Results for "Genome"

Tags

  • Map genome-wide DNA double-strand breaks using next generation sequencing http://breakome.utmb.edu/Home.html #DNA #Breaks #Chromosome #Sequencing #Genome

    Tags: DNA, Breaks, Chromosome, Sequencing, Genome

    3425 days ago

  • Genomic burden http://www.nature.com/news/genomes-carry-a-heavy-burden-1.17304 #Genome #Burden #Mutation #Disease

    Tags: Genome, Burden, Mutation, Disease

    3355 days ago

  • LASTZ

    LASTZ is a program for aligning DNA sequences, a pairwise aligner. Originally designed to handle sequences the size of human chromosomes and from different species, it is also useful for sequences produced by NGS sequencing technologies such as Roche 454. More at http://www.bx.psu.edu/~rsharris/...

    Tags: Bioinformatics, NGS, Comparative Genomics, Genome, LASTZ

    2989 days ago

  • How does the 3D genome technology works?

    There are many techniques available to enquire about the oganization of the nucleus. I am keenly interested to know the basic machanism behind it. I mean how does it works?

    Tags: Mate pair sequencing, Paired end sequencing, Sequencing, Genomics, NGS, Technology, Genome, 3D Genome

    3323 days ago

  • Hi-C browser http://hic.umassmed.edu/welcome/welcome.php#Browser #HiC #Genome #Interation

    Tags: HiC, Genome, Interation

    3322 days ago

  • Gene analysis has made easier http://www.ebi.ac.uk/about/news/press-releases/gwas-analysis-made-easier #Gene #GWAS #Genome #Traits

    Tags: Gene, GWAS, Genome, Traits

    3296 days ago

  • Software packages for next gen sequence analysis

    Integrated solutions * CLCbio Genomics Workbench - de novo and reference assembly of Sanger, Roche FLX, Illumina, Helicos, and SOLiD data. Commercial next-gen-seq software that extends the CLCbio Main Workbench software. Includes SNP detection, CHiP-seq, browser and other features. Commercial. Wi...

    Tags: Bioinformatics, Computational Biology, Education, Assemblied, Sequence, Genome, Align, Software, SNP

    3292 days ago

  • Sequencing By Xpansion

    Sequencing By Xpansion (SBX) is a DNA sequencing method that uses a simple biochemical reaction to encode the sequence of a DNA molecule into a highly measurable surrogate called an Xpandomer. This single molecule approach produces enough Xpandomer in a single drop reaction to sequence an entire ...

    Tags: Bioinformatics, Computational Biology, Education, Sequence, Seq, Genome, Xpansion

    3294 days ago

  • Genome data resources http://zhanggj.cngb.org/home/?page_id=1297 #Genome #Data #Genomics

    Tags: Genome, Data, Genomics

    3289 days ago

  • The next 20 years of genome research http://biorxiv.org/content/biorxiv/early/2015/06/02/020289.full.pdf #Genome #Research #Future

    Tags: Genome, Research, Future

    3289 days ago