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  1. ...sequence scaffolds and isolated contigs, a high-resolution HAPPY map was constructed (see Methods). A total of 173 markers (taken from the early chromosome-specific sequence reads or, later, from contigs of the assembly) were mapped to a single linkage group. Markers that failed to link to the remainder...
  2. ...showed an extreme bias in their distribution, most originating from the already known parts of the fragment (data not shown). However, the minority of the subclones which did fall within the gaps were HAPPY mapped at high resolution to produce dense local maps of the unsequenced regions (see Methods...
  3. .... Multigene amplification and massively parallel sequencing for cancer mutation discovery. Proc Natl Acad Sci 104: 9387–9392. DeAngelis MM, Wang DG, Hawkins TL. 1995. Solid-phase reversible immobilization for the isolation of PCR products. Nucleic Acids Res 23: 4742–4743. Dear PH, Cook PR. 1993. Happy mapping...
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