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| + | '''Note:''' the latest version of this practical is available at: [[SeqShop: Analysis of Structural Variation Practical]] |
| + | * The ones here is the original one from the June workshop (updated to be run from elsewhere) |
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| == Goals of This Session == | | == Goals of This Session == |
| * What we want to learn is calling large deletions using GenomeSTRiP implemented in [[GotCloud]] pipeline | | * What we want to learn is calling large deletions using GenomeSTRiP implemented in [[GotCloud]] pipeline |
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| <div class="mw-collapsible-content"> | | <div class="mw-collapsible-content"> |
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− | This tutorial builds on the alignment tutorial, if you have not already, please first run that tutorial: [[SeqShop:_Sequence_Mapping_and_Assembly_Practical|Alignment Tutorial]] | + | This tutorial builds on the alignment tutorial, if you have not already, please first run that tutorial: [[SeqShop:_Sequence_Mapping_and_Assembly_Practical, June 2014|Alignment Tutorial]] |
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− | It also uses the bam.index file created in the SnpCall Tutorial. If you have not yet run that tutorial, please follow the directions at: [[SeqShop:_Variant_Calling_and_Filtering_for_SNPs_Practical#GotCloud_BAM_Index_File|GotCloud BAM Index File]] | + | It also uses the bam.index file created in the SnpCall Tutorial. If you have not yet run that tutorial, please follow the directions at: [[SeqShop:_Variant_Calling_and_Filtering_for_SNPs_Practical, June 2014#GotCloud_BAM_Index_File|GotCloud BAM Index File]] |
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| * BAMs->SVs rather than BAMs->SNPs | | * BAMs->SVs rather than BAMs->SNPs |
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− | If you want a reminder, of what they look like, here is a link to the previous tutorial : [[SeqShop:_Variant_Calling_and_Filtering_for_SNPs_Practical#Examining_GotCloud_SnpCall_Input_files|GotCloud SnpCall Input Files]] | + | If you want a reminder, of what they look like, here is a link to the previous tutorial : [[SeqShop:_Variant_Calling_and_Filtering_for_SNPs_Practical, June 2014#Examining_GotCloud_SnpCall_Input_files|GotCloud SnpCall Input Files]] |
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| If you want to check if you still have the bam index file, run | | If you want to check if you still have the bam index file, run |
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| We will use the same configuration file we used for the GotCloud Align tutorial. | | We will use the same configuration file we used for the GotCloud Align tutorial. |
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− | See [[SeqShop:_Sequence_Mapping_and_Assembly_Practical#GotCloud Configuration File|SeqShop: Alignment: GotCloud Configuration File]] for more details | + | See [[SeqShop:_Sequence_Mapping_and_Assembly_Practica, June 2014l#GotCloud Configuration File|SeqShop: Alignment: GotCloud Configuration File]] for more details |
| * Note we want to limit snpcall to just chr22 so the configuration already has <code>CHRS = 22</code> (default was 1-22 & X). | | * Note we want to limit snpcall to just chr22 so the configuration already has <code>CHRS = 22</code> (default was 1-22 & X). |
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| In principle, the metadata can be created from the input BAM files by running the following command | | In principle, the metadata can be created from the input BAM files by running the following command |
− | #time perl ${SS}/svtoolkit/bin/genomestrip.pl -run-metadata --conf ${SS}/gotcloud.conf --numjobs 2 --base-prefix ${SS} --outdir ${OUT} | + | perl ${SS}/svtoolkit/bin/genomestrip.pl -run-metadata --conf ${SS}/gotcloud.conf --numjobs 2 --base-prefix ${SS} --outdir ${OUT} |
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| '''WAIT!!!!! DO NOT RUN THIS COMMAND, because it will take ~50 minutes to finish'''. | | '''WAIT!!!!! DO NOT RUN THIS COMMAND, because it will take ~50 minutes to finish'''. |