ZVT是对fooltrader重新思考后编写的量化项目，其包含可扩展的数据recorder，api，因子计算，选股，回测，交易,以及统一的可视化，定位为中低频 多级别 多因子 多标的 全市场分析和交易框架。
Pipeline solution to support building, deploying and automating any software project on Kunpeng Architecture
Confidential computing framework for iTrustee OS normal world client
Confidential computing framework for developing TA on itrustee OS
Confidential computing framework for iTrustee OS driver
Kunpeng Porting Advisor is an application porting tool developers, user, and independent software vendors(ISVs) of the Kunpeng platform.
C++ API repodesc command-line toolkit for working with BAM data
A comprehensive library of analysis tools for FMRI, MRI and DTI brain imaging data
NEMO: Nucleus for European Modelling of the Ocean is a state-of-the-art modelling framework for research activities and forecasting services in ocean and climate sciences
OpenCV (Open Source Computer Vision Library: http://opencv.org) is an open-source library that includes several hundreds of computer vision algorithms.
A set of tools developed for visualization and processing of long-read sequencing data from Oxford Nanopore Technologies and Pacific Biosciences.
FigTree is designed as a graphical viewer of phylogenetic trees and as a program for producing publication-ready figures.
deepTools: tools for exploring deep sequencing data.
Manta calls structural variants (SVs) and indels from mapped paired-end sequencing reads. It is optimized for analysis of germline variation in small sets of individuals and somatic variation in tumor/normal sample pairs. Manta discovers, assembles and scores large-scale SVs, medium-sized indels and large insertions within a single efficient workflow. The method is designed for rapid analysis on standard compute hardware: NA12878 at 50x genomic coverage is analyzed in less than 20 minutes on a 20 core server, and most WGS tumor/normal analyses can be completed within 2 hours. Manta combines paired and split-read evidence during SV discovery and scoring to improve accuracy, but does not require split-reads or successful breakpoint assemblies to report a variant in cases where there is strong evidence otherwise. It provides scoring models for germline variants in small sets of diploid samples and somatic variants in matched tumor/normal sample pairs. There is experimental support for analysis of unmatched tumor samples as well (see details below). Manta accepts input read mappings from BAM or CRAM files and reports all SV and indel inferences in VCF 4.1 format.
