Genetics-Genomics-Knowledge

Wednesday, 26 June 2013

The Human Genome Contracts Again

http://bioinformatics.oxfordjournals.org/content/early/2013/06/22/bioinformatics.btt362.short?rss=1&utm_content=buffer094f0&utm_source=buffer&utm_medium=twitter&utm_campaign=Buffer

Posted by YourDigitalKnowledgeFinder at 08:42
Email ThisBlogThis!Share to XShare to FacebookShare to Pinterest

No comments:

Post a Comment

Newer Post Older Post Home
Subscribe to: Post Comments (Atom)

Popular Posts

  • Cancer genome-sequencing study design
    http://www.nature.com/nrg/journal/v14/n5/full/nrg3445.html
  • RADIA: RNA and DNA Integrated Analysis for Somatic Mutation Detection
    http://arxiv.org/abs/1402.0850
  • FishingCNV: a graphical software package for detecting rare copy number variations in exome-sequencing data
    http://bioinformatics.oxfordjournals.org/content/early/2013/04/24/bioinformatics.btt151.short?rss=1&buffer_share=c5ca4&utm_source=bu...
  • From FastQ Data to High-Confidence Variant Calls: The Genome Analysis Toolkit Best Practices Pipeline - Current Protocols in Bioinformatics - Auwera - Wiley Online Library
    http://onlinelibrary.wiley.com/doi/10.1002/0471250953.bi1110s43/abstract;jsessionid=FF13D61431F1B7A0666A3D6C0B4173E1.f03t01
  • Whole-genome sequencing identifies genetic alterations in pediatric low-grade gliomas : Nature Genetics : Nature Publishing Group
    http://www.nature.com/ng/journal/vaop/ncurrent/full/ng.2611.html
  • eXtasy: Variant Prioritization
    http://homes.esat.kuleuven.be/~bioiuser/eXtasy/?utm_source=twitterfeed&utm_medium=twitter
  • Genome Biology | Abstract | Transcriptome analysis of human tissues and cell lines reveals one dominant transcript per gene
    http://genomebiology.com/2013/14/7/R70/abstract
  • WEB TOOL Sequence Coverage
    http://seqcoverage.com/
  • Best SED tutorial for ever
    http://www.grymoire.com/Unix/Sed.html
  • fastq-tools
    I am browsing [fastq-tools]. Have a look at it! http://homes.cs.washington.edu/~dcjones/fastq-tools/?utm_content=buffer7e4f0&utm_medium=...

Blog Archive

  • ►  2015 (2)
    • ►  June (1)
    • ►  March (1)
  • ►  2014 (44)
    • ►  December (1)
    • ►  November (1)
    • ►  September (2)
    • ►  August (4)
    • ►  July (5)
    • ►  June (7)
    • ►  March (4)
    • ►  February (9)
    • ►  January (11)
  • ▼  2013 (146)
    • ►  December (21)
    • ►  November (12)
    • ►  October (10)
    • ►  September (16)
    • ►  August (11)
    • ►  July (12)
    • ▼  June (17)
      • Sean Davis - R Tutorials
      • Identification of deleterious synonymous variants ...
      • The Human Genome Contracts Again
      • The cancer genome in context: of mice and mutation...
      • What is sashimi_plot? — MISO 1.0 documentation
      • GAT: a simulation framework for testing the associ...
      • [NGS] False Positives from Next-Gen Sequencing | M...
      • [NGS] BMC Bioinformatics | Abstract | Benchmarking...
      • DMEAS: DNA Methylation Entropy Analysis Software
      • eXtasy: Variant Prioritization
      • BMC Genomics | Abstract | Web-based visual analysi...
      • European Journal of Human Genetics - The Genome of...
      • Exome Sequencing Scientific Publications
      • PLOS ONE: A Novel Classification of Lung Cancer in...
      • The 1000 Genomes Project: paving the way for perso...
      • PyroHMMsnp: an SNP caller for Ion Torrent and 454 ...
      • PLOS ONE: IMSA: Integrated Metagenomic Sequence An...
    • ►  May (15)
    • ►  April (32)
Simple theme. Theme images by gaffera. Powered by Blogger.

About Me

YourDigitalKnowledgeFinder
View my complete profile