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  2. 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]

  3. 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

  4. Hi-C (genomic analysis technique) - Wikipedia

    en.wikipedia.org/wiki/Hi-C_(genomic_analysis...

    Any platform that can allow for the ligated fragments to be sequenced across the NheI junction (Roche 454) or by paired-end or mate-paired reads (Illumina GA and HiSeq platforms) would be suitable for Hi-C. [4] Before high-throughput sequencing, the quality of the library should be verified using Sanger sequencing, wherein the long sequencing ...

  5. Carlson curve - Wikipedia

    en.wikipedia.org/wiki/Carlson_Curve

    The Carlson curve is a term to describe the rate of DNA sequencing or cost per sequenced base as a function of time. [1] It is the biotechnological equivalent of Moore's law . Carlson predicted that the doubling time of DNA sequencing technologies (measured by cost and performance) would be at least as fast as Moore's law.

  6. Tiling array - Wikipedia

    en.wikipedia.org/wiki/Tiling_array

    The other way of synthesizing tiling array chips is via mechanically printing probes onto the chip. This is done by using automated machines with pins that place the previously synthesized probes onto the surface. Due to the size restriction of the pins, these chips can hold up to nearly 400,000 features. [4]

  7. ChIP-on-chip - Wikipedia

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

    The cost of the DNA microarrays is often a limiting factor to whether a laboratory should proceed with a ChIP-on-chip experiment. Another limitation is the size of DNA fragments that can be achieved. Most ChIP-on-chip protocols utilize sonication as a method of breaking up DNA into small pieces.

  8. Ion semiconductor sequencing - Wikipedia

    en.wikipedia.org/wiki/Ion_semiconductor_sequencing

    The cost of acquiring a pH-mediated sequencer at time of launch was priced at around $50,000 USD, excluding sample preparation equipment and a server for data analysis. [8] [11] [15] The cost per run is also significantly lower than that of alternative automated sequencing methods, at roughly $1,000. [8] [12]

  9. Peak calling - Wikipedia

    en.wikipedia.org/wiki/Peak_calling

    Wilbanks and colleagues [3] is a survey of the ChIP-seq peak callers, and Bailey et al. [4] is a description of practical guidelines for peak calling in ChIP-seq data. Peak calling may be conducted on transcriptome/exome as well to RNA epigenome sequencing data from MeRIPseq [ 5 ] or m6Aseq [ 6 ] for detection of post-transcriptional RNA ...

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