Genetics-Genomics-Knowledge

Sunday, 16 February 2014

Functional annotation of noncoding sequence variants : Nature Methods : Nature Publishing Group

http://www.nature.com/nmeth/journal/vaop/ncurrent/full/nmeth.2832.html

Posted by YourDigitalKnowledgeFinder at 09:16 No comments:
Email ThisBlogThis!Share to XShare to FacebookShare to Pinterest

Tuesday, 11 February 2014

SplicePlot: a tool for visualizing alternative splicing -- splice_plot 1.0 documentation

http://montgomerylab.stanford.edu/spliceplot/

Posted by YourDigitalKnowledgeFinder at 20:36 No comments:
Email ThisBlogThis!Share to XShare to FacebookShare to Pinterest

Monday, 10 February 2014

Genome Biology | Abstract | Using high-density DNA methylation arrays to profile copy number alterations

http://genomebiology.com/2014/15/2/R30/abstract

Posted by YourDigitalKnowledgeFinder at 06:50 No comments:
Email ThisBlogThis!Share to XShare to FacebookShare to Pinterest

Sunday, 9 February 2014

JAMA Network | From Genome-Wide Association Studies to Next-Generation Sequencing: Lessons From the Past and Planning for the Future

http://archneur.jamanetwork.com/article.aspx?articleid=1763963

Posted by YourDigitalKnowledgeFinder at 20:22 No comments:
Email ThisBlogThis!Share to XShare to FacebookShare to Pinterest

Tuesday, 4 February 2014

RADIA: RNA and DNA Integrated Analysis for Somatic Mutation Detection

http://arxiv.org/abs/1402.0850

Posted by YourDigitalKnowledgeFinder at 21:05 No comments:
Email ThisBlogThis!Share to XShare to FacebookShare to Pinterest

PLOS Genetics: Single Cell Genomics: Advances and Future Perspectives


http://www.plosgenetics.org/article/info:doi%2F10.1371%2Fjournal.pgen.1004126

Posted by YourDigitalKnowledgeFinder at 07:27 No comments:
Email ThisBlogThis!Share to XShare to FacebookShare to Pinterest

Monday, 3 February 2014

From single-cell to cell-pool transcriptomes: Stochasticity in gene expression and RNA splicing

http://m.genome.cshlp.org/content/early/2014/01/30/gr.161034.113.abstract

Posted by YourDigitalKnowledgeFinder at 06:31 No comments:
Email ThisBlogThis!Share to XShare to FacebookShare to Pinterest

A general framework for estimating the relative pathogenicity of human genetic variants : Nature Genetics : Nature Publishing Group

http://www.nature.com/ng/journal/vaop/ncurrent/full/ng.2892.html

Posted by YourDigitalKnowledgeFinder at 06:23 No comments:
Email ThisBlogThis!Share to XShare to FacebookShare to Pinterest

Sunday, 2 February 2014

BMC Bioinformatics | Abstract | Inferring clonal evolution of tumors from single nucleotide somatic mutations

http://www.biomedcentral.com/1471-2105/15/35/abstract

Posted by YourDigitalKnowledgeFinder at 20:10 No comments:
Email ThisBlogThis!Share to XShare to FacebookShare to Pinterest
Newer Posts Older Posts Home
Subscribe to: Posts (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)
      • Functional annotation of noncoding sequence varian...
      • SplicePlot: a tool for visualizing alternative spl...
      • Genome Biology | Abstract | Using high-density DNA...
      • JAMA Network | From Genome-Wide Association Studie...
      • RADIA: RNA and DNA Integrated Analysis for Somatic...
      • PLOS Genetics: Single Cell Genomics: Advances and ...
      • From single-cell to cell-pool transcriptomes: Stoc...
      • A general framework for estimating the relative pa...
      • BMC Bioinformatics | Abstract | Inferring clonal e...
    • ►  January (11)
  • ►  2013 (146)
    • ►  December (21)
    • ►  November (12)
    • ►  October (10)
    • ►  September (16)
    • ►  August (11)
    • ►  July (12)
    • ►  June (17)
    • ►  May (15)
    • ►  April (32)
Simple theme. Theme images by gaffera. Powered by Blogger.

About Me

YourDigitalKnowledgeFinder
View my complete profile