𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A specification-based functional testing method for JSP designed programs

✍ Scribed by RMF Roper; P Smith


Publisher
Elsevier Science
Year
1988
Tongue
English
Weight
910 KB
Volume
30
Category
Article
ISSN
0950-5849

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


A method for extraction of function modu
✍ Satoshi Nakamura; Yasutaka Fujimoto πŸ“‚ Article πŸ“… 2009 πŸ› Wiley (John Wiley & Sons) 🌐 English βš– 373 KB

## Abstract In this paper, a method to extract function modules from sequential control programs is proposed. A hierarchical structure of a given sequential program can be found by using association graph. If some or more variables are connected to each other (strongly connected), the layered struc

A Microcomputer Program for the Design a
✍ E. Bellissant; J. Benichou; Cl. Chastang πŸ“‚ Article πŸ“… 1994 πŸ› Elsevier Science 🌐 English βš– 470 KB

We developed an interactive and menu-driven computer program to help investigators design and analyze phase II cancer clinical trials with a group sequential method, namely the sequential probability ratio test or the triangular test. Based on the values selected for the parameters of the trial, the

POBASCAM, a population-based randomized
✍ Nicole W.J. Bulkmans; Lawrence Rozendaal; Peter J.F. Snijders; Feja J. Voorhorst πŸ“‚ Article πŸ“… 2004 πŸ› John Wiley and Sons 🌐 French βš– 253 KB πŸ‘ 2 views

## Abstract Cytological cervical screening is rather inefficient because of relatively high proportions of false negative and false positive smears. To evaluate the efficiency of high‐risk human papillomavirus (hrHPV) testing, by GP5+/6+ PCR‐enzyme immunoassay (EIA), in conjunction with cytology (I

Comparison of various density functional
✍ Keith W. Wiitala; Christopher J. Cramer; Thomas R. Hoye πŸ“‚ Article πŸ“… 2007 πŸ› John Wiley and Sons 🌐 English βš– 295 KB

## Abstract Full ^1^H and ^13^C NMR chemical shift assignments were made for two sets of penam β‐lactams: namely, the diastereomeric (2__S__, 5__S__, 6__S__)‐, (2__S__, 5__R__, 6__R__)‐, (2__S__, 5__S__, 6__R__)‐, and (2__S__, 5__R__, 6__S__)‐methyl 6‐(1,3‐dioxoisoindolin‐2‐yl)‐3,3‐dimethyl‐7‐oxo‐4