An integrated pipeline for detection of de novo and rare inherited mutations from trios-based next-generation sequencing
An integrated pipeline for detection of de novo and rare inherited mutations from trios-based next-generation sequencing
mirTrios is developed by Beijing Institutes of Life Science, Chinese Academy of Sciences, Beijing, China
If you have any suggestions or comments to the mirTrios, the following address or e-mail can also be used.
Author members:
| Jinchen Li: | lijinchenbio@gmail.com |
| Tao Wang: | taowang2012bio@gmail.com |
| Yi Jiang: | jiangyi3029@foxmail.com |
| Huiqian Chen: | sara.chendmbi@gmail.com |
| Qing Xie: | peter_smith_bio@163.com |
| Qianzhi Shao: | shaozhi514@163.com |
| Xia Ran: | ranxia811@gmail.com |
| Kun Xia: | xiakun@sklmg.edu.cn |
| Zhongsheng Sun: | sunzs@mail.biols.ac.cn |
| Jinyu Wu: | wujy@mail.biols.ac.cn |
Project cooperation, project entrust, etc. Please connect Jinyu Wu.
| mirTools | It was developed to allow researchers to comprehensively characterize small RNA transcriptome. PubMed |
| MagicViewer | It is developed for deciphering the large-scale data generated from next-generation sequencing, which can easily visualize short read mapping, identify and annotate genetic variation based on the reference genome. PubMed |
| mirTools 2.0 | It is an updated version of mirTools 1.0, which is a comprehensive analysis strategy for non-coding RNA discovery, profiling, and functional annotation based on high-throughput sequencing. PubMed |
| RRBS-Analyser | A Comprehensive Web Server for Reduced Representation Bisulfite Sequencing Data Analysis. PubMed |
| NPdenovo | Neuropsychiatric Disorder De novo Mutation Database |
Copyright©2014, Beijing Institutes of Life Science, Chinese Academy of Sciences, Beijing, China.