Difference between revisions of "PerM"
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| − | [[Category:Software]][[Category:NGS]][[Category: | + | [[Category:Software]][[Category:NGS]][[Category:Biology]][[Category:Mapping]] |
{|<!--CONFIGURATION: REQUIRED--> | {|<!--CONFIGURATION: REQUIRED--> | ||
|{{#vardefine:app|perm}} | |{{#vardefine:app|perm}} | ||
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PerM is a software package which was designed to perform highly efficient genome scale alignments for hundreds of millions of short reads produced by the ABI SOLiD and Illumina sequencing platforms. Today PerM is capable of providing full sensitivity for alignments within 4 mismatches for 50bp SOLID reads and 9 mismatches for 100bp Illumina reads. | PerM is a software package which was designed to perform highly efficient genome scale alignments for hundreds of millions of short reads produced by the ABI SOLiD and Illumina sequencing platforms. Today PerM is capable of providing full sensitivity for alignments within 4 mismatches for 50bp SOLID reads and 9 mismatches for 100bp Illumina reads. | ||
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<!--Modules--> | <!--Modules--> | ||
| − | + | ==Environment Modules== | |
| − | + | Run <code>module spider {{#var:app}}</code> to find out what environment modules are available for this application. | |
| − | + | ==System Variables== | |
| − | <!-- | + | * HPC_{{uc:{{#var:app}}}}_DIR - installation directory |
| − | {{#if: {{#var: exe}}|== | + | <!--Additional--> |
| + | {{#if: {{#var: exe}}|==Additional Information== | ||
The reference sequence(s) can be whole genomes with multiple chromosomes, the transcriptome or even the millions reads in the fasta format, separated by '>'. The reads can be in the fasta, fastq, csfasta + QUAL formats or fastq for SOLiD reads. PerM can output alignments in our mapping format or the SAM format and that output can be further processed by ComB, SAMtools, RseqFlow pipeline and the [[Galaxy]]. Check the [http://code.google.com/p/perm/wiki/Manual manual] for more detail. | The reference sequence(s) can be whole genomes with multiple chromosomes, the transcriptome or even the millions reads in the fasta format, separated by '>'. The reads can be in the fasta, fastq, csfasta + QUAL formats or fastq for SOLiD reads. PerM can output alignments in our mapping format or the SAM format and that output can be further processed by ComB, SAMtools, RseqFlow pipeline and the [[Galaxy]]. Check the [http://code.google.com/p/perm/wiki/Manual manual] for more detail. | ||
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See the [[{{PAGENAME}}_PBS]] page for {{#var: app}} PBS script examples.|}} | See the [[{{PAGENAME}}_PBS]] page for {{#var: app}} PBS script examples.|}} | ||
<!--Policy--> | <!--Policy--> | ||
| − | {{#if: {{#var: policy}}|==Usage | + | {{#if: {{#var: policy}}|==Usage Policy== |
WRITE USAGE POLICY HERE (perhaps templates for a couple of main licensing schemes can be used) | WRITE USAGE POLICY HERE (perhaps templates for a couple of main licensing schemes can be used) | ||
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Latest revision as of 17:40, 21 August 2022
Description
PerM is a software package which was designed to perform highly efficient genome scale alignments for hundreds of millions of short reads produced by the ABI SOLiD and Illumina sequencing platforms. Today PerM is capable of providing full sensitivity for alignments within 4 mismatches for 50bp SOLID reads and 9 mismatches for 100bp Illumina reads.
Environment Modules
Run module spider perm to find out what environment modules are available for this application.
System Variables
- HPC_PERM_DIR - installation directory
Additional Information
The reference sequence(s) can be whole genomes with multiple chromosomes, the transcriptome or even the millions reads in the fasta format, separated by '>'. The reads can be in the fasta, fastq, csfasta + QUAL formats or fastq for SOLiD reads. PerM can output alignments in our mapping format or the SAM format and that output can be further processed by ComB, SAMtools, RseqFlow pipeline and the Galaxy. Check the manual for more detail.
Two binaries are available - PerM and PerM-OMP (OpenMP multi-threaded version).