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  2. RNA-Seq - Wikipedia

    en.wikipedia.org/wiki/RNA-Seq

    Gene length: Longer genes will have more fragments/reads/counts than shorter genes if transcript expression is the same. This is adjusted by dividing the FPM by the length of a feature (which can be a gene, transcript, or exon), resulting in the metric fragments per kilobase of feature per million mapped reads (FPKM). [90]

  3. Molecular-weight size marker - Wikipedia

    en.wikipedia.org/wiki/Molecular-weight_size_marker

    The restriction fragments are then ligated together. [31] A molecular marker is then generated when specific fragments are selected for amplification. AFLP markers are run alongside a DNA marker on a gel. A common AFLP DNA marker is 30-330bp long. [32] The fragments of this marker lie at 10bp intervals to increase precision. RAPD

  4. Read (biology) - Wikipedia

    en.wikipedia.org/wiki/Read_(biology)

    Sequencing technologies vary in the length of reads produced. Reads of length 20-40 base pairs (bp) are referred to as ultra-short. [2] Typical sequencers produce read lengths in the range of 100-500 bp. [3] However, Pacific Biosciences platforms produce read lengths of approximately 1500 bp. [4] Read length is a factor which can affect the results of biological studies. [5]

  5. DNA sequencing - Wikipedia

    en.wikipedia.org/wiki/DNA_sequencing

    In 2012, with cameras operating at more than 10 MHz A/D conversion rates and available optics, fluidics and enzymatics, throughput can be multiples of 1 million nucleotides/second, corresponding roughly to 1 human genome equivalent at 1x coverage per hour per instrument, and 1 human genome re-sequenced (at approx. 30x) per day per instrument ...

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

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

    Flow chart for Hi-C data analysis. [29] Paired-end reads are first iteratively mapped to a reference genome. Mapped reads are then assigned to a restriction fragment/genomic loci, with fragment-level filtering. Data is then binned, filtered at the bin level, and then balanced to correct for potential biases. [29] [30]

  7. Genome size - Wikipedia

    en.wikipedia.org/wiki/Genome_size

    Genome size ranges (in base pairs) of various life forms. Genome size is the total amount of DNA contained within one copy of a single complete genome.It is typically measured in terms of mass in picograms (trillionths or 10 −12 of a gram, abbreviated pg) or less frequently in daltons, or as the total number of nucleotide base pairs, usually in megabases (millions of base pairs, abbreviated ...

  8. Electropherogram - Wikipedia

    en.wikipedia.org/wiki/Electropherogram

    The method plots data points that represent a specific time and fluorescence intensity at various wavelengths of light to represent a DNA profile. [ 2 ] [ page needed ] In the field of genetics, an electropherogram is a plot of DNA fragment sizes, typically used for genotyping such as DNA sequencing . [ 3 ]

  9. Minimal genome - Wikipedia

    en.wikipedia.org/wiki/Minimal_genome

    The minimal genome corresponds to small genome sizes, as bacterial genome size correlates with the number of protein-coding genes, typically one gene per kilobase. [1] Mycoplasma genitalium , with a 580 kb genome and 482 protein-coding genes, is a key model for minimal genomes.