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The classic selective sweep or hard sweep is expected to occur when beneficial mutations are rare but when a beneficial mutation that has occurred increases in frequency rapidly, drastically reducing genetic variation in the population. Soft sweeps from standing genetic variation (SGV) occurs when previously neutral mutations that were present ...
FOSDEM —Free and Open-source Software Developers' European Meeting. FOSI —Formatted Output Specification Instance. FOSS —Free and Open-Source Software. FP —Function Programming. FP —Functional Programming. FPGA —Field Programmable Gate Array. FPS —Floating Point Systems. FPU —Floating-Point Unit. FRU —Field-Replaceable Unit.
Copy number variation is a type of structural variation: specifically, it is a type of duplication or deletion event that affects a considerable number of base pairs. [2] Approximately two-thirds of the entire human genome may be composed of repeats [3] and 4.8–9.5% of the human genome can be classified as copy number variations. [4]
An abbreviation for paragraph. gutter A vertical margin of white space where two pages meet, such as in the crease of a book or newspaper. gutter journalism H hard copy Copy that is printed on physical paper, as opposed to soft copy, which exists in digital form. hard news. Also called straight news.
The term "hard copy" predates the digital computer. In the book and newspaper printing process, "hard copy" refers to a manuscript or typewritten document that has been edited and proofread and is ready for typesetting or being read on-air in a radio or television broadcast. The old meaning of hard copy was mostly discarded after the ...
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In book, magazine, and music publishing, a manuscript is an autograph or copy of a work, written by an author, composer or copyist. Such manuscripts generally follow standardized typographic and formatting rules, in which case they can be called fair copy (whether original or copy). The staff paper commonly used for handwritten music is, for ...
Copy number analysis is the process of analyzing data produced by a test for DNA copy number variation in an organism's sample. One application of such analysis is the detection of chromosomal copy number variation that may cause or may increase risks of various critical disorders. [1] [2] Copy number variation can be detected with various ...