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GET TO KNOW YOUR NEIGHBOR ; SDEE 2015 Year End Social on Dec 8th in San Diego ; Must Attend 5-Day Event in San Diego Starting Tomorrow! -- CDW on Cells, Sensors, and Sysems, with Updates on Stem Cells ; SDEE October 2015 Event - Financings: Tales from the Tranches ; Allele Biotech Takes Major Step into Nano Antibody Leadership Position
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NexGen Sequencing, Epigenetics, and Editing
 
 
Analysis of five years of controlled access and data sharing compliance at the International Cancer Genome Consortium
Friday, 03.04.2016, 01:02am

Questions have been raised about whether these data sharing practices carry potential privacy risks for research participants

 

Analysis of computational footprinting methods for DNase sequencing experiments
Tuesday, 03.01.2016, 02:02am
This comparison of ten computational methods for detecting transcription factor binding sites in DNase hypersensitive regions in the genome determines which methods work consistently well, how DNase-seq experimental artifacts should be corrected for and which score is best for ranking methods.
Mammalian NET-seq analysis defines nascent RNA profiles and associated RNA processing genome-wide
Wednesday, 02.17.2016, 11:14pm
mNET-seq generates genome-wide, single-nucleotide–resolution data on Pol II occupancy and co-transcriptional RNA processing, with the unique ability to link these processes to Pol II C-terminal domain phosphorylation states.
Co-occurrence of MYC amplification and TP53 mutations in human cancer
Tuesday, 02.02.2016, 08:58pm
It has frequently been reported that MYCamplifications affect the cell cycle and apoptosis pathway.
Quantification of private information leakage from phenotype-genotype data: linking attacks
Monday, 02.01.2016, 11:45pm
Linking attacks can identify individuals on the basis of seemingly independent data, such as molecular phenotypes and genotypes, in different databases and are a threat to privacy. The authors statistically quantify the extent of this risk and propose means to reduce it.
Improving databases for human variation
Thursday, 01.28.2016, 11:54pm
To determine the true pathogenicity of genetic variants, data sharing is essential.
A diamond in the ruff
Tuesday, 12.29.2015, 07:14pm
The ruff genome sequence papers exemplify three of the most important aspects of a useful genome: new biological insights, a high-quality resource and population variation data.
  » Microbiomes: Curating communities from plants
  » Key mendelian variants
  » Small island, big genetic discoveries
  » Genomics: Acorn worms in a nutshell
  » Small island, big genetic discoveries
  » TARDIS, a targeted RNA directional sequencing method for rare RNA discovery
  » Standardized phenotyping enhances Mendelian disease gene identification
  » Foreign DNA capture during CRISPR–Cas adaptive immunity
  » Gene signatures from pancreatic cancer tumor and stromal cells predict disease outcome
  » Comparing the performance of biomedical clustering methods


 
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::| Hot News
Analysis of five years of controlled access and data sharing compliance at the International Cancer Genome Consortium
Analysis of computational footprinting methods for DNase sequencing experiments
Mammalian NET-seq analysis defines nascent RNA profiles and associated RNA processing genome-wide
Co-occurrence of MYC amplification and TP53 mutations in human cancer
Quantification of private information leakage from phenotype-genotype data: linking attacks
Improving databases for human variation
A diamond in the ruff
Microbiomes: Curating communities from plants
Small island, big genetic discoveries
TARDIS, a targeted RNA directional sequencing method for rare RNA discovery