Bioinfocyclopedia: E-learning with Jewel

Bioinfocyclopedia is created to spread up-to-date knowledge and hands-on training in different fields

0.11. SNP Analysis Workflow [Part4]

0.11. SNP Analysis Workflow [Part4]
0.10. SNP Analysis Workflow [Part3]

0.10. SNP Analysis Workflow [Part3]
0.9. SNP Analysis Workflow [Part2]

0.9. SNP Analysis Workflow [Part2]
0.8. SNP Analysis Workflow [Part1]

0.8. SNP Analysis Workflow [Part1]
0.7. Introduction: Importance and main reasons of exploring deleterious SNPs by in silico analysis

0.7. Introduction: Importance and main reasons of exploring deleterious SNPs by in silico analysis
0.6. Introduction: Different types of coding SNPs

0.6. Introduction: Different types of coding SNPs
4.2. Generating publication quality figure from merged summary SNP data using R

4.2. Generating publication quality figure from merged summary SNP data using R
0.5. Introduction: Different human genomic variants

0.5. Introduction: Different human genomic variants
0.4. Introduction: Human genomic variants

0.4. Introduction: Human genomic variants
0.3. Introduction: Reference human genome versions

0.3. Introduction: Reference human genome versions
0.2. Introduction: Reference human genome

0.2. Introduction: Reference human genome
0.1. Introduction: Human genome

0.1. Introduction: Human genome
10.2.2. Obtaining CHASMplus prediction result of SNPs using OpenCRAVAT

10.2.2. Obtaining CHASMplus prediction result of SNPs using OpenCRAVAT
10.1. Creating predefined and formatted input files for different servers from selected SNPs

10.1. Creating predefined and formatted input files for different servers from selected SNPs
9.5. Scoring and selection of SNPs from merged result file

9.5. Scoring and selection of SNPs from merged result file
9.4. Merging filtered and processed result files of different servers

9.4. Merging filtered and processed result files of different servers
9.3. Filtering and adding custom SNP ID to result files from different servers

9.3. Filtering and adding custom SNP ID to result files from different servers
9.2.2. Obtaining phyloP, phastCons and GERP++ conservation score of SNPs from dbNSFP database

9.2.2. Obtaining phyloP, phastCons and GERP++ conservation score of SNPs from dbNSFP database
9.2.1. Obtaining conservation score for amino acids of a protein from ConSurf server

9.2.1. Obtaining conservation score for amino acids of a protein from ConSurf server
9.1. Creating predefined and formatted input files for different servers from selected SNPs

9.1. Creating predefined and formatted input files for different servers from selected SNPs
8.5. Scoring and selection of SNPs from merged result file

8.5. Scoring and selection of SNPs from merged result file
8.4. Merging filtered and processed result files of different servers

8.4. Merging filtered and processed result files of different servers
8.3. Filtering and adding custom SNP ID to result files from different servers

8.3. Filtering and adding custom SNP ID to result files from different servers
8.2.2. Obtaining prediction result of SNPs from PredictSNP2 server

8.2.2. Obtaining prediction result of SNPs from PredictSNP2 server
8.2.1. Obtaining prediction result from M-CAP, REVEL, MetaLR, MetaRNN and BayesDel using dbNSFP

8.2.1. Obtaining prediction result from M-CAP, REVEL, MetaLR, MetaRNN and BayesDel using dbNSFP
8.2.3. Obtaining prediction result of SNPs from PredictSNP1 server

8.2.3. Obtaining prediction result of SNPs from PredictSNP1 server
8.1. Creating predefined and formatted input files for different servers

8.1. Creating predefined and formatted input files for different servers
7.3. Merging filtered and processed result files of different servers

7.3. Merging filtered and processed result files of different servers
7.4. Scoring and selection of SNPs from merged result file

7.4. Scoring and selection of SNPs from merged result file
7.2. Filtering and adding custom SNP ID to result files of different servers

7.2. Filtering and adding custom SNP ID to result files of different servers