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*bcftools filter | |
*Filter variants per region (in this example, print out only variants mapped to chr1 and chr2) | |
qbcftools filter -r1,2 ALL.chip.omni_broad_sanger_combined.20140818.snps.genotypes.hg38.vcf.gz | |
*printing out info for only 2 samples: | |
bcftools view -s NA20818,NA20819 filename.vcf.gz | |
*printing stats only for variants passing the filter: | |
bcftools view -f PASS filename.vcf.gz |
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#!/usr/bin/env perl | |
use v5.10; | |
use strict; | |
use warnings; | |
use Carp; | |
use IO::Prompt::Tiny 'prompt'; | |
use Net::GitHub; | |
use Path::Tiny; | |
use RT::Client::REST::Ticket; | |
use RT::Client::REST; |
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#!/usr/bin/perl | |
use strict; | |
use warnings; | |
use Bio::DB::EUtilities; | |
# this needs to be a list of EntrezGene unique IDs | |
my @ids = @ARGV; | |
my $eutil = Bio::DB::EUtilities->new(-eutil => 'esearch', | |
-email => '[email protected]', |