Anagrammen & Informatie over | Engels woord BREAKPOINTS

Voorbeelden van het gebruik van BREAKPOINTS in een zin

• Ectopic recombination is typically mediated by sequence similarity at the duplicate breakpoints, which form direct repeats.
• Paracentric inversions do not include the centromere, and both breakpoints occur in one arm of the chromosome.
• NET Framework applications, a "New Project" wizard, toolbars, menus, panels and a docking system, and built-in code refactoring tools, and it has an integrated debugger that allows for stepping, viewing values of objects in memory, and breakpoints.
• The "D" represented a JTAG TAP for debugging; the "I" denoted an ICEBreaker debug module supporting hardware breakpoints and watchpoints, and letting the system be stalled for debugging.
• The NHC can issue these advisories at one of seven locations along the Pacific coast, known as breakpoints, beginning at the Mexico–United States border, and continuing northward to Point Piedras Blancas.
• Debuggers also commonly allow the use of breakpoints or provide other user interfaces that cause additional source code (such as property accessors) to be executed stealthily, which can, in turn, change the state of the program.
• Unlike in other debuggers, breakpoints can't be set by clicking in the left margin; they must be set via keypress or menu.
• It offers features comparable to source-code debuggers like gdb, including breakpoints, the ability to look at the current context and "memory," and single-stepping through the XSLT.
• A 111-kb copy number gain with breakpoints within the TRK-fused gene (a target of translocations in lymphoma and thyroid tumors) and GPR128 has been identified in the genome of patients with atypical myeloproliferative neoplasms.
• The simplest model as to how these rearrangements occur is through the simultaneous fragmentation of distinct chromosomal regions (breakpoints show a non-random distribution) and then subsequent imperfect reassembly by DNA repair pathways or aberrant DNA replication mechanisms.
• Strand-seq overcomes limitations of methods based on whole genome amplification for genetic variant calling: Since Strand-seq does not require reads (or read pairs) transversing the boundaries (or breakpoints) of CNVs or copy-balanced structural variant classes, it is less susceptible to common artefacts of single-cell methods based on whole genome amplification, which include variant calling dropouts due to missing reads at the variant breakpoint and read chimera.

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