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academic/snpEff: Updated for version 4.3k.
Signed-off-by: David Spencer <idlemoor@slackbuilds.org>
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4 changed files with 9 additions and 9 deletions
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@ -14,11 +14,11 @@ acid changes).
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This also installs SnpSift, a toolbox that allows you to filter and
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manipulate annotated files. Once your genomic variants have been
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annotated, you need to filter them out in order to find the
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annotated, you need to filter them out in order to find the
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"interesting / relevant variants". Given the large data files, this is
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not a trivial task (e.g. you cannot load all the variants into XLS
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spreadsheet). SnpSift helps to perform this VCF file manipulation and
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filtering required at this stage in data processing pipelines.
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filtering required at this stage in data processing pipelines.
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If you are using SnpEff or SnpSift, please cite:
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A program for annotating and predicting the effects of single
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@ -13,7 +13,7 @@ snpEff: annotates and predicts the effects of variants on genes (such
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snpEff: as amino acid changes).
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snpEff:
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snpEff: Home: http://snpeff.sourceforge.net/
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snpEff: References: /usr/doc/snpEff-4.2/References
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snpEff: References: /usr/doc/snpEff-4.3k/References
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snpEff:
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snpEff:
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snpEff:
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@ -2,7 +2,7 @@
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# Slackware build script for snpEff
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# Copyright 2015-2016 Petar Petrov slackalaxy@gmail.com
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# Copyright 2015-2017 Petar Petrov slackalaxy@gmail.com
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# All rights reserved.
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#
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# Redistribution and use of this script, with or without modification, is
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@ -23,8 +23,8 @@
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# ADVISED OF THE POSSIBILITY OF SUCH DAMAGE.
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PRGNAM=snpEff
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VERSION=${VERSION:-4.2}
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SRCVER=${SRCVER:-v4_2}
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VERSION=${VERSION:-4.3k}
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SRCVER=${SRCVER:-v4_3k}
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BUILD=${BUILD:-1}
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TAG=${TAG:-_SBo}
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@ -1,8 +1,8 @@
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PRGNAM="snpEff"
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VERSION="4.2"
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VERSION="4.3k"
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HOMEPAGE="http://snpeff.sourceforge.net/"
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DOWNLOAD="http://sourceforge.net/projects/snpeff/files/snpEff_v4_2_core.zip"
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MD5SUM="25ae5b062d57072de6cfb8677ca3625a"
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DOWNLOAD="https://sourceforge.net/projects/snpeff/files/snpEff_v4_3k_core.zip"
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MD5SUM="2533b329c734a678780cf045ba6b4a48"
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DOWNLOAD_x86_64=""
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MD5SUM_x86_64=""
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REQUIRES="jdk"
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