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  2. Transcriptomics technologies - Wikipedia

    en.wikipedia.org/wiki/Transcriptomics_technologies

    An expressed sequence tag (EST) is a short nucleotide sequence generated from a single RNA transcript. RNA is first copied as complementary DNA (cDNA) by a reverse transcriptase enzyme before the resultant cDNA is sequenced. [ 16 ]

  3. Expressed sequence tag - Wikipedia

    en.wikipedia.org/wiki/Expressed_sequence_tag

    Alternatively, if the genome of the organism that originated the EST has been sequenced, one can align the EST sequence to that genome using a computer. The current understanding of the human set of genes (as of 2006) includes the existence of thousands of genes based solely on EST evidence. In this respect, ESTs have become a tool to refine ...

  4. Bioinformatics - Wikipedia

    en.wikipedia.org/wiki/Bioinformatics

    Systems biology involves the use of computer simulations of cellular subsystems (such as the networks of metabolites and enzymes that comprise metabolism, signal transduction pathways and gene regulatory networks) to both analyze and visualize the complex connections of these cellular processes.

  5. Genome survey sequence - Wikipedia

    en.wikipedia.org/wiki/Genome_survey_sequence

    Genome survey sequencing is a new way to map the genome sequences since it is not dependent on mRNA.Current genome sequencing approaches are mostly high-throughput shotgun methods, and GSS is often used on the first step of sequencing.

  6. Contig - Wikipedia

    en.wikipedia.org/wiki/Contig

    A contig (from contiguous) is a set of overlapping DNA segments that together represent a consensus region of DNA. [1] In bottom-up sequencing projects, a contig refers to overlapping sequence data (); [2] in top-down sequencing projects, contig refers to the overlapping clones that form a physical map of the genome that is used to guide sequencing and assembly. [3]

  7. Cap analysis of gene expression - Wikipedia

    en.wikipedia.org/wiki/Cap_Analysis_of_Gene...

    In 2013, Batut et al. [13] combined CAP trapper, template switching, and 5′-phosphate-dependent exonuclease digestion in RAMPAGE to maximize promoter specificity. In 2014, Murata et al. [ 14 ] published the nAnTi-CAGE protocol, where capped 5′ ends are sequenced on the Illumina platform with no PCR amplification and no tag cleavage.

  8. Expected progeny difference - Wikipedia

    en.wikipedia.org/wiki/Expected_Progeny_Difference

    Expected progeny differences (EPD) are an evaluation of an animal’s genetic worth as a parent. They are based on animal models which combine all information known about an individual and its relatives to create a genetic profile of the animal’s merits.

  9. Amplicon - Wikipedia

    en.wikipedia.org/wiki/Amplicon

    In molecular biology, an amplicon is a piece of DNA or RNA that is the source and/or product of amplification or replication events. It can be formed artificially, using various methods including polymerase chain reactions (PCR) or ligase chain reactions (LCR), or naturally through gene duplication .