scholarly journals Clinical Value for Diagnosis and Prognosis of Signal Sequence Receptor 1 (SSR1) and Its Potential Mechanism in Hepatocellular Carcinoma: A Comprehensive Study Based on High-Throughput Data Analysis

2021 ◽  
Vol Volume 14 ◽  
pp. 7435-7451
Author(s):  
Liang Chen ◽  
Yunhua Lin ◽  
Guoqing Liu ◽  
Rubin Xu ◽  
Yiming Hu ◽  
...  
2020 ◽  
Author(s):  
Erfan Sharifi ◽  
Niusha Khazaei ◽  
Nicholas Kieran ◽  
Sahel Jahangiri Esfahani ◽  
Abdulshakour Mohammadnia ◽  
...  

Author(s):  
Andreas Quandt ◽  
Sergio Maffioletti ◽  
Cesare Pautasso ◽  
Heinz Stockinger ◽  
Frederique Lisacek

Proteomics is currently one of the most promising fields in bioinformatics as it provides important insights into the protein function of organisms. Mass spectrometry is one of the techniques to study the proteome, and several software tools exist for this purpose. The authors provide an extendable software platform called swissPIT that combines different existing tools and exploits Grid infrastructures to speed up the data analysis process for the proteomics pipeline.


Gene ◽  
2021 ◽  
pp. 146111
Author(s):  
Erfan Sharifi ◽  
Niusha Khazaei ◽  
Nicholas W. Kieran ◽  
Sahel Jahangiri Esfahani ◽  
Abdulshakour Mohammadnia ◽  
...  

2013 ◽  
Vol 2013 ◽  
pp. 1-11 ◽  
Author(s):  
Dongmei Li ◽  
Timothy D. Dye

Resampling-based multiple testing procedures are widely used in genomic studies to identify differentially expressed genes and to conduct genome-wide association studies. However, the power and stability properties of these popular resampling-based multiple testing procedures have not been extensively evaluated. Our study focuses on investigating the power and stability of seven resampling-based multiple testing procedures frequently used in high-throughput data analysis for small sample size data through simulations and gene oncology examples. The bootstrap single-step minPprocedure and the bootstrap step-down minPprocedure perform the best among all tested procedures, when sample size is as small as 3 in each group and either familywise error rate or false discovery rate control is desired. When sample size increases to 12 and false discovery rate control is desired, the permutation maxTprocedure and the permutation minPprocedure perform best. Our results provide guidance for high-throughput data analysis when sample size is small.


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