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Name: Believer
Type: User
Company: Sun Yat-sen University
Bio: A graduate of bioinformatics
Location: Guangzhou, China
Believer's Projects
-chanlun
文件 笔和线段的一种划分.py,只需要把k线high，low数据输入，就能自动实现笔，线段，中枢，买卖点，走势类型的划分了。可以把sh.csv 作为输入文件。个人简历见.pdf。时间的力量。有人说择时很困难，有人说选股很容易，有人说统计套利需要的IT配套设施很重要。还有人说系统有不可测原理。众说纷纭。分布式的系统，当你的影响可以被忽略，你才能实现，Jiang主席所谓之，闷声发大财。第一周，大盘跌了1%，挣钱了一万，挣了5%。 #股票 #股市 #缠论 https://v.kuaishou.com/bFEl6M Copy this message and open 【Kwai】to view!
archon
PHP Data Analysis Framework
auto-task-helper
依赖于Auto.js(Android)，自动化执行双十一电商们的任务
best-readme-template
An awesome README template to jumpstart your projects!
bioinformatic-master-codes
Repository for codes written during my bioinformatic master.
birthdayreminder
应用Python代码进行快捷方便的每日生日提醒(通过微信Server酱服务号消息推送)
c-cap
C语言程序设计CAP课程代码
code-notebook
Help with memorizing some code caveats and specific usages. Some of these were migrated from my OneNote app.
coder2gwy
互联网首份程序员考公指南，由3位已经进入体制内的前大厂程序员联合献上。
computer-maintanence
Maintanence record for personal computer and lab server
daily-code-record
Record daily simple code.
data-analysis-projects
A collection of various data analysis projects.
data-structure-and-algorithm
菜鸟的数据结构与算法成长之路
ebf_contribute_guide
如何参与野火项目（how to contribute）
gdc-maf-tool
Easy GDC MAF file concatenation
gdc-tsv-tool
Metadata in TSV format for GDC files
igv
Integrative Genomics Viewer. Fast, efficient, scalable visualization tool for genomics data and annotations
machine-learning-study-path-march-2019
A complete ML study path, focused on TensorFlow and Scikit-Learn
markdown-resume
⭐️ Markdown 简历模版
markdown-website-demonstration
A self-written vue module to display markdown alongwith its menu in side-bar
pmgshare
PMG lab code sharing
pta
中M2018春C入门和进阶练习集
py_reminder
This is a Python decorator sending email notification on your task progress
python_interview_question
关于python的面试题
radia
RADIA: RNA and DNA Integrated Analysis for Somatic Mutation Detection
record-for-bioinformatic-data-processing
记录琐碎但必不可少的数据处理过程，避免日后需要重现时难以找到
rna-ssnv
RNA-SSNV: A reliable Somatic Single Nucleotide Variants identification framework for RNA-seq data.
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