The Role Of Collaborative Scholarship In The Mentorship Of Doctoral Students

The work of a professor is the “scholarship of teaching” (Boyer, 1990).  The strength of the teaching and learning environment is fostered by a dynamic interplay between the mentor (scholar) and the mentee (student).  Boyer (1990) suggests that in order to be a scholar, one must have “a recognition that knowledge is acquired through research, through synthesis, through practice, and through teaching.” However, as the academy has placed increased emphasis on research productivity as a concrete measure of scholarship, faculty may lose sight of what it means to view teaching as a scholarship. For example, if mentorship collaborations (student/faculty, faculty/faculty) are not viewed as scholarship activities, faculty may limit the amount or depth of student mentorship or peer collaborations to pursue their own research endeavors and thereby compromise the scholarship of teaching. Research is needed to gain an understanding of how faculties view collaborative research in relation to the scholarship of teaching.  The purpose of this paper is to first briefly describe the student-centered mentorship model for doctoral students proposed by Zipp and Olson (2008); second, to address the question, “Should the outcomes associated with this model be recognized as faculty scholarship?”; and third, to present pilot data of faculty perceptions on the role of collaborative scholarship in the mentorship of doctoral students

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