Package: idemuxcpp
Version: 0.1.7-1
Architecture: amd64
Maintainer: Lexogen <gregor.entzian@lexogen.com>
Installed-Size: 12212
Depends: libboost-filesystem1.55.0, libboost-iostreams1.55.0, libboost-system1.55.0, libc6 (>= 2.14), libgcc1 (>= 1:4.1.1), libgomp1 (>= 4.9), libstdc++6 (>= 4.9), zlib1g (>= 1:1.1.4), zlib1g-dev (>= 1.2.8), libboost-dev (>= 1.55), libboost-filesystem-dev (>= 1.55), libboost-system-dev (>= 1.55), libboost-iostreams-dev (>= 1.55)
Conflicts: idemuxcpp
Provides: idemuxcpp
Filename: ./amd64/idemuxcpp_0.1.7-1_amd64.deb
Size: 933186
MD5sum: 1fcb660cdd9b6100e7e670591dac5c1c
SHA1: d2e20a20bd818745aee9a55d47ed12c8292c96d9
SHA256: 72f7012b3c2233d58739c3be2e41a51b5ba0c53a83c5f3df71c8dd6703933d2e
Section: science
Priority: optional
Description: Demultiplex RNA-seq reads from fastq.gz files into separate files according to their indices.
 Idemux can demultiplex based on i7, i5, and i1 inline barcodes. While this tool
 can generally be used to demultiplex any barcodes (as long as they are
 correctly supplied and in the fastq header), it performs best when used in
 combination with Lexogen indices, as it will correct common sequencing errors
 in the sequenced barcodes. This will allow you to retain more reads from your
 sequencing experiment while minimizing cross contamination.

Package: idemuxcpp
Version: 0.1.7-1
Architecture: i386
Maintainer: Lexogen <gregor.entzian@lexogen.com>
Installed-Size: 12194
Depends: libboost-filesystem1.55.0, libboost-iostreams1.55.0, libboost-system1.55.0, libc6 (>= 2.4), libgcc1 (>= 1:4.1.1), libgomp1 (>= 4.9), libstdc++6 (>= 4.9), zlib1g (>= 1:1.1.4), zlib1g-dev (>= 1.2.8), libboost-dev (>= 1.55), libboost-filesystem-dev (>= 1.55), libboost-system-dev (>= 1.55), libboost-iostreams-dev (>= 1.55)
Conflicts: idemuxcpp
Provides: idemuxcpp
Filename: ./i386/idemuxcpp_0.1.7-1_i386.deb
Size: 934638
MD5sum: 378edf1befe6c711d29cf33faceaa19b
SHA1: 0d7039ecae0af7958186cb73868accf12dc69d2c
SHA256: 477b691b60d91366b52a2814aad3bb0c44211bc6779d928bdeb29b3bdecb02d0
Section: science
Priority: optional
Description: Demultiplex RNA-seq reads from fastq.gz files into separate files according to their indices.
 Idemux can demultiplex based on i7, i5, and i1 inline barcodes. While this tool
 can generally be used to demultiplex any barcodes (as long as they are
 correctly supplied and in the fastq header), it performs best when used in
 combination with Lexogen indices, as it will correct common sequencing errors
 in the sequenced barcodes. This will allow you to retain more reads from your
 sequencing experiment while minimizing cross contamination.