The availability, functionality, and quality of mobile applications supporting medication self-management

To systematically review mobile applications currently available to patients to support outpatient medication self-management

Satori 2017

The Satori is a student literary publication that expresses the artistic spirit of the students of Winona State University. Student poetry, prose, and graphic art are published in the Satori every spring since 1970. The Satori 2017 editors are: Editor-in-Chief: Sajda Omar Poetry Editor: Karl Hanson Art/Design Editor: Danielle Eberhard Prose Editor: Cassie Douglas Poetry Committee: Kelly Johnson and Lydia Papenfuss Art/Design Committee: Aurie Brighton and Xinyue Wang Prose Committee: Katie McCoy, Madison Wilke, Megan Back, Alayna Godfrey, Madelyn Hall, and Sam Stormoen Faculty Advisor: Dr. Gary Eddy, Professor of Englishhttps://openriver.winona.edu/satori/1013/thumbnail.jp

Finishing the euchromatic sequence of the human genome

The sequence of the human genome encodes the genetic instructions for human physiology, as well as rich information about human evolution. In 2001, the International Human Genome Sequencing Consortium reported a draft sequence of the euchromatic portion of the human genome. Since then, the international collaboration has worked to convert this draft into a genome sequence with high accuracy and nearly complete coverage. Here, we report the result of this finishing process. The current genome sequence (Build 35) contains 2.85 billion nucleotides interrupted by only 341 gaps. It covers ∼99% of the euchromatic genome and is accurate to an error rate of ∼1 event per 100,000 bases. Many of the remaining euchromatic gaps are associated with segmental duplications and will require focused work with new methods. The near-complete sequence, the first for a vertebrate, greatly improves the precision of biological analyses of the human genome including studies of gene number, birth and death. Notably, the human enome seems to encode only 20,000-25,000 protein-coding genes. The genome sequence reported here should serve as a firm foundation for biomedical research in the decades ahead

Stepwise regression model.

(XLSX)</p

Factors predicting knowing <i>SMN2</i> copy number.

Factors predicting knowing SMN2 copy number.</p

Open-ended supplement: Demographics of respondents diagnosed through muscle biopsy.

Open-ended supplement: Demographics of respondents diagnosed through muscle biopsy.</p

Traditional SMA classification [1].

Traditional SMA classification [1].</p

Open-ended supplement: Diagnostic methods information^a.

Open-ended supplement: Diagnostic methods informationa.</p