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Genome Biology
Results: 5930

#	Item
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! ! Add to Reading List Source URL: www.bionanogenomics.com Language: English - Date: 2015-02-19 13:11:33 Bioinformatics Genetic mapping Molecular biology Contig Genome project Human genome Gene mapping Cell DNA Biology Genetics Genomics
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 Add to Reading List Source URL: www.sagescience.com Language: English - Date: 2014-04-25 15:39:25 Genomics DNA sequencing Biotechnology DNA Full genome sequencing Contig Sequencing Genome Biology Genetics Molecular biology
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 Add to Reading List Source URL: www.bionanogenomics.com Language: English - Date: 2015-05-04 16:12:35 Molecular biology Genetic mapping DNA sequencing Genome project Human genome Genome Reference genome Copy-number variation Shotgun sequencing Biology Genetics Genomics
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 Add to Reading List Source URL: biologyinternational.org Language: English - Date: 2011-03-04 12:57:55 Genomics Population genetics Medical genetics Human genetics International Union of Biological Sciences Human genome Cousin marriage Full genome sequencing Human Genome Project Biology Genetics Philosophy of biology
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 Add to Reading List Source URL: bioinformatica.uab.es Language: English - Date: 2007-05-08 05:35:18 Genetic genealogy DNA Genome projects Recent single origin hypothesis Neanderthal genome project Neanderthal Ancient DNA Human genome Mitochondrial Eve Genetics Biology Human evolution
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. Add to Reading List Source URL: www.uni-regensburg.de Language: English - Date: 2015-04-08 02:42:25 Molecular biology Epigenetics Bioinformatics DNA Exome sequencing Epigenomics Full genome sequencing Metabolome Epigenome Biology Genetics Genomics
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 Add to Reading List Source URL: www.fsma.org.hk Language: English - Date: 2013-04-29 02:31:53 Motor neurone disease Spinal muscular atrophy RNA splicing Applied genetics Biotechnology SMN1 Antisense therapy Survival of motor neuron SMN2 Genetics Biology Spliceosome
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 Add to Reading List Source URL: macarthurlab.files.wordpress.com Language: English - Date: 2014-07-21 14:38:14 Molecular biology Biological databases Genomics Indel Genomes Project DbSNP Human genome Single-nucleotide polymorphism International HapMap Project Biology Genetics Bioinformatics
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 Add to Reading List Source URL: sfi.nr.no Language: English - Date: 2014-10-12 16:58:07 Molecular biology DNA sequencing Epigenetics MicroRNA Illumina DNA methylation RNA-Seq The Cancer Genome Atlas Oncotype DX Genetics Biology RNA
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 Add to Reading List Source URL: macarthurlab.files.wordpress.com Language: English* - Date: 2014-07-21 14:36:45 Molecular biology DNA Bioinformatics Human genome Full genome sequencing Genomes Project Gene Pseudogene Ridge Biology Genetics Genomics

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