Search Results for "pairwise comparison"

Prometheus-Eval is an open-source framework designed to evaluate the outputs of large language models using specialized evaluator models known as Prometheus. The project provides tools, datasets, and scripts that allow developers and researchers to measure the quality of LLM responses through automated scoring rather than relying solely on human evaluators. It implements an “LLM-as-a-judge” approach in which a dedicated language model analyzes instruction–response pairs and assigns scores or...

...We anticipate that the high accuracy and reproducibility of miniABS may provide a SSP at a low cost, as well as providing a platform for cross comparison among gene expression datasets generated with different technical platforms.

...Please cite this if you find it useful:- Siraj, S., Mikhailov, L. and Keane, J. A. (2015), "PriEsT: an interactive decision support tool to estimate priorities from pairwise comparison judgments". International Transactions in Operational Research. 22: 217–235. doi:10.1111/itor.12054

CUDAlign is a tool able to align pairwise DNA sequences of unrestricted size in CUDA GPUs, using the Smith-Waterman algorithm combined with Myers-Miller. It produces the optimal alignment of 1 million base sequences in 45 seconds using a GTX 560 Ti. Many optimizations are being developed for this software. Look at the following papers for detailed information: [1] Edans Sandes, Alba Melo.

****Download zip file and run setup.exe**** This application facilitates the compilation of pairwise comparisons (To learn more visit http://deseng.ryerson.ca/~fil/t/pwisecomp.html). Traditionally done in an Excel document, pairwise comparisons can be painstaking and time consuming to put together. This application aims the make this process easier through a user friendly interface and special tools. In addition to being able to manually add entries to a given comparison, users can directly add them be selecting an appropriate excel sheet that has been filled out. ...

...It also creates "difference" alignments from regular ones (and vice-versa). It can handle gaps and ambiguities in different ways. Gaps can be: - all used; - all ignored; - ignored only at the ends of the sequences, in a pairwise manner; - ignored only at the ends, but now globally (in effect trimming the whole alignment to the farthest sequences from the ends). Ambiguities (things like R, Y, N, W, etc. in a DNA sequence) can be treated like: - consider ambiguities as always different; - consider ambiguity as partially different (e.g. R would be 0.5 different from A or G); - ignore ambiguities in each pairwise comparison; - remove all columns, globally, that show any ambiguity. ...