Email-Set Visualization: Facilitating Re-Finding in Email Archives

In this paper we describe ESVT – EmailSet Visualization Tool, an email archive tool that provides users a visualization to re-find and discover information in their email archive. ESVT is an end-to-end email archive tool that can be used from archiving a user’s email messages to visualizing queries on the email archive. We address email archiving by allowing import of email messages from an email server or from a standard existing email client. The central idea in ESVT’s visualization, an “email-set”, is the set of emails that are the result of a query on a user’s email archive. ESVT provides a multiple email-set view - visualization of multiple email-sets on a time axis. In addition, each email set can be individually visualized based on person and time axis, using the single email-set view. Query logs, individual email visualization, multiple email set visualization provide rich contextual cues, thus enabling end users to deal with email overload and re-find past email which otherwise wouldn’t be discovered easily

Why High Leverage is Optimal for Banks

Abstract Liquidity production is a central role of banks. High leverage is optimal for banks in a capital structure model in which there is a market premium for (socially valuable) liquid financial claims and no deviations fro

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