in the Hotel St. Georg, Bad Aibling (see below). We are looking forward to compelling talks and discussions.](https://www.pdfsearch.io/img/49ed9194164dbe118c1a06b5378fcd8d.jpg) | Add to Reading ListSource URL: www.uni-regensburg.deLanguage: English - Date: 2015-04-08 02:42:25
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997![npg Call in the backup The most common genetic killer of infants, a disease known as spinal muscular atrophy, is caused by mutations in a single gene. The human genome contains its own backup system—near-identical cop npg Call in the backup The most common genetic killer of infants, a disease known as spinal muscular atrophy, is caused by mutations in a single gene. The human genome contains its own backup system—near-identical cop](https://www.pdfsearch.io/img/d4266e5f944e4f45eaa96dc6585a3ec8.jpg) | Add to Reading ListSource URL: www.fsma.org.hkLanguage: English - Date: 2013-04-29 02:31:53
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998![A systematic survey of loss-of-function variants in human protein-coding genes Supplementary material Daniel G. MacArthur, Suganthi Balasubramanian, Adam Frankish, Ni Huang, James Morris, Klaudia Walter, Luke Jostins, Lu A systematic survey of loss-of-function variants in human protein-coding genes Supplementary material Daniel G. MacArthur, Suganthi Balasubramanian, Adam Frankish, Ni Huang, James Morris, Klaudia Walter, Luke Jostins, Lu](https://www.pdfsearch.io/img/779f63415e214cc1e8d409f59e46577f.jpg) | Add to Reading ListSource URL: macarthurlab.files.wordpress.comLanguage: English - Date: 2014-07-21 14:38:14
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999![comprehensive genomic breast cancer databases: Norwegian breast cancer study (NBCS) The Norwegian breast cancer study possesses detailed molecular data (see Table) with unique patient follow up provided by the comprehensive genomic breast cancer databases: Norwegian breast cancer study (NBCS) The Norwegian breast cancer study possesses detailed molecular data (see Table) with unique patient follow up provided by the](https://www.pdfsearch.io/img/b071570524bc29ecd09a533f2dfcf4ea.jpg) | Add to Reading ListSource URL: sfi.nr.noLanguage: English - Date: 2014-10-12 16:58:07
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1000![A systematic survey of loss-of-function variants in human protein-coding genes Daniel G. MacArthur1,2,*, Suganthi Balasubramanian3,4, Adam Frankish1, Ni Huang1, James Morris1, Klaudia Walter1, Luke Jostins1, Lukas Habegg A systematic survey of loss-of-function variants in human protein-coding genes Daniel G. MacArthur1,2,*, Suganthi Balasubramanian3,4, Adam Frankish1, Ni Huang1, James Morris1, Klaudia Walter1, Luke Jostins1, Lukas Habegg](https://www.pdfsearch.io/img/e68b5f96b7fd55e2e384924bf8a8f6af.jpg) | Add to Reading ListSource URL: macarthurlab.files.wordpress.comLanguage: English - Date: 2014-07-21 14:36:45
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