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  2. Compression of genomic sequencing data - Wikipedia

    en.wikipedia.org/wiki/Compression_of_genomic...

    While standard data compression tools (e.g., zip and rar) are being used to compress sequence data (e.g., GenBank flat file database), this approach has been criticized to be extravagant because genomic sequences often contain repetitive content (e.g., microsatellite sequences) or many sequences exhibit high levels of similarity (e.g., multiple genome sequences from the same species).

  3. Human genome - Wikipedia

    en.wikipedia.org/wiki/Human_genome

    The completed human genome sequence will also provide better understanding of human formation as an individual organism and how humans vary both between each other and other species. [ 68 ] Although the 'completion' of the human genome project was announced in 2001, [ 2 ] there remained hundreds of gaps, with about 5–10% of the total sequence ...

  4. CRAM (file format) - Wikipedia

    en.wikipedia.org/wiki/CRAM_(file_format)

    Compressed Reference-oriented Alignment Map (CRAM) is a compressed columnar file format for storing biological sequences aligned to a reference sequence, initially devised by Markus Hsi-Yang Fritz et al. [1] CRAM was designed to be an efficient reference-based alternative to the Sequence Alignment Map (SAM) and Binary Alignment Map (BAM) file ...

  5. Human Genome Project - Wikipedia

    en.wikipedia.org/wiki/Human_Genome_Project

    The Human Genome Project (HGP) was an international scientific research project with the goal of determining the base pairs that make up human DNA, and of identifying, mapping and sequencing all of the genes of the human genome from both a physical and a functional standpoint.

  6. Scaffolding (bioinformatics) - Wikipedia

    en.wikipedia.org/wiki/Scaffolding_(bioinformatics)

    Most high-throughput, next generation sequencing platforms produce shorter read lengths compared to Sanger sequencing.These new platforms are able to generate large quantities of data in short periods of time, but until methods were developed for de novo assembly of large genomes from short read sequences, Sanger sequencing remained the standard method of creating a reference genome. [10]

  7. GeneCards - Wikipedia

    en.wikipedia.org/wiki/GeneCards

    To gather these scattered data, the Weizmann Institute of Science's Crown Human Genome Centre developed a database called ‘GeneCards’ in 1997. This database mainly dealt with human genome information, human genes, the encoded proteins’ functions, and related diseases, though it has expanded since that time.

  8. UniProt - Wikipedia

    en.wikipedia.org/wiki/UniProt

    UniProt is a freely accessible database of protein sequence and functional information, many entries being derived from genome sequencing projects.It contains a large amount of information about the biological function of proteins derived from the research literature.

  9. 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 (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 ...