58 research outputs found
Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing
Although genetic lesions responsible for some mendelian disorders can be rapidly discovered through massively parallel sequencing of whole genomes or exomes, not all diseases readily yield to such efforts. We describe the illustrative case of the simple mendelian disorder medullary cystic kidney disease type 1 (MCKD1), mapped more than a decade ago to a 2-Mb region on chromosome 1. Ultimately, only by cloning, capillary sequencing and de novo assembly did we find that each of six families with MCKD1 harbors an equivalent but apparently independently arising mutation in sequence markedly under-represented in massively parallel sequencing data: the insertion of a single cytosine in one copy (but a different copy in each family) of the repeat unit comprising the extremely long (~1.5–5 kb), GC-rich (>80%) coding variable-number tandem repeat (VNTR) sequence in the MUC1 gene encoding mucin 1. These results provide a cautionary tale about the challenges in identifying the genes responsible for mendelian, let alone more complex, disorders through massively parallel sequencing.National Institutes of Health (U.S.) (Intramural Research Program)National Human Genome Research Institute (U.S.)Charles University (program UNCE 204011)Charles University (program PRVOUK-P24/LF1/3)Czech Republic. Ministry of Education, Youth, and Sports (grant NT13116-4/2012)Czech Republic. Ministry of Health (grant NT13116-4/2012)Czech Republic. Ministry of Health (grant LH12015)National Institutes of Health (U.S.) (Harvard Digestive Diseases Center, grant DK34854
Effects of the carrier frequency of interferential current on pain modulation in patients with chronic nonspecific low back pain: a protocol of a randomised controlled trial
Long Lamai community ICT4D E‐commerce system modelling: an agent oriented role‐based approach
This paper presents the post‐mortem report upon completion of the Long Lamai e‐commerce development project. Some weaknesses with regards to the current software modelling approach are identified and an alternative role‐based approach is proposed. We argue that the existing software modelling technique is not suitable for modelling, making it difficult to establish a good contract between stakeholders causing delays in the project delivery. The role‐based approach is able to explicitly highlight the responsibilities among stakeholders, while also forming the contract agreement among them leading towards sustainable ICT4D
Recommended from our members
Openness to Experience
As one of the five major personality traits, openness to experience has been established as a fundamental factor of personality. Yet its history, and what it constitutes, has not always been clear. This becomes obvious when observing how the label has changed over the decades: from Inquiring Intellect to Intelligence to Culture until finally the consensus of Openness to Experience. This final connotation denotes people who are flexible and receptive to all experiential possibilities. It is this flexibility that perhaps most defines open people and enables them to be creative, establish complex worldviews, and probe the depths of human experience. Therefore, open people not only see more possibilities but also engage with them. This chapter starts with a brief review of the history of openness to experience that leads into contemporary conceptualizations. It then moves on to discussing research on the trait’s associations with cognitive, perceptual, and behavioral outcomes. Finally, specific emphasis is placed on types of experience and how these may vary depending on people’s characteristics of openness to experience
- …
