Difference between revisions of "Ngs-pipeline"

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m (Text replace - "Personal genomics" to "Personalised medicine")
 
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{{Bioinformatics application
 
{{Bioinformatics application
 
|sw summary=Complete solution for human re-sequencing projects
 
|sw summary=Complete solution for human re-sequencing projects
|bio domain=Personal genomics, regulatory genomics epigenomics,
+
|bio domain=Personalised medicine, Epigenomics, Structural variation, Indel detection, SNP detection,  
|bio method=Read mapping, and SNP/INDEL discovery, structural variation discovery, regulatory element annotation
+
|bio method=Read mapping, Sequence annotation,
 
|bio tech=Illumina, ABI SOLiD,
 
|bio tech=Illumina, ABI SOLiD,
 
|created by=Denis Reshetov
 
|created by=Denis Reshetov

Latest revision as of 20:06, 19 December 2015

Application data

Created by Denis Reshetov
Biological application domain(s) Personalised medicine, Epigenomics, Structural variation, Indel detection, SNP detection
Principal bioinformatics method(s) Read mapping, Sequence annotation
Technology Illumina, ABI SOLiD
Created at VIGG RAS
Maintained? Yes
Input format(s) BAM, (Compressed) FASTQ, FASTQ, CSFASTA/CSQUAL (ABI SOLiD)
Output format(s) BAM, VCF
Programming language(s) Perl
Licence GPLv3
Operating system(s) Linux

Summary: Complete solution for human re-sequencing projects

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Description

Complete solution for human re-sequencing projects.





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References

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