Changes between Version 1 and Version 2 of SOPs/genome_regions_annotations
- Timestamp:
- 03/29/13 14:44:42 (12 years ago)
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SOPs/genome_regions_annotations
v1 v2 99 99 === Method 3 (for SNPs, using snpEff) === 100 100 101 * This takes SNP positions as input . I don't think it works on regions > 1 nt.101 * This takes SNP positions as input (in VCF format). I don't think it works on regions > 1 nt. 102 102 * This method has the advantage that it can link SNPs to synonymous and nonsynonymous codons to identify changed in encoded protein. 103 103 * The [[http://snpeff.sourceforge.net/|snpEff web site]] has lots of information. … … 108 108 {{{ 109 109 # Default output based on Ensembl gene annotation 110 snpEff hg 37.61 snps.calls1> snps.calls.out.txt 2> snps.calls.err.txt110 snpEff hg19 < snps.calls.vcf 1> snps.calls.out.txt 2> snps.calls.err.txt 111 111 # Default output based on UCSC gene annotation 112 snpEff hg 37 snps.calls1> snps.calls.out.txt 2> snps.calls.err.txt112 snpEff hg19 < snps.calls.vcf 1> snps.calls.out.txt 2> snps.calls.err.txt 113 113 }}} 114 114 115 115 {{{ 116 116 # Don't show so much stuff 117 snpEff -no-downstream -no-intergenic -no-intron -no-upstream hg 37.61 snps.calls1> snps.calls.filt.out.txt 2> snps.calls.filt.err.txt117 snpEff -no-downstream -no-intergenic -no-intron -no-upstream hg19 < snps.calls.vcf 1> snps.calls.filt.out.txt 2> snps.calls.filt.err.txt 118 118 }}} 119 120 On Whitehead servers, pre-installed genomes (with annotations) can be chosen from the directory names in /usr/local/share/snpEff/data