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  2. Chromatin immunoprecipitation - Wikipedia

    en.wikipedia.org/wiki/Chromatin_immunoprecipitation

    The cost and accessibility of ChIP-seq is a major disadvantage, which has led to the more predominant use of ChIP-chip in laboratories across the world. [2] This photo compares the efficacy of the two experimental techniques, ChIP-seq and ChIP-chip. Table 1 Advantages and disadvantages of NChIP and XChIP

  3. Personal genomics - Wikipedia

    en.wikipedia.org/wiki/Personal_genomics

    The cost of sequencing a human genome is dropping rapidly, due to the continual development of new, faster, cheaper DNA sequencing technologies such as "next-generation DNA sequencing". The National Human Genome Research Institute, an arm of the U.S. National Institutes of Health , has reported that the cost to sequence a whole human-sized ...

  4. ChIP sequencing - Wikipedia

    en.wikipedia.org/wiki/ChIP_sequencing

    The performance of ChIP-seq was then compared to the alternative protein–DNA interaction methods of ChIP-PCR and ChIP-chip. [17] Nucleosome Architecture of Promoters: Using ChIP-seq, it was determined that Yeast genes seem to have a minimal nucleosome-free promoter region of 150bp in which RNA polymerase can initiate transcription. [18]

  5. ChIP-on-chip - Wikipedia

    en.wikipedia.org/wiki/ChIP-on-chip

    Introduced in 2007, ChIP sequencing (ChIP-seq) is a technology that uses chromatin immunoprecipitation to crosslink the proteins of interest to the DNA but then instead of using a micro-array, it uses the more accurate, higher throughput method of sequencing to localize interaction points. [13]

  6. ChIP-exo - Wikipedia

    en.wikipedia.org/wiki/ChIP-exo

    ChIP-exo workflow. ChIP-exo is a chromatin immunoprecipitation based method for mapping the locations at which a protein of interest (transcription factor) binds to the genome. It is a modification of the ChIP-seq protocol, improving the resolution of binding sites from hundreds of base pairs to almost one base pair.

  7. Transcriptomics technologies - Wikipedia

    en.wikipedia.org/wiki/Transcriptomics_technologies

    Sequencing technology platforms commonly used for RNA-Seq [77] [78] Platform Commercial release Typical read length Maximum throughput per run Single read accuracy RNA-Seq runs deposited in the NCBI SRA (Oct 2016) [79] 454 Life Sciences: 2005 700 bp 0.7 Gbp 99.9% 3548 Illumina: 2006 50–300 bp 900 Gbp 99.9% 362903 SOLiD: 2008 50 bp 320 Gbp 99. ...

  8. CUT&Tag sequencing - Wikipedia

    en.wikipedia.org/wiki/CUT&Tag_sequencing

    CUT&Tag is an alternative to the current standard of ChIP-seq. ChIP-Seq suffers from limitations due to the cross linking step in ChIP-Seq protocols that can promote epitope masking and generate false-positive binding sites. [3] [4] As well, ChIP-seq suffers from suboptimal signal-to-noise ratios and poor resolution. [5]

  9. File:Historic cost of sequencing a human genome.svg

    en.wikipedia.org/wiki/File:Historic_cost_of...

    The Wikipedia will use its language if the SVG file supports that language. For example, the German Wikipedia will use German if the SVG file has German. To embed this file in a particular language use the lang parameter with the appropriate language code, e.g. [[File:Historic cost of sequencing a human genome.svg|lang=en]] for