Package: idemuxcpp
Version: 0.1.7-1
Architecture: amd64
Maintainer: Lexogen <gregor.entzian@lexogen.com>
Installed-Size: 12220
Depends: libboost-filesystem1.67.0, libboost-iostreams1.67.0, libboost-system1.67.0, libc6 (>= 2.14), libgcc1 (>= 1:3.0), libgomp1 (>= 4.9), libstdc++6 (>= 6), 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: 1206528
MD5sum: 68485d3d037ec9cfe04a70d4fa0cf595
SHA1: 3c791779d99c1c619e2e598e4bfca7dee5059e45
SHA256: 40d3ca77b39c3fa422d583469f81114d918e5e2952ed576f45111a5159ea0c82
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.