scholarly journals SNPAAMapper: An efficient genome-wide SNP variant analysis pipeline for next-generation sequencing data

2013 ◽  
Vol 9 (17) ◽  
pp. 870-872 ◽  
Author(s):  
Yongsheng Bai ◽  
◽  
James Cavalcoli
Author(s):  
Chatzinikolaou Panagiotis ◽  
Makris Christos ◽  
Dimitrios Vlachakis ◽  
Sophia Kossida

In language of genetics and biochemistry, sequencing is the determination of an unbranched biopolymer's primary structure. A sequence is a symbolic linear depiction, result of sequencing. This sequence is a succinct summary of the most of the sequenced molecule's atomic-level structure. (Most known is DNA-sequencing, RNA-sequencing, Protein-sequencing and Next-Generation-sequencing)


2020 ◽  
Vol 41 (12) ◽  
pp. 2073-2077
Author(s):  
Daniel Lopez‐Lopez ◽  
Carlos Loucera ◽  
Rosario Carmona ◽  
Virginia Aquino ◽  
Josefa Salgado ◽  
...  

2017 ◽  
Author(s):  
Hyun-Hwan Jeong ◽  
Seon Young Kim ◽  
Maxime WC Rosseaux ◽  
Huda Y Zoghbi ◽  
Zhandong Liu

AbstractWe present a user-friendly, cloud-based, data analysis pipeline for the deconvolution of pooled screening data. This tool, termed SAVE for Screening Analysis Visual Explorer, serves a dual purpose of extracting, clustering and analyzing raw next generation sequencing files derived from pooled screening experiments while at the same time presenting them in a user-friendly way on a secure web-based platform. Moreover, SAVE serves as a useful web-based analysis pipeline for reanalysis of pooled CRISPR screening datasets. Taken together, the framework described in this study is expected to accelerate development of web-based bioinformatics tool for handling all studies which include next generation sequencing data. SAVE is available at http://save.nrihub.org.


Sign in / Sign up

Export Citation Format

Share Document