Package: idemuxcpp
Version: 0.3.0-1
Architecture: amd64
Maintainer: Lexogen <gregor.entzian@lexogen.com>
Installed-Size: 27118
Depends: libboost-filesystem1.58.0, libboost-iostreams1.58.0, libboost-system1.58.0, libc6 (>= 2.14), libgcc1 (>= 1:3.0), libstdc++6 (>= 5.2), zlib1g (>= 1:1.2.2), zlib1g-dev (>= 1.2.8), libboost-dev (>= 1.55), libboost-filesystem-dev (>= 1.55), libboost-system-dev (>= 1.55), libboost-iostreams-dev (>= 1.55), libbamtools-dev (>= 2.3.0)
Conflicts: idemuxcpp
Provides: idemuxcpp
Filename: amd64/idemuxcpp_0.3.0-1_amd64.deb
Size: 2196628
MD5sum: aef10c8f9157a1807e4f44d6651c0126
SHA1: 5aeaec1c9d5ce3445e85a0c5ece6829c1e2fa1d2
SHA256: 2fe230d185c494cd7aecde5e1031a1d550e0b6b805cc64967bd94ae8d7d88120
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: 0.3.0-1
Architecture: i386
Maintainer: Lexogen <gregor.entzian@lexogen.com>
Installed-Size: 27112
Depends: libboost-filesystem1.58.0, libboost-iostreams1.58.0, libboost-system1.58.0, libc6 (>= 2.4), libgcc1 (>= 1:4.2), libstdc++6 (>= 5.2), zlib1g (>= 1:1.2.2), zlib1g-dev (>= 1.2.8), libboost-dev (>= 1.55), libboost-filesystem-dev (>= 1.55), libboost-system-dev (>= 1.55), libboost-iostreams-dev (>= 1.55), libbamtools-dev (>= 2.3.0)
Conflicts: idemuxcpp
Provides: idemuxcpp
Filename: i386/idemuxcpp_0.3.0-1_i386.deb
Size: 1968414
MD5sum: 29c8afb00ef8508ecc67edf61d2f818f
SHA1: 026bd4f8b8206963a0439292e4868172b2a96536
SHA256: bee82a555e2beb933576a4d7790307a1e7e39909f0a8e37589d3c0c35882b415
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.